Inositol Lipids and Signal Transduction in the Nervous System: An Update
dc.contributor.author | Fisher, Stephen K. | en_US |
dc.contributor.author | Heacock, Anne M. | en_US |
dc.contributor.author | Agranoff, Bernard W. | en_US |
dc.date.accessioned | 2010-04-01T15:09:34Z | |
dc.date.available | 2010-04-01T15:09:34Z | |
dc.date.issued | 1992-01 | en_US |
dc.identifier.citation | Fisher, Stephen K.; Heacock, Anne M.; Agranoff, Bernard W. (1992). "Inositol Lipids and Signal Transduction in the Nervous System: An Update." Journal of Neurochemistry 58(1): 18-38. <http://hdl.handle.net/2027.42/65626> | en_US |
dc.identifier.issn | 0022-3042 | en_US |
dc.identifier.issn | 1471-4159 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/65626 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1309233&dopt=citation | en_US |
dc.description.abstract | The role that inositol lipids play in cellular signaling events in eukaryotic cells remains one of the most intensively investigated areas of cell biology. In this respect, phosphoinositide-mediated signal transduction in the CNS is no exception; major advances have been made since a previous review on this subject (Fisher and Agranoff, 1987). Not only have stimulated phosphoinositide turnover and its physiological sequelae been demonstrated repeatedly in a variety of neural preparations, but, in addition, the detailed molecular mechanisms underlying these events continue to unfold. Here we review the progress that has occurred in selected aspects of this topic since 1987. In the first two sections of this article, emphasis is placed on novel functional roles for the inositol lipids and on recent insights into the molecular characteristics and regulation of three key components of the phosphoinositide signal transduction system, namely, the inositol lipid kinases, phospholipases C (PLCs), and the inositol 1,4,5-trisphosphate[I(1,4,5)P 3 ] receptor. The metabolic fate of I(1,4,5)P 3 in neural tissues, as well as its control, is also detailed. Later we focus on identification of the multiple receptor subtypes that are coupled to inositol lipid turnover and discuss possible strategies for intervention into phosphoinositide-mediated signal transduction. Due to space limitations, an extensive evaluation of the diacylglycerol/protein kinase C (DAG/PKC) limb of the signal transduction pathway is not included (for reviews, see Nishizuka, 1988; Kanoh et al., 1990). | en_US |
dc.format.extent | 2475378 bytes | |
dc.format.extent | 3110 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.rights | 1992 International Society for Neurochemistry | en_US |
dc.title | Inositol Lipids and Signal Transduction in the Nervous System: An Update | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Neurosciences | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Neuroscience Laboratory, University of Michigan, Ann Arbor, Michigan, U.S.A. | en_US |
dc.contributor.affiliationum | * Department of Pharmacology, University of Michigan, Ann Arbor, Michigan, U.S.A. | en_US |
dc.contributor.affiliationum | Department of Biological Chemistry, University of Michigan, Ann Arbor, Michigan, U.S.A. | en_US |
dc.identifier.pmid | 1309233 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/65626/1/j.1471-4159.1992.tb09273.x.pdf | |
dc.identifier.doi | 10.1111/j.1471-4159.1992.tb09273.x | en_US |
dc.identifier.source | Journal of Neurochemistry | en_US |
dc.identifier.citedreference | Ackermann K. E., Gish B. G., Honchar M. P., and Sherman W. R. ( 1987 ) Evidence that inositol 1-phosphate in brain of lithium-treated rats results mainly from phosphatidylinositol metabolism. Biochem. J. 242, 517 – 524. | en_US |
dc.identifier.citedreference | Agranoff B. W. ( 1978 ) Cyclitol confusion. Trends Biochem. Sci. 3, N283 – N285. | en_US |
dc.identifier.citedreference | Agranoff B. W. and Fisher S. K. ( 1991 ) Phosphoinositides and their stimulated breakdown, in Inositol Phosphates and Related Compounds: Synthesis and Therapeutic Potential ( Reitz, A. B. ). Washington, D.C. American Chemical Society, pp. 20 – 32. | en_US |
dc.identifier.citedreference | Akil M. and Fisher S. K. ( 1989 ) Muscarinic receptor-stimulated phosphoinositide turnover in human SK-N-SH neuroblastoma cells: differential inhibition by agents that elevate cyclic AMP. J. Neurochem. 53, 1479 – 1486. | en_US |
dc.identifier.citedreference | Akins P. T., Surmeier D. J., and Kitai S. T. ( 1990 ) M 1 muscarinic acetylcholine receptor in cultured rat neostriatum regulates phosphoinositide hydrolysis. J. Neurochem. 54, 266 – 273. | en_US |
dc.identifier.citedreference | Akiyama K., Yamada N., and Otsuki S. ( 1989 ) Lasting increase in excitatory amino acid receptor-mediated polyphosphoinositide hydrolysis in the amygdala/pyriform cortex of amygdala-kindled rats. Brain Res. 485, 95 – 101. | en_US |
dc.identifier.citedreference | Alexander S. P. H., Kendall D. A., and Hill S. J. ( 1989 ) Differences in the adenosine receptors modulating inositol phosphates and cyclic AMP accumulation in mammalian cerebral cortex. Br. J. Pharmacol. 98, 1241 – 1248. | en_US |
dc.identifier.citedreference | Alexander S. P. H., Hill S. J., and Kendall D. A. ( 1990 ) Excitatory amino acid-induced formation of inositol phosphates in guinea-pig cerebral cortical slices: involvement of ionotropic or metabotropic receptors ? J. Neurochem. 55, 1439 – 1441. | en_US |
dc.identifier.citedreference | Allison J. H., Blisner M. E., Holland W. H., Hipps P. P., and Sherman W. R. ( 1976 ) Increased brain myo-inositol 1-phosphate in lithium-treated rats. Biochem. Biophys. Res. Commun. 71, 664 – 670. | en_US |
dc.identifier.citedreference | Allsup D. J. and Boarder M. R. ( 1990 ) Comparison of P 2 purinergic receptors of aortic endothelial cells with those of adrenal medulla: evidence for heterogeneity of receptor subtype and of inositol phosphate response. Mol. Pharmacol. 38, 84 – 91. | en_US |
dc.identifier.citedreference | Ambrosini A. and Meldolesi J. ( 1989 ) Muscarinic and quisqualate receptor-induced phosphoinositide hydrolysis in primary cultures of striatal and hippocampal neurons. Evidence for differential mechanisms of activation. J. Neurochem. 53, 825 – 833. | en_US |
dc.identifier.citedreference | Ananth U. S., Leli U., and Hauser G. ( 1987 ) Stimulation of phosphoinositide hydrolysis by serotonin in C 6 glioma cells. J. Neurochem. 48, 253 – 261. | en_US |
dc.identifier.citedreference | ArbonÉs L., Picatoste F., and GarcÍa A. ( 1988 ) Histamine H 1 -receptors mediate phosphoinositide hydrolysis in astrocyte-enriched primary cultures. Brain Res. 450, 144 – 152. | en_US |
dc.identifier.citedreference | Ashkenazi A., Ramachandran J., and Capon D. J. ( 1989 ) Acetylcholine analogue stimulates DNA synthesis in brain-derived cells via specific muscarinic receptor subtypes. Nature 340, 146 – 150. | en_US |
dc.identifier.citedreference | Baird J. G. and Nahorski S. R. ( 1990a ) Differences between muscarinic-receptor- and Ca 2+ -induced inositol polyphosphate isomer accumulation in rat cerebral-cortex slices. Biochem. J. 267, 835 – 838. | en_US |
dc.identifier.citedreference | Baird J. G. and Nahorski S. R. ( 1990b ) Quisqualate stimulates phosphoinositide metabolism by interaction with more than one receptor mechanism. Br. J. Pharmacol. (suppl.) 100, 315. | en_US |
dc.identifier.citedreference | Barrett R. W., Steffey M. E., and Wolfram C. A. W. ( 1989 ) Type-A cholecystokinin receptors in CHP212 neuroblastoma cells: evidence for association with G protein and activation of phosphoinositide hydrolysis. Mol. Pharmacol. 35, 394 – 400. | en_US |
dc.identifier.citedreference | Batty I. H. and Nahorski S. R. ( 1989 ) Rapid accumulation and sustained turnover of inositol phosphates in cerebral-cortex slices after muscarinic-receptor stimulation. Biochem. J. 260, 237 – 241. | en_US |
dc.identifier.citedreference | Baumgold J. and White T. ( 1989 ) Pharmacological differences between muscarinic receptors coupled to phosphoinositide turnover and those coupled to adenylate cyclase inhibition. Biochem. Pharmacol. 38, 1605 – 1616. | en_US |
dc.identifier.citedreference | Benjamins J. A. and Agranoff B. W. ( 1969 ) Distribution and properties of CDP-diglyceride: inositol transferase from brain. J. Neurochem. 16, 513 – 527. | en_US |
dc.identifier.citedreference | Berridge M. J. and Irvine R. F. ( 1989 ) Inositol phosphates and cell signalling. Nature 341, 197 – 205. | en_US |
dc.identifier.citedreference | Berridge M. J., Downes C. P., and Hanley M. R. ( 1982 ) Lithium amplifies agonist-dependent phosphatidylinositol responses in brain and salivary glands. Biochem. J. 206, 587 – 595. | en_US |
dc.identifier.citedreference | Blackstone C. D., Supattapone S., and Snyder S. H. ( 1989 ) Inositol-phospholipid-linked glutamate receptors mediate cerebellar parallel-fiber-Purkinje-cell synaptic transmission. Proc. Natl. Acad. Sci. USA 86, 4316 – 4320. | en_US |
dc.identifier.citedreference | Bleasdale J. E., Thakur N. R., Gremban R. S., Bundy G. L., Fitzpatrick F. A., Smith R. J., and Bunting S. ( 1990 ) Selective inhibition of receptor-coupled phospholipase C-dependent processes in human platelets and polymorphonuclear neutrophils. J. Pharmacol. Exp. Ther. 255, 756 – 768. | en_US |
dc.identifier.citedreference | Bonner T. I., Buckley N. J., Young A. C., and Brann M. R. ( 1987 ) Identification of a family of muscarinic acetylcholine receptor genes. Science 237, 527 – 532. | en_US |
dc.identifier.citedreference | Bonner T. I., Young A. C., Brann M. R., and Buckley N. J. ( 1988 ) Cloning and expression of the human and rat m5 muscarinic acetylcholine receptor genes. Neuron 1, 403 – 410. | en_US |
dc.identifier.citedreference | Boyer J. L., Hepler J. R., and Harden T. K. ( 1989 ) Hormone and growth factor receptor-mediated regulation of phospholipase C activity. Trends Pharmacol. Sci. 10, 360 – 364. | en_US |
dc.identifier.citedreference | Brooks P. A. and Spyer K. M. ( 1989 ) Investigation of inositol hexakisphosphate actions in rat nucleus tractus solitarius in vitro. Neurosci. Lett. 105, 120 – 124. | en_US |
dc.identifier.citedreference | Bunn S. J., Marley P. D., and Livett B. G. ( 1988 ) Effects of opioid compounds on basal and muscarinic induced accumulation of inositol phosphates in cultured bovine chromaffin cells. Biochem. Pharmacol. 37, 395 – 399. | en_US |
dc.identifier.citedreference | Burgess G. M., Mullaney I., McNeill M., Dunn P. M., and Rang H. P. ( 1989 ) Second messengers involved in the mechanism of action of bradykinin in sensory neurons in culture. J. Neurosci. 9, 3314 – 3325. | en_US |
dc.identifier.citedreference | Burnstock G. and Kennedy C. ( 1985 ) Is there a basis for distinguishing two types of P 2 -purinoceptor ? Gen. Pharmacol. 16, 433 – 440. | en_US |
dc.identifier.citedreference | Campbell M. D., Subramaniam S., Kotlikoff M. I., Williamson J. R., and Fluharty S. J. ( 1990 ) Cyclic AMP inhibits inositol polyphosphate production and calcium mobilization in neuroblastoma x glioma NG108-15 cells. Mol. Pharmacol. 38, 282 – 288. | en_US |
dc.identifier.citedreference | Carpenter C. L. and Cantley L. C. ( 1990 ) Phosphoinositide kinases. Biochemistry 29, 11147 – 11156. | en_US |
dc.identifier.citedreference | Carrithers M. D., Raman V. K., Masuda S., and Weyhenmeyer J. A. ( 1990 ) Effect of angiotensin II and III on inositol polyphosphate production in differentiated NG108-15 hybrid cells. Biochem. Biophys. Res. Commun. 167, 1200 – 1205. | en_US |
dc.identifier.citedreference | Carter H. R., Wallace M. A., and Fain J. N. ( 1990a ) Activation of phospholipase C in rabbit brain membranes by carbachol in the presence of GTPΓS; effects of biological detergents. Biochim. Biophys. Acta 1054, 129 – 135. | en_US |
dc.identifier.citedreference | Carter H. R., Wallace M. A., and Fain J. N. ( 1990b ) Purification and characterization of PLC-Β m, a muscarinic cholinergic regulated phospholipase C from rabbit brain membrane. Biochim. Biophys. Acta 1054, 119 – 128. | en_US |
dc.identifier.citedreference | Casebolt T. and Jope R. S. ( 1987 ) Chronic lithium treatment reduces norepinephrine-stimulated inositol phospholipid hydrolysis in rat cortex. Eur. J. Pharmacol. 140, 245 – 246. | en_US |
dc.identifier.citedreference | Challis R. A. J. and Nahorski S. R. ( 1990 ) Neurotransmitter and depolarization-stimulated accumulation of inositol 1,3,4,5-tetrakisphosphate mass in rat cerebral cortex slices. J. Neurochem. 54, 2138 – 2141. | en_US |
dc.identifier.citedreference | Challis R. A. J., Batty I. H., and Nahorski S. R. ( 1988 ) Mass measurements of inositol (1,4,5)trisphosphate in rat cerebral cortex slices using a radioreceptor assay: effects of neurotransmitters and depolarization. Biochem. Biophys. Res. Commun. 157, 684 – 691. | en_US |
dc.identifier.citedreference | Challis R. A. J., Chilvers E. R., Willcocks A. L., and Nahorski S. R. ( 1990 ) Heterogeneity of [ 3 H]inositol 1,4,5-trisphosphate binding sites in adrenal-cortical membranes. Biochem. J. 265, 421 – 427. | en_US |
dc.identifier.citedreference | Chan B. L., Chao M. V., and Saltiel A. R. ( 1989 ) Nerve growth factor stimulates the hydrolysis of glycosylphosphatidylinositol in PC-12 cells: a mechanism of protein kinase C regulation. Proc. Natl. Acad. Sci. USA 86, 1756 – 1760. | en_US |
dc.identifier.citedreference | Chen C.-K., Silverstein F. S., Fisher S. K., Statman D., and Johnson M. V. ( 1988 ) Perinatal hypoxic-ischemic brain injury enhances quisqualic acid-stimulated phosphoinositide turnover. J. Neurochem. 51, 353 – 359. | en_US |
dc.identifier.citedreference | Chiang C.-F. and Hauser G. ( 1989 ) Effects of bradykinin, GTPΓS, R59022 and N-ethylmaleimide on inositol phosphate production in NG108-15 cells. Biochem. Biophys. Res. Commun. 165, 175 – 181. | en_US |
dc.identifier.citedreference | Chiu A. S., Li P. P., and Warsh J. J. ( 1988 ) G-protein involvement in central-nervous-system muscarinic-receptor-coupled polyphosphoinositide hydrolysis. Biochem. J. 256, 995 – 999. | en_US |
dc.identifier.citedreference | Choi K. Y., Kim H. K., Lee S. Y., Moon K. H., Sim S. S., Kim J. W., Chung H. K., and Rhee S. G. ( 1990 ) Molecular cloning and expression of a complementary DNA for inositol 1,4,5-trisphosphate 3-kinase. Science 248, 64 – 66. | en_US |
dc.identifier.citedreference | Choi W. C., Gerfen C. R., Suh P. G., and Rhee S. G. ( 1989 ) Immunohistochemical localization of a brain isozyme of phospholipase C (PLC III) in astroglia in rat brain. Brain Res. 499, 193 – 197. | en_US |
dc.identifier.citedreference | Cholewinski A. J., Hanley M. R., and Wilkin G. P. ( 1988 ) A phosphoinositide-linked peptide response in astrocytes: evidence for regional heterogeneity. Neurochem. Res. 13, 389 – 394. | en_US |
dc.identifier.citedreference | Chuang D.-M. and Dillon-Carter O. ( 1988 ) Characterization of bradykinin-induced phosphoinositide turnover in neurohybrid NCB-20 cells. J. Neurochem. 51, 505 – 513. | en_US |
dc.identifier.citedreference | Cioffi C. L. and Fisher S. K. ( 1990 ) Reduction of muscarinic receptor density and of guanine-nucleotide stimulated phosphoinositide hydrolysis in human SH-SY-5Y neuroblastoma cells following long-term treatment with 12-O-tetradecanoylphorbol-13-acetate or mezerein. J. Neurochem. 54, 1725 – 1734. | en_US |
dc.identifier.citedreference | ClarÓ E., Garcia A., and Picatoste F. ( 1989 ) Carbachol and histamine stimulation of guanine-nucleotide-dependent phosphoinositide hydrolysis in rat brain cortical membranes. Biochem. J. 261, 29 – 35. | en_US |
dc.identifier.citedreference | Claustre Y., Rouquier L., and Scatton B. ( 1988a ) Pharmacological characterization of serotonin-stimulated phosphoinositide turnover in brain regions of the immature rat. J. Pharmacol. Exp. Ther. 244, 1051 – 1056. | en_US |
dc.identifier.citedreference | Claustre Y., BÉnavidÈs J., and Scatton B. ( 1988b ) 5-HT 1A receptor agonists inhibit carbachol-induced stimulation of phosphoinositide turnover in the rat hippocampus. Eur. J. Pharmacol. 149, 149 – 153. | en_US |
dc.identifier.citedreference | Cochet C. and Chambaz E. M. ( 1986 ) Catalytic properties of a purified phosphatidylinositol-4-phosphate kinase from rat brain. Biochem. J. 273, 25 – 31. | en_US |
dc.identifier.citedreference | Crawford M. L. A. and Young J. M. ( 1990a ) Ca 2+ -dependence provides evidence for differing mechanisms of GABA-induced inositol phosphate formation and GABA potentiation of inositol phosphate formation induced by noradrenaline in rat cerebral cortex. Mol. Brain Res. 8, 181 – 183. | en_US |
dc.identifier.citedreference | Crawford M. L. A. and Young J. M. ( 1990b ) Potentiation by Γ-aminobutyric acid of Α 1 -agonist-induced accumulation of inositol phosphates in slices of rat cerebral cortex. J. Neurochem. 54, 2100 – 2109. | en_US |
dc.identifier.citedreference | Crawford M. L. A., Hiley C. R., and Young J. M. ( 1990 ) Characteristics of endothelin-1 and endothelin-3 stimulation of phosphoinositide breakdown differ between regions of guinea-pig and rat brain. Naunyn–Schmiedebergs Arch. Pharmacol. 341, 268 – 271. | en_US |
dc.identifier.citedreference | Crooke S. T. and Bennett C. F. ( 1989 ) Mammalian phosphoinositide-specific phospholipase C isoenzymes. Cell Calcium 10, 309 – 323. | en_US |
dc.identifier.citedreference | Cubitt A. B., Geras-Raaka E., and Gershengorn M. C. ( 1990 ) Thyrotropin-releasing hormone receptor occupancy determines the fraction of the responsive pool of inositol lipids hydrolysed in rat pituitary tumour cells. Biochem. J. 271, 331 – 336. | en_US |
dc.identifier.citedreference | Danoff S. K., Supattapone S., and Snyder S. H. ( 1988 ) Characterization of a membrane protein from brain mediating the inhibition of inositol 1,4,5-trisphosphate receptor binding by calcium. Biochem. J. 254, 701 – 705. | en_US |
dc.identifier.citedreference | Danoff S. K., Ferris C. D., Donath C., Fischer G. A., Munemitsu S., Ullrich A., Snyder S. H., and Ross C. A. ( 1991 ) Inositol 1,4,5-trisphosphate receptors: distinct neuronal and nonneuronal forms derived by alternative splicing differ in phosphorylation. Proc. Natl. Acad. Sci. USA 88, 2951 – 2955. | en_US |
dc.identifier.citedreference | Davidson J. S., Wakefield I. K., Sohnius, U., van der Merwe P. A., and Millar R. P. ( 1990 ) A novel extracellular nucleotide receptor coupled to phosphoinositidase-C in pituitary cells. Endocrinology 126, 80 – 87. | en_US |
dc.identifier.citedreference | Day N. S., Berti-Mattera L. N., and Eichberg J. ( 1991 ) Muscarinic cholinergic receptor-mediated phosphoinositide metabolism in peripheral nerve. J. Neurochem. 56, 1905 – 1913. | en_US |
dc.identifier.citedreference | Desai M. and Conn P. J. ( 1990 ) Selective activation of phosphoinositide hydrolysis by a rigid analogue of glutamate. Neurosci. Lett. 109, 157 – 162. | en_US |
dc.identifier.citedreference | Desrues L., Tonon M. C., and Vaudry H. ( 1990 ) Thyrotropin-releasing hormone stimulates polyphosphoinositide metabolism in the frog neurointermediate lobe. J. Mol. Endocrinol. 5, 129 – 136. | en_US |
dc.identifier.citedreference | Diehl R. E., Whiting P., Potter J., Gee N., Ragan I., Linemeyer D., Schoepfer R., Bennett C., and Dixon R. A. F. ( 1990 ) Cloning and expression of bovine brain inositol monophosphatase. J. Biol. Chem. 265, 5946 – 5949. | en_US |
dc.identifier.citedreference | DoniÉ F., HÜlser E., and Reiser G. ( 1990 ) High-affinity inositol 1,3,4,5-tetrakisphosphate receptor from cerebellum: solubilization, partial purification and characterization. FEBS Lett. 268, 194 – 198. | en_US |
dc.identifier.citedreference | Downes C. P. and MacPhee C. H. ( 1990 ) myo-Inositol metabolites as cellular signals. Eur. J. Biochem. 193, 1 – 18. | en_US |
dc.identifier.citedreference | Downes C. P. and Stone M. A. ( 1986 ) Lithium-induced reduction in intracellular inositol supply in cholinergically stimulated parotid gland. Biochem. J. 234, 199 – 204. | en_US |
dc.identifier.citedreference | Drummond A. H. and Raeburn C. A. ( 1984 ) The interaction of lithium with thyrotropin releasing hormone-stimulated lipid metabolism in GH 3 pituitary tumor cells. Biochem. J. 224, 129 – 136. | en_US |
dc.identifier.citedreference | Dudek S. M. and Bear M. F. ( 1989 ) A biochemical correlate of the critical period for synaptic modification in the visual cortex. Science 246, 673 – 675. | en_US |
dc.identifier.citedreference | Dudek S. M., Bowen W. D., and Bear M. F. ( 1989 ) Postnatal changes in glutamate stimulated phosphoinositide turnover in rat neo-cortical synaptoneurosomes. Dev. Brain Res. 47, 123 – 128. | en_US |
dc.identifier.citedreference | Dyck L. E. ( 1990 ) Effects of dopamine on phosphoinositide hydrolysis in slices of rat striatum and cortex. Neurochem. Int. 17, 77 – 82. | en_US |
dc.identifier.citedreference | Eberhard D. A. and Holz R. W. ( 1988 ) Intracellular Ca 2+ activates phospholipase C. Trends Neurosci. 11, 517 – 520. | en_US |
dc.identifier.citedreference | Eberhard D. A., Cooper C. L., Low M. G., and Holz R. W. ( 1990 ) Evidence that the inositol phospholipids are necessary for exocytosis. Biochem. J. 268, 15 – 25. | en_US |
dc.identifier.citedreference | Ehrlich Y. H., Snider R. M., Kornecik E., Garfield M. G., and Lenox R. H. ( 1988 ) Modulation of neuronal signal transduction systems by extracellular ATP. J. Neurochem. 50, 295 – 301. | en_US |
dc.identifier.citedreference | , Eisenberg F. ( 1967 ) D-Myoinositol 1-phosphate as product of cyclization of glucose 6-phosphate and substrate for a specific phosphatase in rat testis. J. Biol. Chem. 242, 1375 – 1382. | en_US |
dc.identifier.citedreference | Ellis J., Huyler J. H., Kemp D. E., and Weiss S. ( 1990 ) Muscarinic receptors and second-messenger responses of neurons in primary culture. Brain Res. 511, 234 – 240. | en_US |
dc.identifier.citedreference | Emori Y., Homma Y., Sorimachi H., Kawasaki H., Nakanishi O., Suzuki K., and Takenawa T. ( 1989 ) A second type of rat phosphoinositide-specific phospholipase C containing a src-related sequence not essential for phosphoinositide-hydrolyzing activity. J. Biol. Chem. 264, 21885 – 21890. | en_US |
dc.identifier.citedreference | Endemann G., Dunn S. N., Cantley L. C. ( 1987 ) Bovine brain contains two types of phosphatidylinositol kinase. Biochemistry 26, 6845 – 6852. | en_US |
dc.identifier.citedreference | Endemann G. C., Graziani A., and Cantley L. C. ( 1991 ) A monoclonal antibody distinguishes two types of phosphatidylinositol 4-kinase. Biochem. J. 273, 63 – 66. | en_US |
dc.identifier.citedreference | Erneux C., Delvaux A., Moreau C., and Dumont J. E. ( 1986 ) Characterization of D-myo-inositol 1,4,5-trisphosphate phosphatase in rat brain. Biochem. Biophys. Res. Commun. 134, 351 – 358. | en_US |
dc.identifier.citedreference | Eva C., Gamalero S. R., Genazzani E., and Costa E. ( 1990 ) Molecular mechanisms of homologous desensitization and internalization of muscarinic receptors in primary cultures of neonatal corticostriatal neurons. J. Pharmacol. Exp. Ther. 253, 257 – 265. | en_US |
dc.identifier.citedreference | Fain J. N., Wallace M. A., and Wojcikiewicz R. J. H. ( 1988 ) Evidence for involvement of guanine nucleotide-binding regulatory proteins in the activation of phospholipases by hormones. FASEB J. 2, 2569 – 2574. | en_US |
dc.identifier.citedreference | Ferguson M. A. J. and Williams A. F. ( 1988 ) Cell-surface anchoring of proteins via glycosylphosphatidylinositol structures. Annu. Rev. Biochem. 57, 285 – 320. | en_US |
dc.identifier.citedreference | Ferris C. D., Huganir R. L., Supattapone S., and Snyder S. H. ( 1989 ) Purified inositol 1,4,5-trisphosphate receptor mediates calcium flux in reconstituted lipid vesicles. Nature 342, 87 – 89. | en_US |
dc.identifier.citedreference | Ferris C. D., Huganir R. L., and Snyder S. H. ( 1990 ) Calcium flux mediated by purified inositol 1,4,5-trisphosphate receptor in reconstituted lipid vesicles is allosterically regulated by adenine nucleotides. Proc. Natl. Acad. Sci. USA 87, 2147 – 2151. | en_US |
dc.identifier.citedreference | Fisher S. K. and Agranoff B. W. ( 1987 ) Receptor activation and inositol lipid hydrolysis in neural tissues. J. Neurochem. 48, 999 – 1016. | en_US |
dc.identifier.citedreference | Fisher S. K. and Heacock A. M. ( 1988 ) A putative M 3 muscarinic cholinergic receptor of high molecular weight couples to phosphoinositide hydrolysis in human SK-N-SH neuroblastoma cells. J. Neurochem. 50, 984 – 987. | en_US |
dc.identifier.citedreference | Fisher S. K. and Landon R. E. ( 1991 ) Identification of multiple phosphoinositide-linked receptors on human SK-N-MC neuroepithelioma cells. J. Neurochem. 57, 1599 – 1608. | en_US |
dc.identifier.citedreference | Fisher S. K., Domask L. M., and Roland R. M. ( 1989 ) Muscarinic receptor regulation of cytoplasmic Ca 2+ concentrations in human SK-N-SH neuroblastoma cells: Ca 2+ requirements for phospholipase C activation. Mol. Pharmacol. 35, 195 – 204. | en_US |
dc.identifier.citedreference | Fisher S. K., Heacock A. M., Seguin E. B., and Agranoff B. W. ( 1990 ) Polyphosphoinositides are the major source of inositol phosphates in carbamoylcholine-stimulated SK-N-SH neuroblastoma cells. Mol. Pharmacol. 38, 54 – 63. | en_US |
dc.identifier.citedreference | Forray C. and El-Fakahany E. E. ( 1990 ) On the involvement of multiple muscarinic receptor subtypes in the activation of phosphoinositide metabolism in rat cerebral cortex. Mol. Pharmacol. 37, 893 – 902. | en_US |
dc.identifier.citedreference | Fouchier F., Baltz T., and Rougon G. ( 1990 ) Identification of glycosylphosphatidylinositol-specific phospholipases C in mouse brain membranes. Biochem. J. 269, 321 – 327. | en_US |
dc.identifier.citedreference | Furuichi T., Yoshikawa S., Miyawaki A., Wada K., Maeda N., and Mikoshiba K. ( 1989 ) Primary structure and functional expression of the inositol 1,4,5-trisphosphate-binding protein P 400. Nature 342, 32 – 38. | en_US |
dc.identifier.citedreference | Gammon C. M., Allen A. C., and Morell P. ( 1989 ) Bradykinin stimulates phosphoinositide hydrolysis and mobilization of arachidonic acid in dorsal root ganglion neurons. J. Neurochem. 53, 95 – 101. | en_US |
dc.identifier.citedreference | Gee N. S., Reid G. G., Jackson R. G., Barnaby R. J., and Ragan C. I. ( 1988a ) Purification and properties of inositol-1,4-bisphosphatase from bovine brain. Biochem. J. 253, 777 – 782. | en_US |
dc.identifier.citedreference | Gee N. S., Ragan C. I., Watling K. J., Aspley S., Jackson R. G., Reid G. G., Gani D., and Shute J. K. ( 1988b ) The purification and properties of myo-inositol monophosphatase from bovine brain. Biochem. J. 249, 883 – 889. | en_US |
dc.identifier.citedreference | Gerfen C. R., Choi W. C., Suh P. G., and Rhee S. G. ( 1988 ) Phospholipase C I and II brain isozymes: immunohistochemical localization in neuronal systems in rat brain. Proc. Natl. Acad. Sci. USA 85, 3208 – 3212. | en_US |
dc.identifier.citedreference | Godfrey P. P. and Watson S. P. ( 1988 ) Fluoride inhibits agonist-induced formation of inositol phosphates in rat cortex. Biochem. Biophys. Res. Commun. 155, 664 – 669. | en_US |
dc.identifier.citedreference | Godfrey P. P., McClue S. J., Young M. M., and Heal D. J. ( 1988 ) 5-Hydroxytryptamine-stimulated inositol phospholipid hydrolysis in the mouse cortex has pharmacological characteristics compatible with mediation via 5-HT 2 receptors but this response does not reflect altered 5-HT 2 function after 5,7-dihydroxytryptamine lesioning or repeated antidepressant treatments. J. Neurochem. 50, 730 – 738. | en_US |
dc.identifier.citedreference | Godfrey P. P., McClue S. J., White A. M., Wood A. J., and Grahame-Smith D. G. ( 1989 ) Subacute and chronic in vivo lithium treatment inhibits agonist- and sodium fluoride-stimulated inositol phosphate production in rat cortex. J. Neurochem. 52, 498 – 506. | en_US |
dc.identifier.citedreference | Goldschmidt-Clermont P. J., Machesky L. M., Baldassare J. J., and Pollard T. D. ( 1990 ) The actin-binding protein profilin binds to PIP 2 and inhibits its hydrolysis by phospholipase C. Science 247, 1575 – 1578. | en_US |
dc.identifier.citedreference | Gonzales R. A. and Crews F. T. ( 1985 ) Guanine nucleotides stimulate production of inositol trisphosphate in rat cortical membranes. Biochem. J. 232, 799 – 804. | en_US |
dc.identifier.citedreference | Gonzales R. A. and Crews F. T. ( 1988 ) Differential regulation of phosphoinositide phosphodiesterase activity in brain membranes by guanine nucleotides and calcium. J. Neurochem. 50, 1522 – 1528. | en_US |
dc.identifier.citedreference | Gonzales R. A. and Moerschbaecher J. M. ( 1989 ) A phencyclidine recognition site is associated with N-methyl-D-aspartate inhibition of carbachol-stimulated phosphoinositide hydrolysis in rat cortical slices. Mol. Pharmacol. 35, 787 – 794. | en_US |
dc.identifier.citedreference | Grandison L. ( 1990 ) Platelet activating factor induces inositol phosphate accumulation in cultures of rat and bovine anterior pituitary cells. Endocrinology 127, 1786 – 1791. | en_US |
dc.identifier.citedreference | Greene D. A. and Lattimer S. A. ( 1985 ) Altered nerve myo-inositol metabolism in experimental diabetes and its relationship to nerve function, in Inositol and Phosphoinositides: Metabolism and Biological Regulation ( Bleasdale J. E., Eichberg J., Hauser G., eds ), pp. 563 – 582. Humana Press, Clifton, New Jersey. | en_US |
dc.identifier.citedreference | Guiramand J., Sassetti I., and Recasens M. ( 1989 ) Developmental changes in the chemosensitivity of rat brain synaptoneurosomes to excitatory amino acids, estimated by inositol phosphate formation. Int. J. Dev. Neurosci. 7, 257 – 266. | en_US |
dc.identifier.citedreference | Guiramand J., Mayat E., Bartolami S., Lenoir M., Rumigny J.-F., Pujol R., and RÉcasens M. ( 1990 ) A M 3 muscarinic receptor coupled to inositol phosphate formation in the rat cochlea ? Biochem. Pharmacol. 39, 1913 – 1919. | en_US |
dc.identifier.citedreference | Gusovsky F., Yasumoto T., and Daly J. W. ( 1989 ) Maitotoxin, a potent, general activator of phosphoinositide breakdown. FEBS Lett. 243, 307 – 312. | en_US |
dc.identifier.citedreference | Hallcher L. M. and Sherman W. R. ( 1980 ) The effects of lithium ion and other agents on the activity of myo-inositol-1-phosphatase from bovine brain. J. Biol. Chem. 255, 10896 – 10901. | en_US |
dc.identifier.citedreference | Hamm H. E., Deretic D., Arendt A., Hargrave P. A., Koenig B., and Hofmann K. P. ( 1988 ) Site of G protein binding to rhodopsin mapped with synthetic peptides from the Α subunit. Science 241, 832 – 835. | en_US |
dc.identifier.citedreference | Hanft G. and Gross G. ( 1989 ) Subclassification of Α 1 -adrenoceptor recognition sites by urapidil derivatives and other selective antagonists. Br. J. Pharmacol. 97, 691 – 700. | en_US |
dc.identifier.citedreference | Hansen C. A., Johanson R. A., Williamson M. T., and Williamson J. R. ( 1987 ) Purification and characterization of two types of soluble inositol phosphate 5-phosphomonoesterases from rat brain. J. Biol. Chem. 262, 17319 – 17326. | en_US |
dc.identifier.citedreference | Hansson E., Simonsson P., and Alling C. ( 1990 ) Interactions between cyclic AMP and inositol phosphate transduction systems in astrocytes in primary culture. Neuropharmacology 29, 591 – 598. | en_US |
dc.identifier.citedreference | Harootunian A. T., Kao J. P. Y., Paranjape S., and Tsien R. Y. ( 1991 ) Generation of calcium oscillations in fibroblasts by positive feedback between calcium and IP 3. Science 251, 75 – 78. | en_US |
dc.identifier.citedreference | Harwood J. L. and Hawthorne J. N. ( 1969 ) The properties and subcellular distribution of phosphatidylinositol kinase in mammalian tissues. Biochim. Biophys. Acta 171, 75 – 88. | en_US |
dc.identifier.citedreference | Hawkins P. T., Reynolds D. J. M., Poyner D. R., and Hanley M. R. ( 1990 ) Identification of a novel inositol phosphate recognition site: specific [ 3 H]inositol hexakisphosphate binding to brain regions and cerebellar membranes. Biochem. Biophys. Res. Commun. 167, 819 – 827. | en_US |
dc.identifier.citedreference | Heacock A. M., Seguin E. B., and Agranoff B. W. ( 1990 ) Developmental and regional studies of the metabolism of inositol 1,4,5-trisphosphate in rat brain. J. Neurochem. 54, 1405 – 1411. | en_US |
dc.identifier.citedreference | Hide I., Kato T., and Yamawaki S. ( 1989 ) In vivo determination of 5-hydroxytryptamine receptor-stimulated phosphoinositide turnover in rat brain. J. Neurochem. 53, 556 – 560. | en_US |
dc.identifier.citedreference | HÖer D., Kwiatkowski A., Seib C., Rosenthal W., Schultz G., and Oberdisse E. ( 1988 ) Degradation of inositol 1,3,4,5-tetrakisphosphate by porcine brain cytosol yields inositol 1,3,4-trisphosphate and inositol 1,4,5-trisphosphate. Biochem. Biophys. Res. Commun. 154, 668 – 675. | en_US |
dc.identifier.citedreference | HÖer A., HÖer D., and Oberdisse E. ( 1990 ) Properties of a soluble inositol 1,3,4,5-tetrakisphosphate 3-phosphatase from porcine brain. Biochem. J. 270, 715 – 719. | en_US |
dc.identifier.citedreference | Hollingsworth E. B. ( 1989 ) Gastrin-releasing peptide receptor in rat brain membranes: specific binding and stimulation of phosphoinositide breakdown. Mol. Pharmacol. 35, 689 – 694. | en_US |
dc.identifier.citedreference | Homma Y., Imaki J., Nakanishi O., and Takenawa T. ( 1988 ) Isolation and characterization of two different forms of inositol phospholipid-specific phospholipase C from rat brain. J. Biol. Chem. 263, 6592 – 6598. | en_US |
dc.identifier.citedreference | Honchar M. P., Ackermann K. E., and Sherman W. R. ( 1989 ) Chronically administered lithium alters neither myo-inositol monophosphatase activity nor phosphoinositide levels in rat brain. J. Neurochem. 53, 590 – 594. | en_US |
dc.identifier.citedreference | Honchar M. P., Vogler G. P., Gish B. G., and Sherman W. R. ( 1990 ) Evidence that phosphoinositide metabolism in rat cerebral cortex stimulated by pilocarpine, physostigmine, and pargyline in vivo is not changed by chronic lithium treatment. J. Neurochem. 55, 1521 – 1525. | en_US |
dc.identifier.citedreference | Horwitz J. ( 1989 ) Muscarinic receptor stimulation increases inositolphospholipid metabolism and inhibits cyclic AMP accumulation in PC12 cells. J. Neurochem. 53, 197 – 204. | en_US |
dc.identifier.citedreference | Houamed K. M., Kuijper J. L., Gilbert T. L., Haldeman B. A., O'Hara P. J., Mulvihill E. R., Almers W., and Hagen F. S. ( 1991 ) Cloning, expression, and gene structure of a G protein-coupled glutamate receptor from rat brain. Science 252, 1318 – 1321. | en_US |
dc.identifier.citedreference | Howell S., Barnaby R. J., Rowe T., Ragan C. I., and Gee N. S. ( 1989 ) Evidence for at least four different inositol bisphosphatases in bovine brain. Eur. J. Biochem. 183, 169 – 172. | en_US |
dc.identifier.citedreference | Hynie S., Wroblewski J. T., and Costa E. ( 1989 ) Profile of phosphatidylinositol metabolism stimulated by carbachol and glutamate in primary cultures of rat cerebellar neurons. Neuropharmacology 28, 1309 – 1315. | en_US |
dc.identifier.citedreference | Imaizumi T., Osugi T., Misaki N., Uchida S., and Yoshida H. ( 1989 ) Heterologous desensitization of bradykinin-induced phosphatidylinositol response and Ca 2+ mobilization by neurotensin in NG108-15 cells. Eur. J. Pharmacol. 161, 203 – 208. | en_US |
dc.identifier.citedreference | Inhorn R. C. and Majerus P. W. ( 1987 ) Inositol polyphosphate 1-phosphatase from calf brain. J. Biol. Chem. 262, 15946 – 15952. | en_US |
dc.identifier.citedreference | Inhorn R. C. and Majerus P. W. ( 1988 ) Properties of inositol polyphosphate 1-phosphatase. J. Biol. Chem. 263, 14559 – 14565. | en_US |
dc.identifier.citedreference | Ivins K. J. and Molinoff P. B. ( 1990 ). Serotonin-2 receptors coupled to phosphoinositide hydrolysis in a clonal cell line. Mol. Pharmacol. 37, 622 – 630. | en_US |
dc.identifier.citedreference | Ivorra I., Gigg R., Irvine R. F., and Parker I. ( 1991 ) Inositol 1,3,4,6-tetrakisphosphate mobilizes calcium in Xenopus oocytes with high potency. Biochem. J. 273, 317 – 321. | en_US |
dc.identifier.citedreference | Johanson R. A., Hansen C. A., and Williamson J. R. ( 1988 ) Purification of D-myo-inositol 1,4,5-trisphosphate 3-kinase from rat brain. J. Biol. Chem. 263, 7465 – 7471. | en_US |
dc.identifier.citedreference | Jones C. R., Hiley C. R., Pelton J. T., and Mohr M. ( 1989 ) Autoradiographic visualization of the binding sites for [ 125 I]endothelin in rat and human brain. Neurosci. Lett. 97, 276 – 279. | en_US |
dc.identifier.citedreference | Jones T. H., Brown B. L., and Dobson P. R. M. ( 1989 ) Bradykinin stimulates phosphoinositide metabolism and prolactin secretion in rat anterior pituitary cells. J. Mol. Endocrinol. 2, 47 – 53. | en_US |
dc.identifier.citedreference | Jope R. S. ( 1988 ) Modulation of phosphoinositide hydrolysis by NaF and aluminum in rat cortical slices. J. Neurochem. 51, 1731 – 1736. | en_US |
dc.identifier.citedreference | Jope R. S. and Li X. ( 1989 ) Inhibition of inositol phospholipid synthesis and norepinephrine-stimulated hydrolysis in rat brain slices by excitatory amino acids. Biochem. Pharmacol. 38, 589 – 596. | en_US |
dc.identifier.citedreference | Joseph S. K. and Williamson J. R. ( 1989 ) Inositol polyphosphates and intracellular calcium release. Arch. Biochem. Biophys. 273, 1 – 15. | en_US |
dc.identifier.citedreference | Kanoh H., Yamada K., and Sakane F. ( 1990 ) Diacylglycerol kinase: a key modulator of signal transduction ? Trends Biochem. Sci. 15, 47 – 50. | en_US |
dc.identifier.citedreference | Katan M. and Parker P. J. ( 1987 ) Purification of phosphoinositide-specific phospholipase C from a particulate fraction of bovine brain. Eur. J. Biochem. 168, 413 – 418. | en_US |
dc.identifier.citedreference | Kelly E., Batty I., and Nahorski S. R. ( 1988 ) Dopamine receptor stimulation does not affect phosphoinositide hydrolysis in slices of rat striatum. J. Neurochem. 51, 918 – 924. | en_US |
dc.identifier.citedreference | Kendall D. A. and Firth J. L. ( 1990 ) Inositol phospholipid hydrolysis in human brain; adenosine inhibition of the response to histamine. Br. J. Pharmacol. 100, 37 – 40. | en_US |
dc.identifier.citedreference | Kendall D. A. and Hill S. J. ( 1988 ) Adenosine inhibition of histamine-stimulated inositol phospholipid hydrolysis in mouse cerebral cortex. J. Neurochem. 50, 497 – 502. | en_US |
dc.identifier.citedreference | Kendall D. A. and Nahorski S. R. ( 1987 ) Acute and chronic lithium influence agonist and depolarization-stimulated inositol phospholipid hydrolysis in rat cerebral cortex. J. Pharmacol. Exp. Ther. 241, 1023 – 1027. | en_US |
dc.identifier.citedreference | Kennington A. S., Hill C. R., Craig J., Bogardus C., Raz I., Ortmeyer H. K., Hansen B. C., Romero G., and Larner J. ( 1990 ) Low urinary chiro-inositol excretion in non–insulin-dependent diabetes mellitus. N. Engl. J. Med. 323, 373 – 378. | en_US |
dc.identifier.citedreference | Kim U. H., Kim J. W., and Rhee S. G. ( 1989 ) Phosphorylation of phospholipase C-gamma by cAMP-dependent protein kinase. J. Biol. Chem. 264, 20167 – 20170. | en_US |
dc.identifier.citedreference | Klenk E. and Hendricks U. W. ( 1961 ) An inositol phosphatide containing carbohydrate, isolated from human brain. Biochim. Biophys. Acta 50, 602 – 603. | en_US |
dc.identifier.citedreference | Kloog Y., Ambar I., Sokolovsky M., Kochva E., Wollberg Z., and Bdolah A. ( 1988 ) Sarafotoxin, a novel vasoconstrictor peptide: phosphoinositide hydrolysis in rat heart and brain. Science 242, 268 – 270. | en_US |
dc.identifier.citedreference | Kloog Y., Ambar I., Kochva E., Wollberg Z., Bdolah A., and Sokolovsky M. ( 1989 ) Sarafotoxin receptors mediate phosphoinositide hydrolysis in various rat brain regions. FEBS Lett. 242, 387 – 390. | en_US |
dc.identifier.citedreference | Kunysz E., Michel A. D., Whiting R. L., and Woods K. ( 1989 ) The human astrocytoma cell line 1321 N1 contains M 2 -glandular type muscarinic receptors linked to phosphoinositide turnover. Br. J. Pharmacol. 96, 271 – 278. | en_US |
dc.identifier.citedreference | Lambert D. G., Ghataorre A. S., and Nahorski S. R. ( 1989 ) Muscarinic receptor binding characteristics of a human neuroblastoma SK-N-SH and its clones SH-SY-5Y and SH-EP1. Eur. J. Pharmacol. 165, 71 – 77. | en_US |
dc.identifier.citedreference | Lee K.-Y., Ryu S. H., Suh P.-G., Choi W. C., and Rhee S. G. ( 1987 ) Phospholipase C associated with particulate fractions of bovine brain. Proc. Natl. Acad. Sci. USA 84, 5540 – 5544. | en_US |
dc.identifier.citedreference | Lee S. Y., Sim S. S., Kim J. W., Moon K. H., Kim J. H., and Rhee S. G. ( 1990 ) Purification and properties of D-myo-inositol 1,4,5-trisphosphate 3-kinase from rat brain. J. Biol. Chem. 265, 9434 – 9440. | en_US |
dc.identifier.citedreference | Lenox R. H., Hendley D., and Ellis J. ( 1988 ) Desensitization of muscarinic receptor-coupled phosphoinositide hydrolysis in rat hippocampus: comparisons with the Α 1 -adrenergic response. J. Neurochem. 50, 558 – 564. | en_US |
dc.identifier.citedreference | Lester H. A. ( 1988 ) Heterologous expression of excitability proteins: route to more specific drugs ?. Science 241, 1057 – 1063. | en_US |
dc.identifier.citedreference | Li P. P., Sibony D., and Warsh J. J. ( 1990 ) Guanosine 5′-O-thiotriphosphate and sodium fluoride activate polyphosphoinositide hydrolysis in rat cortical membranes by distinct mechanisms. J. Neurochem. 54, 1426 – 1432. | en_US |
dc.identifier.citedreference | Li X., Song L., and Jope R. S. ( 1990 ) Modulation of phosphoinositide metabolism in rat brain slices by excitatory amino acids, arachidonic acid, and GABA. Neurochem. Res. 15, 725 – 738. | en_US |
dc.identifier.citedreference | Liang M., Martin M. W., and Harden T. K. ( 1987 ) [ 3 H]-Propylbenzilylcholine mustard-labeling of muscarinic cholinergic receptors that selectively couple to phospholipase C or adenylate cyclase in two cultured cell lines. Mol. Pharmacol. 32, 443 – 449. | en_US |
dc.identifier.citedreference | Lin W.-W., Lee C. Y., and Chuang D.-M. ( 1990 ) Comparative studies of phosphoinositide hydrolysis induced by endothelin-related peptides in cultured cerebellar astrocytes, C 6 -glioma and cerebellar granule cells. Biochem. Biophys. Res. Commun. 168, 512 – 519. | en_US |
dc.identifier.citedreference | Lips D. L. and Majerus P. W. ( 1989 ) The discovery of a 3-phosphomonoesterase that hydrolyzes phosphatidylinositol 3-phosphate in NIH 3T3 cells. J. Biol. Chem. 264, 19911 – 19915. | en_US |
dc.identifier.citedreference | Lips D. L., Majerus P. W., Gorga F. R., Young A. T., and Benjamin T. L. ( 1989 ) Phosphatidylinositol 3-phosphate is present in normal and transformed fibroblasts and is resistant to hydrolysis by bovine brain phospholipase C II. J. Biol. Chem. 264, 8759 – 8763. | en_US |
dc.identifier.citedreference | Lisanti M. P., Rodriguez-Boulan E., and Saltiel A. R. ( 1990 ) Emerging functional roles for the glycosylphosphatidylinositol membrane protein anchor. J. Membr. Biol. 117, 1 – 10. | en_US |
dc.identifier.citedreference | Litosch I. ( 1987 ) Guanine nucleotide and NaF stimulation of phospholipase C activity in rat cerebral-cortical membranes. Biochem. J. 244, 35 – 40. | en_US |
dc.identifier.citedreference | Litosch I. ( 1989 ) Guanine nucleotides mediate stimulatory and inhibitory effects on cerebral-cortical membrane phospholipase C activity. Biochem. J. 261, 245 – 251. | en_US |
dc.identifier.citedreference | Lo W. W. Y. and Hughes J. ( 1988 ) Differential regulation of chotecystokinin- and muscarinic-receptor-mediated phosphoinositide turnover in Flow 9000 cells. Biochem. J. 251, 625 – 630. | en_US |
dc.identifier.citedreference | Low M. G. ( 1989 ) Glycosyl-phosphatidylinositol: a versatile anchor for cell surface proteins. FASEB J. 3, 1600 – 1608. | en_US |
dc.identifier.citedreference | Low M. G. and Kincade P. W. ( 1985 ) Phosphatidylinositol is the membrane-anchoring domain of the Thy-1 glycoprotein. Nature 318, 62 – 64. | en_US |
dc.identifier.citedreference | MacCumber M. W., Ross C. A., and Snyder S. H. ( 1990 ) Endothelin in brain: receptors, mitogenesis, and biosynthesis in glial cells. Proc. Natl. Acad. Sci. USA 87, 2359 – 2363. | en_US |
dc.identifier.citedreference | Maeda N., Niinobe M., Inoue Y., and Mikoshiba K. ( 1989 ) Developmental expression and intracellular location of P 400 protein characteristic of Purkinje cells in the mouse cerebellum. Dev. Biol. 133, 67 – 76. | en_US |
dc.identifier.citedreference | Maeda N., Niinobe M., and Mikoshiba K. ( 1990 ) A cerebellar Purkinje cell marker P 400 protein is an inositol 1,4,5-trisphosphate (InsP 3 ) receptor protein. Purification and characterization of InsP 3 receptor complex. EMBO J. 9, 61 – 67. | en_US |
dc.identifier.citedreference | Maeda N., Kawasaki T., Nakade S., Yokota N., Taguchi T., Kasai M., and Mikoshiba K. ( 1991 ) Structural and functional characterization of inositol 1,4,5-trisphosphate receptor channel from mouse cerebellum. J. Biol. Chem. 266, 1109 – 1116. | en_US |
dc.identifier.citedreference | Mahan L. C., Burch R. M., Monsma, F. J., and Sibley D. R. ( 1990 ) Expression of striatal D 1 dopamine receptors coupled to inositol phosphate production and Ca 2+ mobilization in Xenopus oocytes. Proc. Natl. Acad. Sci. USA 87, 2196 – 2200. | en_US |
dc.identifier.citedreference | Mailleux P., Takazawa K., Erneux C., and Vanderhaeghen J.-J. ( 1991 ) Inositol 1,4,5-trisphosphate 3-kinase mRNA: high levels in the rat hippocampal CA1 pyramidal and dentate gyrus granule cells and in cerebellar Purkinje cells. J. Neurochem. 56, 345 – 347. | en_US |
dc.identifier.citedreference | Majerus P. W., Ross T. S., Cunningham T. W., Caldwell K. K., Jefferson A. B., and Bansal V. S. ( 1990 ) Recent insights in phosphatidylinositol signaling. Cell 63, 459 – 465. | en_US |
dc.identifier.citedreference | Malhotra R. K., Bhave S. V., Wakade T. D., Bhave A. S., and Wakade A. R. ( 1990 ) Effects of neurotransmitters and peptides on phospholipid hydrolysis in sympathetic and sensory neurons. FASEB J. 4, 2492 – 2498. | en_US |
dc.identifier.citedreference | Mallet J., Huchet M., Pougeois R., and Changeux J.-P. ( 1976 ) Anatomical, physiological and biochemical studies on the cerebellum from mutant mice. III. Protein differences associated with the weaver, staggerer and nervous mutations. Brain Res. 103, 291 – 312. | en_US |
dc.identifier.citedreference | Manzoni O., Fagni L., Pin J.-P., Rassendren F., Poulat F., Sladeczek F., and Bockaert J. ( 1990 ) (trans)-1-Amino-cyclopentyl-1,3-dicarboxylate stimulates quisqualate phosphoinositide-coupled receptors but not ionotropic glutamate receptors in striatal neurons and Xenopus oocytes. Mol. Pharmacol. 38, 1 – 6. | en_US |
dc.identifier.citedreference | Margolis R. K., Goossen B., and Margolis R. U. ( 1988 ) Phosphatidylinositol-anchored glycoproteins of PC12 pheochromocytoma cells and brain. Biochemistry 27, 3454 – 3458. | en_US |
dc.identifier.citedreference | Masu M., Tanabe Y., Tsuchida K., Shigemoto R., and Nakanishi S. ( 1991 ) Sequence and expression of a metabotropic glutamate receptor. Nature 349, 760 – 765. | en_US |
dc.identifier.citedreference | Mau S. E., Larsen P. J., Mikkelsen J. A., and SÆ;rmark T. ( 1990 ) Substance P and related tachykinins induce receptor-mediated hydrolysis of polyphosphoinositides in the rat anterior pituitary. Mol. Cell. Endocrinol. 69, 69 – 78. | en_US |
dc.identifier.citedreference | McAtee P. and Dawson G. ( 1990 ) Phospholipase C activity in NCB-20 cells is inhibited by protein kinase A-mediated phosphorylation of low molecular mass GTP-binding proteins. J. Biol. Chem. 265, 6788 – 6793. | en_US |
dc.identifier.citedreference | Meek J. L., Rice T. J., and Anton E. ( 1988 ) Rapid purification of inositol monophosphate phosphatase from beef brain. Biochem. Biophys. Res. Commun. 156, 143 – 148. | en_US |
dc.identifier.citedreference | Meyer T., Holowka D., and Stryer L. ( 1988 ) Highly cooperative opening of calcium channels by inositol 1,4,5-trisphosphate. Science 240, 653 – 655. | en_US |
dc.identifier.citedreference | Michel M. C., Hanft G., and Gross G. ( 1990 ) Α 1B - but not Α 1A -adrenoceptors mediate inositol phosphate generation. Naunyn–Schmiedebergs Arch. Pharmacol. 341, 385 – 387. | en_US |
dc.identifier.citedreference | Mignery G. A., SÜdhof T. C., Takei K., and De Camilli P. ( 1989 ) Putative receptor for inositol 1,4,5-trisphosphate similar to ryanodine receptor. Nature 342, 192 – 195. | en_US |
dc.identifier.citedreference | Mignery G. A., Newton C. L., Archer B. T., and SÜdhof T. C. ( 1990 ) Structure and expression of the rat inositol 1,4,5-trisphosphate receptor. J. Biol. Chem. 265, 12679 – 12685. | en_US |
dc.identifier.citedreference | Minneman K. P. ( 1988 ) Α 1 -Adrenergic receptor subtypes, inositol phosphates, and sources of cell Ca 2+. Pharmacol. Rev. 40, 87 – 119. | en_US |
dc.identifier.citedreference | Misawa H., Ueda H., and Satoh M. ( 1990 ) Opioid agonist inhibits phospholipase C, possibly via an inhibition of G-protein activity. Neurosci. Lett. 112, 324 – 327. | en_US |
dc.identifier.citedreference | Moratalla R., Vallejo M., and Lightman S. L. ( 1988 ) Vasopressin stimulates inositol phospholipid metabolism in rat medulla oblongata in vivo. Brain Res. 450, 398 – 402. | en_US |
dc.identifier.citedreference | Morgan S. J., Smith A. D., and Parker P. J. ( 1990 ) Purification and characterization of bovine brain type I phosphatidylinositol kinase. Eur. J. Biochem. 191, 761 – 767. | en_US |
dc.identifier.citedreference | Moritz A., De Graan P. N. E., Ekhart P. F., Gispen W. H., and Wirtz K. W. A. ( 1990 ) Purification of a phosphatidylinositol 4-phosphate kinase from bovine brain membranes. J. Neurochem. 54, 351 – 354. | en_US |
dc.identifier.citedreference | Moroi-Fetters S. E., Neff N. H., and Hadjiconstantinou M. ( 1988 ) Muscarinic receptor-mediated phosphoinositide hydrolysis in the rat retina. J. Pharmacol. Exp. Ther. 246, 553 – 557. | en_US |
dc.identifier.citedreference | Morrisett R. A., Chow C. C., Sakaguchi T., Shin C., and McNamara J. O. ( 1990 ) Inhibition of muscarinic-coupled phosphoinositide hydrolysis by N-methyl-D-aspartate is dependent on depolarization via channel activation. J. Neurochem. 54, 1517 – 1525. | en_US |
dc.identifier.citedreference | Moyer J. D., Reizes O., Ahir S., Jiang C., Malinowski N., and Baker D. C. ( 1988 ) Substrate properties of analogs of myo-inositol. Mol. Pharmacol. 33, 683 – 689. | en_US |
dc.identifier.citedreference | Murphy S. and Welk G. ( 1990 ) Hydrolysis of polyphosphoinositides in astrocytes by platelet-activating factor. Eur. J. Pharmacol. 188, 399 – 401. | en_US |
dc.identifier.citedreference | Nahorski S. R. and Potter B. V. L. ( 1989 ) Molecular recognition of inositol polyphosphates by intracellular receptors and metabolic enzymes. Trends Pharmacol. Sci. 10, 139 – 144. | en_US |
dc.identifier.citedreference | Nakahata N. and Harden T. K. ( 1987 ) Regulation of inositol trisphosphate accumulation by muscarinic cholinergic and H 1 -histamine receptors on human astrocytoma cells. Biochem. J. 241, 337 – 344. | en_US |
dc.identifier.citedreference | Nakahata N., Matsuoka I., Ono T., and Nakanishi H. ( 1989 ) Thromboxane A 2 activates phospholipase C in astrocytoma cells via pertussis toxin-insensitive G-protein. Eur. J. Pharmacol. 162, 407 – 417. | en_US |
dc.identifier.citedreference | Nakahata N., Abe M. T., Matsuoka I., and Nakanishi H. ( 1990 ) Mastoparan inhibits phosphoinositide hydrolysis via pertussis toxin-insensitive G-protein in human astrocytoma cells. FEBS Lett. 260, 91 – 94. | en_US |
dc.identifier.citedreference | Negishi M., Ito S., and Hayaishi O. ( 1989 ) Prostaglandin E receptors in bovine adrenal medulla are coupled to adenylate cyclase via G i and to phosphoinositide metabolism in a pertussis toxin-insensitive manner. J. Biol. Chem. 264, 3916 – 3923. | en_US |
dc.identifier.citedreference | Nicoletti F. and Canonico P. L. ( 1989 ) Glycine potentiates the stimulation of inositol phospholipid hydrolysis by excitatory amino acids in primary cultures of cerebellar neurons. J. Neurochem. 53, 724 – 727. | en_US |
dc.identifier.citedreference | Nicoletti F., Wroblewski J. T., Alho H., Eva C., Fadda E., and Costa E. ( 1987 ) Lesions of putative glutamatergic pathways potentiate the increase of inositol phospholipid hydrolysis elicited by excitatory amino acids. Brain Res. 436, 103 – 112. | en_US |
dc.identifier.citedreference | Nicoletti F., Wroblewski J. T., Fadda E., and Costa E. ( 1988 ) Pertussis toxin inhibits signal transduction at a specific metabolotropic glutamate receptor in primary cultures of cerebellar granule cells. Neuropharmacology 27, 551 – 556. | en_US |
dc.identifier.citedreference | Nicoletti F., Bruno V., Cavallaro S., Copani A., Sortino M. A., and Canonico P. L. ( 1990 ) Specific binding sites for inositolhexakisphosphate in brain and anterior pituitary. Mol. Pharmacol. 37, 689 – 693. | en_US |
dc.identifier.citedreference | Nishizuka Y. ( 1988 ) The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature 334, 661 – 665. | en_US |
dc.identifier.citedreference | Noble E. P., Sincini E., Bergmann J., and ten Bruggencate G. ( 1989 ) Excitatory amino acids inhibit stimulated phosphoinositide hydrolysis in the rat prefrontal cortex. Life Sci. 44, 19 – 26. | en_US |
dc.identifier.citedreference | Nunn D. L., Potter B. V. L., and Taylor C. W. ( 1990 ) Molecular target sizes of inositol 1,4,5-trisphosphate receptors in liver and cerebellum. Biochem. J. 265, 393 – 398. | en_US |
dc.identifier.citedreference | Oakes S. G., Iaizzo P. A., Richelson E., and Powis G. ( 1988 ) Histamine-induced intracellular free Ca ++, inositol phosphates and electrical changes in murine N1E-115 neuroblastoma cells. J. Pharmacol. Exp. Ther. 247, 114 – 121. | en_US |
dc.identifier.citedreference | Orellana S., Solski P. A., and Brown J. H. ( 1987 ) Guanosine 5′-O-(thiotriphosphate)-dependent inositol triphosphate formation in membranes is inhibited by phorbol ester and protein kinase C. J. Biol. Chem. 262, 1638 – 1643. | en_US |
dc.identifier.citedreference | Osborne N. N. ( 1990 ) Stimulatory and inhibitory actions of excitatory amino acids on inositol phospholipid metabolism in rabbit retina. Evidence for a specific quisqualate receptor subtype associated with neurones. Exp. Eye Res. 50, 397 – 405. | en_US |
dc.identifier.citedreference | Osborne N. N. and Ghazi H. ( 1989 ) The effect of substance P and other tachykinins on inositol phospholipid hydrolysis in rabbit retina, superior colliculus and retinal cultures. Vision Res. 29, 757 – 764. | en_US |
dc.identifier.citedreference | Palmer E., Monaghan D. T., and Cotman C. W. ( 1989 ) trans-ACPD, a selective agonist of the phosphoinositide-coupled excitatory amino acid receptor. Eur. J. Pharmacol. 166, 585 – 587. | en_US |
dc.identifier.citedreference | Patel J., Moore W. C., Thompson C., Keith R. A., and Salama A. I. ( 1990 ) Characterization of the quisqualate receptor linked to phosphoinositide hydrolysis in neurocortical cultures. J. Neurochem. 54, 1461 – 1466. | en_US |
dc.identifier.citedreference | Pearce B., Morrow C., and Murphy S. ( 1988 ) Characteristics of phorbol ester- and agonist-induced down-regulation of astrocyte receptors coupled to inositol phospholipid metabolism. J. Neurochem. 50, 936 – 944. | en_US |
dc.identifier.citedreference | Pearce B., Murphy S., Jeremy J., Morrow C., and Dandona P. ( 1989 ) ATP-evoked Ca 2+ mobilisation and prostanoid release from astrocytes: P 2 -purinergic receptors linked to phosphoinositide hydrolysis. J. Neurochem. 52, 971 – 977. | en_US |
dc.identifier.citedreference | Pearce B., Morrow C., and Murphy S. ( 1990 ) Further characterisation of excitatory amino acid receptors coupled to phosphoinositide metabolism in astrocytes. Neurosci. Lett. 113, 298 – 303. | en_US |
dc.identifier.citedreference | Periyasamy S. and Hoss W. ( 1990 ) Kappa opioid receptors stimulate phosphoinositide turnover in rat brain. Life Sci. 47, 219 – 225. | en_US |
dc.identifier.citedreference | Perney T. M. and Miller R. J. ( 1989 ) Two different G-proteins mediate neuropeptide Y and bradykinin-stimulated phospholipid breakdown in cultured rat sensory neurons. J. Biol. Chem. 264, 7317 – 7327. | en_US |
dc.identifier.citedreference | Pfeilschifter J. ( 1990 ) Comparison of extracellular ATP and UTP signalling in rat renal mesangial cells. Biochem. J. 272, 469 – 472. | en_US |
dc.identifier.citedreference | Pierce P. A. and Peroutka S. J. ( 1988 ) Antagonism of 5-hydroxytryptamine 2 receptor-mediated phosphatidylinositol turnover by d-lysergic acid diethylamide. J. Pharmacol. Exp. Ther. 247, 918 – 925. | en_US |
dc.identifier.citedreference | Poyner D. R., Hawkins P. T., Benton H. P., and Hanley M. R. ( 1990 ) Changes in inositol lipids and phosphates after stimulation of the MAS-transfected NG 115-401L-C3 cell line by mitogenic and non-mitogenic stimuli. Biochem. J. 271, 605 – 611. | en_US |
dc.identifier.citedreference | Prasad V. N. H. and Moody T. W. ( 1989 ) Bombesin-like peptides stimulate phosphatidylinositol turnover in rat brain slices. Peptides 9, 1345 – 1349. | en_US |
dc.identifier.citedreference | Ragan C. I., Watling K. J., Gee N. S., Aspley S., Jackson R. G., Reid G. G., Baker R., Billington D. C., Barnaby R. J., and Leeson P. D. ( 1988 ) The dephosphorylation of inositol 1,4-bisphosphate to inositol in liver and brain involves two distinct Li + -sensitive enzymes and proceeds via inositol 4-phosphate. Biochem. J. 249, 143 – 148. | en_US |
dc.identifier.citedreference | Raiteri M., Marchi M., and Paudice P. ( 1987 ) Vasoactive intestinal polypeptide (VIP) potentiates the muscarinic stimulation of phosphoinositide turnover in rat cerebral cortex. Eur. J. Pharmacol. 133, 127 – 128. | en_US |
dc.identifier.citedreference | Rebecchi M. J. and Rosen O. M. ( 1987 ) Purification of a phosphoinositide-specific phospholipase C from bovine brain. J. Biol. Chem. 262, 12526 – 12532. | en_US |
dc.identifier.citedreference | Rhee S. G., Suh P.-G., Ryu S.-H., and Lee S. Y. ( 1989 ) Studies of inositol phospholipid-specific phospholipase C. Science 244, 546 – 550. | en_US |
dc.identifier.citedreference | Robertson P. L., Bruno G. R., and Datta S. C. ( 1990 ) Glutamate-stimulated, guanine nucleotide-mediated phosphoinositide turnover in astrocytes is inhibited by cyclic AMP. J. Neurochem. 55, 1727 – 1733. | en_US |
dc.identifier.citedreference | Ross C. A., Meldolesi J., Milner T. A., Satoh T., Supattapone S., and Snyder S. H. ( 1989 ) Inositol 1,4,5-trisphosphate receptor localized to endoplasmic reticulum in cerebellar Purkinje neurons. Nature 339, 468 – 470. | en_US |
dc.identifier.citedreference | Rubinstein J. E. and Hitzemann R. J. ( 1990 ) Further evidence against the coupling of dopamine receptors to phosphoinositide hydrolysis in rat striatum. Biochem. Pharmacol. 39, 1965 – 1970. | en_US |
dc.identifier.citedreference | Ryu S. H., Cho K. S., Lee K. Y., Suh P.-G., and Rhee S. G. ( 1986 ) Two forms of phosphatidylinositol-specific phospholipase C from bovine brain. Biochem. Biophys. Res. Commun. 141, 137 – 144. | en_US |
dc.identifier.citedreference | Ryu S. H., Cho K. S., Lee K.-Y., Suh P.-G., and Rhee S. G. ( 1987a ) Purification and characterization of two immunologically distinct phosphoinositide-specific phospholipase C from bovine brain. J. Biol. Chem. 262, 12511 – 12518. | en_US |
dc.identifier.citedreference | Ryu S. H., Suh P.-G., Cho K. S., Lee K.-Y., and Rhee S. G. ( 1987b ) Bovine brain cytosol contains three immunologically distinct forms of inositolphospholipid-specific phospholipase C. Proc. Natl. Acad. Sci. USA 84, 6649 – 6653. | en_US |
dc.identifier.citedreference | Saltiel A. R., Fox J. A., Sherline P., Sahyoun N., and Cuatrecasas P. ( 1987 ) Purification of phosphatidylinositol kinase from bovine brain myelin. Biochem. J. 241, 759 – 763. | en_US |
dc.identifier.citedreference | Sanders-Bush E., Burris K. D., and Knoth K. ( 1988 ) Lysergic acid diethylamide and 2,5-dimethoxy-4-methylamphetamine are partial agonists at serotonin receptors linked to phosphoinositide hydrolysis. J. Pharmacol. Exp. Ther. 246, 924 – 928. | en_US |
dc.identifier.citedreference | Sasakawa N., Nakaki T., Yamamoto S., and Kato R. ( 1989 ) Stimulation by ATP of inositol trisphosphate accumulation and calcium mobilization in cultured adrenal chromaffin cells. J. Neurochem. 52, 441 – 447. | en_US |
dc.identifier.citedreference | Sasakawa N., Nakaki T., and Kato R. ( 1990 ) Stimulus-responsive and rapid formation of inositol pentakisphosphate in cultured adrenal chromaffin cells. J. Biol. Chem. 265, 17700 – 17705. | en_US |
dc.identifier.citedreference | Satoh T., Ross C. A., Villa A., Supattapone S., Pozzan T., Snyder S. H., and Meldolesi J. ( 1990 ) The inositol 1,4,5-trisphosphate receptor in cerebellar Purkinje cells: quantitative immunogold labeling reveals concentration in an ER subcompartment. J. Cell Biol. 111, 615 – 624. | en_US |
dc.identifier.citedreference | Schoepp D. D., Johnson B. G., Smith E. C. R., and McQuaid L. A. ( 1990a ) Stereoselectivity and mode of inhibition of phosphoinositide-coupled excitatory amino acid receptors by 2-amino-3-phosphonopropionic acid. Mol. Pharmacol. 38, 222 – 228. | en_US |
dc.identifier.citedreference | Schoepp D., Bockaert J., and Sladeczek F. ( 1990b ) Pharmacological and functional characteristics of metabotropic excitatory amino acid receptors. Trends Pharmacol. Sci. 11, 508 – 515. | en_US |
dc.identifier.citedreference | Seren M. S., Aldinio C., Zanoni R., Leon A., and Nicoletti F. ( 1989 ) Stimulation of inositol phospholipid hydrolysis by excitatory amino acids is enhanced in brain slices from vulnerable regions after transient global ischemia. J. Neurochem. 53, 1700 – 1705. | en_US |
dc.identifier.citedreference | Serra M., Mei L., Roeske W. R., Lui G. K., Watson M., and Yamamura H. I. ( 1988 ) The intact human neuroblastoma cell (SH-SY5Y) exhibits high-affinity [ 3 H]pirenzepine binding associated with hydrolysis of phosphatidylinositols. J. Neurochem. 50, 1513 – 1521. | en_US |
dc.identifier.citedreference | Serunian L. A., Haber M. T., Fukui T., Kim J. W., Rhee S. G., Lowenstein J. M., and Cantley L. C. ( 1989 ) Polyphosphoinositides produced by phosphatidylinositol 3-kinase are poor substrates for phospholipases C from rat liver and bovine brain. J. Biol. Chem. 264, 17809 – 17815. | en_US |
dc.identifier.citedreference | Sharif N. A., Hunter J. C., Hill R. G., and Hughes J. ( 1988 ) Bradykinin-induced accumulation of [ 3 H]inositol-1-phosphate in human embryonic pituitary tumour cells by activation of a B 2 receptor. Neurosci. Lett. 86, 279 – 283. | en_US |
dc.identifier.citedreference | Sharif N. A., To Z., and Whiting R. L. ( 1989 ) First pharmacological characterization of TRH receptors linked to phosphoinositide hydrolysis in GH3 pituitary cells using agonist specificity of eight TRH analogs. Biochem. Biophys. Res. Commun. 161, 1306 – 1311. | en_US |
dc.identifier.citedreference | Shears S. B. ( 1989 ) Metabolism of the inositol phosphates produced upon receptor activation. Biochem. J. 260, 313 – 324. | en_US |
dc.identifier.citedreference | Shewey L. M. and Dorsa D. M. ( 1988 ) V 1 -type vasopressin receptors in rat brain septum: binding characteristics and effects on inositol phospholipid metabolism. J. Neurosci. 8, 1671 – 1677. | en_US |
dc.identifier.citedreference | Sim S. S., Kim J. W., and Rhee S. G. ( 1990 ) Regulation of D-myo-inositol 1,4,5-trisphosphate 3-kinase by cAMP-dependent protein kinase and protein kinase C. J. Biol. Chem. 265, 10367 – 10372. | en_US |
dc.identifier.citedreference | Smith C. D. and Chang K.-J. ( 1989 ) Regulation of brain phosphatidylinositol-4-phosphate kinase by GTP analogues. J. Biol. Chem. 264, 3206 – 3210. | en_US |
dc.identifier.citedreference | Smith R. J., Sam L. M., Justen J. M., Bundy G. L., Bala G. A., and Bleasdale J. E. ( 1990 ) Receptor-coupled signal transduction in human polymorphonuclear neutrophils: effects of a novel inhibitor of phospholipase C-dependent processes on cell responsiveness. J. Pharmacol. Exp. Ther. 253, 688 – 697. | en_US |
dc.identifier.citedreference | Smrcka A. V., Hepler J. R., Brown K. O., and Sternweis P. C. ( 1991 ) Regulation of polyphosphoinositide-specific phospholipase C activity by purified G q. Science 251, 804 – 807. | en_US |
dc.identifier.citedreference | Snyder S. H. and Supattapone S. ( 1989 ) Isolation and functional characterization of an inositol trisphosphate receptor from brain. Cell Calcium 10, 337 – 342. | en_US |
dc.identifier.citedreference | Sortino M. A., Evans W. S., Speciale C., Thorner M. O., Scapagnini U., MacLeod R. M., and Canonico P. L. ( 1988 ) Gonadotropin-releasing hormone-stimulated phosphoinositide hydrolysis in the anterior pituitary. Neuroendocrinology 48, 544 – 550. | en_US |
dc.identifier.citedreference | Sortino M. A., Nicoletti F., and Canonico P. L. ( 1990 ) Inositol hexakisphosphate stimulates 45 Ca 2+ uptake in anterior pituitary cells in culture. Eur. J. Pharmacol. 189, 115 – 118. | en_US |
dc.identifier.citedreference | SpÄt A., Bradford P. G., McKinney J. S., Rubin R. P., and Putney, J. W. ( 1986 ) A saturable receptor for 32 P-inositol-1,4,5-trisphosphate in hepatocytes and neutrophils. Nature 319, 514 – 516. | en_US |
dc.identifier.citedreference | Stanley A. F., Hawkins P. T., and Hanley M. R. ( 1990 ) Inositol hexakisphosphate biosynthesis in mammalian brain: identification of a novel inositol pentakisphosphate kinase. Biochem. Soc. Trans. 18, 460 – 461. | en_US |
dc.identifier.citedreference | Stephens L. R., Hawkins P. T., Barker C. J., and Downes C. P. ( 1988 ) Synthesis of myo-inositol 1,3,4,5,6-pentakisphosphate from inositol phosphates generated by receptor activation. Biochem. J. 253, 721 – 733. | en_US |
dc.identifier.citedreference | Stephens L., Hawkins P. T., and Downes C. P. ( 1989 ) Metabolic and structural evidence for the existence of a third species of polyphosphoinositide in cells: D-phosphatidyl-myo-inositol 3-phosphate. Biochem. J. 259, 267 – 276. | en_US |
dc.identifier.citedreference | Strosznajder J. and Strosznajder R. P. ( 1989 ) Stimulation of phosphoinositide degradation and phosphatidylinositol-4-phosphate phosphorylation by GTP exclusively in plasma membrane of rat brain. Neurochem. Res. 14, 717 – 723. | en_US |
dc.identifier.citedreference | Supattapone S., Worley P. F., Baraban J. M., and Snyder S. H. ( 1988 ) Solubilization, purification, and characterization of an inositol trisphosphate receptor. J. Biol. Chem. 263, 1530 – 1534. | en_US |
dc.identifier.citedreference | Sylvia V., Curtin G., Norman J., Stec J., and Busbee D. ( 1988 ) Activation of a low specific activity form of DNA polymerase Α by inositol-1,4-bisphosphate. Cell 54, 651 – 658. | en_US |
dc.identifier.citedreference | Takashima A. and Kenimer J. G. ( 1989 ) Muscarinic-stimulated norepinephrine release and phosphoinositide hydrolysis in PC12 cells are independent events. J. Biol. Chem. 264, 10654 – 10659. | en_US |
dc.identifier.citedreference | Takazawa K., Passareiro H., Dumont J. E., and Erneux C. ( 1988 ) Ca 2+ /calmodulin-sensitive inositol 1,4,5-trisphosphate 3-kinase in rat and bovine brain tissues. Biochem. Biophys. Res. Commun. 153, 632 – 641. | en_US |
dc.identifier.citedreference | Takazawa K., Lemos M., Delvaux A., Lejeune C., Dumont J. E., and Erneux C. ( 1990a ) Rat brain inositol 1,4,5-trisphosphate 3-kinase. Biochem. J. 268, 213 – 217. | en_US |
dc.identifier.citedreference | Takazawa K., Vandekerckhove J., Dumont J. E., and Erneux C. ( 1990b ) Cloning and expression in Escherichia coli of a rat brain cDNA encoding a Ca 2+ /calmodulin-sensitive inositol 1,4,5-trisphosphate 3-kinase. Biochem. J. 272, 107 – 112. | en_US |
dc.identifier.citedreference | Taylor S. J., Chae H. Z., Rhee S. G., and Exton J. H. ( 1991 ) Activation of the Β 1 isozyme of phospholipase C by Α subunits of the G q class of G protein. Nature 350, 516 – 518. | en_US |
dc.identifier.citedreference | Thompson A. K. and Fisher S. K. ( 1990 ) Relationship between agonist-induced muscarinic receptor loss and desensitization of stimulated phosphoinositide turnover in two neuroblastomas: methodological considerations. J. Pharmacol. Exp. Ther. 252, 744 – 752. | en_US |
dc.identifier.citedreference | Thompson A. K. and Fisher S. K. ( 1991 ) Preferential coupling of cell surface muscarinic receptors to phosphoinositide hydrolysis in human neuroblastoma cells. J. Biol. Chem. 266, 5004 – 5010. | en_US |
dc.identifier.citedreference | Thompson A. K., Mostafapour S. P., Denlinger L. C., Bleasdale J. E., and Fisher S. K. ( 1991 ) The aminosteroid U-73122 inhibits muscarinic receptor sequestration and phosphoinositide hydrolysis in SK-N-SH neuroblastoma cells: a role for G p in receptor compartmentation. J. Biol. Chem. (in press). | en_US |
dc.identifier.citedreference | Torrens Y., Daguet De Montety M. C., El Etr M., Beaujouan J. C., and Glowinski J. ( 1989 ) Tachykinin receptors of the NK1 type (substance P) coupled positively to phospholipase C on cortical astrocytes from the newborn mouse in primary culture. J. Neurochem. 52, 1913 – 1918. | en_US |
dc.identifier.citedreference | Undie A. S. and Friedman E. ( 1990 ) Stimulation of a dopamine D 1 receptor enhances inositol phosphate formation in rat brain. J. Pharmacol. Exp. Ther. 253, 987 – 992. | en_US |
dc.identifier.citedreference | Vadnal R. E. and Parthasarathy R. ( 1989 ) The identification of a novel inositol lipid, phosphatidylinositol trisphosphate (PIP 3 ), in rat cerebrum using in vivo techniques. Biochem. Biophys. Res. Commun. 163, 995 – 1001. | en_US |
dc.identifier.citedreference | Vallejo M., Jackson T., Lightman S., and Hanley M. R. ( 1987 ) Occurrence and extracellular actions of inositol pentakis- and hexakisphosphate in mammalian brain. Nature 330, 656 – 658. | en_US |
dc.identifier.citedreference | Van Calker D., Takahata K., and Heumann R. ( 1989 ) Nerve growth factor potentiates the hormone-stimulated intracellular accumulation of inositol phosphates and Ca 2+ in rat PC12 pheochromocytoma cells: comparison with the effect of epidermal growth factor. J. Neurochem. 52, 38 – 45. | en_US |
dc.identifier.citedreference | Van der Merwe P. A., Wakefield I. K., Fine J., Millar R. P., and Davidson J. S. ( 1989 ) Extracellular adenosine triphosphate activates phospholipase C and mobilizes intracellular calcium in primary cultures of sheep anterior pituitary cells. FEBS Lett. 243, 333 – 336. | en_US |
dc.identifier.citedreference | Van Dongen C. J., Zwiers H., and Gispen W. H. ( 1984 ) Purification and partial characterization of the phosphatidylinositol 4-phosphate kinase from rat brain. Biochem. J. 223, 197 – 203. | en_US |
dc.identifier.citedreference | Van Hooff C. O. M., De Graan P. N. E., Oestreicher A. B., and Gispen W. H. ( 1988 ) B-50 phosphorylation and polyphospho-inositide metabolism in nerve growth cone membranes. J. Neurosci. 8, 1789 – 1795. | en_US |
dc.identifier.citedreference | Varney M. A., Rivera J., Lopez-Bernal A., and Watson S. P. ( 1990 ) Are there subtypes of the inositol 1,4,5-trisphosphate receptor ? Biochem. J. 269, 211 – 216. | en_US |
dc.identifier.citedreference | VolontÉ C. and Racker E. ( 1988 ) Lithium stimulation of membrane-bound phospholipase C from PC12 cells exposed to nerve growth factor. J. Neurochem. 51, 1163 – 1168. | en_US |
dc.identifier.citedreference | VolontÉ C., Parries G. S., and Racker E. ( 1988 ) Stimulation of inositol incorporation in lipids of PC12 cells by nerve growth factor and bradykinin. J. Neurochem. 51, 1156 – 1162. | en_US |
dc.identifier.citedreference | Wakui M., Potter B. V. L., and Petersen O. H. ( 1989 ) Pulsatile intracellular calcium release does not depend on fluctuations in inositol trisphosphate concentration. Nature 339, 317 – 320. | en_US |
dc.identifier.citedreference | Wallace M. A. and ClarÓ E. ( 1990 ) A novel role for dopamine: inhibition of muscarinic cholinergic-stimulated phosphoinositide hydrolysis in rat brain cortical membranes. Neurosci. Lett. 110, 155 – 161. | en_US |
dc.identifier.citedreference | Whitman M., Kaplan D., Roberts T., and Cantley L. ( 1987 ) Evidence for two distinct phosphatidylinositol kinases in fibroblasts. Biochem. J. 247, 165 – 174. | en_US |
dc.identifier.citedreference | Willcocks A. L., Cooke A. M., Potter B. V. L., and Nahorski S. R. ( 1987 ) Stereospecific recognition sites for [ 3 H]inositol (1,4,5)-trisphosphate in particulate preparations of rat cerebellum. Biochem. Biophys. Res. Commun. 146, 1071 – 1078. | en_US |
dc.identifier.citedreference | Willcocks A. L., Potter B. V. L., Cooke A. M., and Nahorski S. R. ( 1988 ) myo-Inositol(1,4,5)-triphosphorothionate binds to specific [ 3 H]inositol-(1,4,5)trisphosphate sites in rat cerebellum and is resistant to 5-phosphatase. Eur. J. Pharmacol. 155, 181 – 183. | en_US |
dc.identifier.citedreference | Wilson K. M. and Minneman K. P. ( 1990 ) Pertussis toxin inhibits norepinephrine-stimulated inositol phosphate formation in primary brain cell cultures. Mol. Pharmacol. 38, 274 – 281. | en_US |
dc.identifier.citedreference | Wilson K. M., Gilchrist S., and Minneman K. P. ( 1990 ) Comparison of Α 1 -adrenergic receptor-stimulated inositol phosphate formation in primary neuronal and glial cultures. J. Neurochem. 55, 691 – 697. | en_US |
dc.identifier.citedreference | Wojcikiewicz R. J. H. and Nahorski S. R. ( 1989 ) Phosphoinositide hydrolysis in permeabilized SH-SY5Y human neuroblastoma cells is inhibited by mastoparan. FEBS Lett. 247, 341 – 344. | en_US |
dc.identifier.citedreference | Wong Y.-H. H., Kalmbach S. J., Hartman B. K., and Sherman W. R. ( 1987 ) Immunohistochemical staining and enzyme activity measurements show myo-inositol-1-phosphate synthase to be localized in the vasculature of brain. J. Neurochem. 48, 1434 – 1442. | en_US |
dc.identifier.citedreference | Wood C. A. and Schofield J. G. ( 1989 ) The effects of thyrotropin-releasing hormone and potassium depolarization on phosphoinositide metabolism and cytoplasmic calcium in bovine pituitary cells. Biochim. Biophys. Acta 1013, 97 – 106. | en_US |
dc.identifier.citedreference | Worley P. F., Baraban J. M., Colvin J. S., and Snyder S. H. ( 1987a ) Inositol trisphosphate receptor localization in brain: variable stoichiometry with protein kinase C. Nature 325, 159 – 161. | en_US |
dc.identifier.citedreference | Worley P. F., Baraban J. M., Supattapone S., Wilson V. S., and Snyder S. H. ( 1987b ) Characterization of inositol trisphosphate receptor binding in brain. Regulation by pH and calcium. J. Biol. Chem. 262, 12132 – 12136. | en_US |
dc.identifier.citedreference | Worley P. F., Baraban J. M., and Snyder S. H. ( 1989 ) Inositol 1,4,5-trisphosphate receptor binding: autoradiographic localization in rat brain. J. Neurosci. 9, 339 – 346. | en_US |
dc.identifier.citedreference | Xu J. and Chuang D.-M. ( 1987a ) Muscarinic acetylcholine receptor-mediated phosphoinositide turnover in cultured cerebellar granule cells: desensitization by receptor agonists. J. Pharmacol. Exp. Ther. 242, 238 – 242. | en_US |
dc.identifier.citedreference | Xu J. and Chuang D.-M. ( 1987b ) Serotonergic, adrenergic and histaminergic receptors coupled to phospholipase C in cultured cerebellar granule cells of rats. Biochem. Pharmacol. 36, 2353 – 2358. | en_US |
dc.identifier.citedreference | Yamakawa A. and Takenawa T. ( 1988 ) Purification and characterization of membrane-bound phosphatidylinositol kinase from rat brain. J. Biol. Chem. 263, 17555 – 17560. | en_US |
dc.identifier.citedreference | Yu O. and Chuang D.-M. ( 1988 ) GABA pretreatment enhances glutamate mediated phosphoinositide hydrolysis in neurons. Eur. J. Pharmacol. 158, 179 – 180. | en_US |
dc.identifier.citedreference | Zhang W., Sakai N., Yamada H., Fu T., and Nozawa Y. ( 1990 ) Endothelin-1 induces intracellular calcium rise and inositol 1,4,5-trisphosphate formation in cultured rat and human glioma cells. Neurosci. Lett. 112, 199 – 204. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.