Activation of muscarinic cholinergic receptors enhances the volume-sensitive efflux of myo-inositol from SH-SY5Y neuroblastoma cells
dc.contributor.author | Loveday, Danny | en_US |
dc.contributor.author | Heacock, Anne M. | en_US |
dc.contributor.author | Fisher, Stephen K. | en_US |
dc.date.accessioned | 2010-04-01T14:47:33Z | |
dc.date.available | 2010-04-01T14:47:33Z | |
dc.date.issued | 2003-10 | en_US |
dc.identifier.citation | Loveday, Danny; Heacock, Anne M.; Fisher, Stephen K. (2003). "Activation of muscarinic cholinergic receptors enhances the volume-sensitive efflux of myo-inositol from SH-SY5Y neuroblastoma cells." Journal of Neurochemistry 87(2): 476-486. <http://hdl.handle.net/2027.42/65241> | en_US |
dc.identifier.issn | 0022-3042 | en_US |
dc.identifier.issn | 1471-4159 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/65241 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=14511125&dopt=citation | en_US |
dc.description.abstract | A mechanism used by cells to regulate their volume under hypo-osmotic conditions is the release of organic osmolytes, one of which is myo-inositol. The possibility that activation of phospholipase-C-linked receptors can regulate this process has been examined for SH-SY5Y neuroblastoma cells. Incubation of cells with hypo-osmolar buffers (160–250 mOsm) led to a biphasic release of inositol which persisted for up to 4 h and could be inhibited by inclusion of anion channel blockers – results which indicate the involvement of a volume-sensitive organic anion channel. Inclusion of oxotremorine-M, a muscarinic cholinergic agonist, resulted in a marked increase (80–100%) in inositol efflux under hypo-osmotic, but not isotonic, conditions. This enhanced release, which was observed under all conditions of hypo-osmolarity tested, could be prevented by inclusion of atropine. Incubation of the cells with either the calcium ionophore, ionomycin, or the phorbol ester, phorbol 12-myristate 13-acetate, partially mimicked the stimulatory effect of muscarinic receptor activation when added singly, and fully when added together. The ability of oxotremorine-M to facilitate inositol release was inhibited by removal of extracellular calcium, depletion of intracellular calcium or down-regulation of protein kinase C. These results indicate that activation of muscarinic cholinergic receptors can regulate osmolyte release in this cell line. | en_US |
dc.format.extent | 541979 bytes | |
dc.format.extent | 3110 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Science Ltd | en_US |
dc.rights | 2003 International Society for Neurochemistry | en_US |
dc.subject.other | Calcium | en_US |
dc.subject.other | Muscarinic Cholinergic Receptors | en_US |
dc.subject.other | Myo-inositol | en_US |
dc.subject.other | Osmolyte | en_US |
dc.subject.other | Protein Kinase C | en_US |
dc.subject.other | Volume Regulation | en_US |
dc.title | Activation of muscarinic cholinergic receptors enhances the volume-sensitive efflux of myo-inositol from SH-SY5Y neuroblastoma cells | 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 | † Department of Pharmacology, University of Michigan, Ann Arbor, Michigan, USA | en_US |
dc.contributor.affiliationother | * Mental Health Research Institute | en_US |
dc.identifier.pmid | 14511125 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/65241/1/j.1471-4159.2003.02021.x.pdf | |
dc.identifier.doi | 10.1046/j.1471-4159.2003.02021.x | en_US |
dc.identifier.source | Journal of Neurochemistry | en_US |
dc.identifier.citedreference | Akiba S., Kato E., Sato T. and Fujii T. ( 1992 ) Biscoclaurine alkaloids inhibit receptor-mediated phospholipase A 2 activation probably through uncoupling of a GTP-binding protein from the enzyme in rat peritoneal mast cells. Biochem. Pharmacol. 44, 45 – 50. | en_US |
dc.identifier.citedreference | Andrew R. D. ( 1991 ) Seizure and acute osmotic change: clinical and neurophysiological aspects. J. Neurol. Sci. 101, 7 – 18. | en_US |
dc.identifier.citedreference | Bender A. S., Neary J. T. and Norenberg M. D. ( 1993 ) Role of phosphoinositide hydrolysis in astrocyte volume regulation. J. Neurochem. 61, 1506 – 1514. | 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 | BrÈs V., Hurbin A., Duvoid A., Orcel H., Moos F. C., Rabie A. and Hussy N. ( 2000 ) Pharmacological characterization of volume-sensitive, taurine permeable anion channels in rat supraoptic glial cells. Br. J. Pharmacol. 130, 1976 – 1982. | en_US |
dc.identifier.citedreference | Cedazo-MÍnguez A., Popescu B. O., Ankarcrona M., Nishimura T. and Cowburn R. ( 2002 ) The presenilin 1 δE9 mutation gives enhanced basal phospholipase C activity and a resultant increase in intracellular calcium concentrations. J. Biol. Chem. 277, 36646 – 36655. | 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 12–0-tetradecanoylphorbol-13-acetate or mezerein. J. Neurochem. 54, 1725 – 1734. | en_US |
dc.identifier.citedreference | Crepel V., Panenka W., Kelly M. E. and MacVicar B. A. ( 1998 ) Mitogen-activated protein and tyrosine kinases in the activation of astrocyte volume-activated chloride current. J. Neurosci. 18, 1196 – 1206. | en_US |
dc.identifier.citedreference | De Sarno P., Shestopal S. A., King T. D., Zmijewska A., Song L. and Jope R. S. ( 2003 ) Muscarinic receptor activation protects cells from apoptotic effects of DNA damage, oxidative stress, and mitochondrial inhibition. J. Biol. Chem. 278, 11086 – 11093. | en_US |
dc.identifier.citedreference | Deleuze C., Duvoid A., Moos F. C. and Hussy N. ( 2000 ) Tyrosine phosphorylation modulates the osmosensitivity of volume-dependent taurine efflux from glial cells in the rat supraoptic nucleus. J. Physiol. 523, 291 – 299. | en_US |
dc.identifier.citedreference | Du X. Y. and Sorota S. ( 2000 ) Cardiac swelling-induced chloride current is enhanced by endothelin. J. Cardiovasc. Pharmacol. 35, 769 – 776. | en_US |
dc.identifier.citedreference | Fan H. T., Morishima S., Kida H. and Okada Y. ( 2001 ) Phloretin differentially inhibits volume-sensitive and cyclic AMP-activated, but not Ca-activated Cl – channels. Br. J. Pharmacol. 133, 1096 – 1106. | en_US |
dc.identifier.citedreference | Fisher S. K., Figueiredo J. C. and Bartus R. T. ( 1984 ) Differential stimulation of inositol phospholipid turnover in brain by analogs of oxotremorine. J. Neurochem. 43, 1171 – 1179. | 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 | Fisher S. K., Heacock A. M. and Agranoff B. W. ( 1992 ) Inositol lipids and signal transduction in the nervous system: an update. J. Neurochem. 58, 18 – 38. | en_US |
dc.identifier.citedreference | Fisher S. K., Novak J. E. and Agranoff B. W. ( 2002 ) Inositol and higher inositol phosphates in neural tissues: homeostasis, metabolism and functional significance. J. Neurochem. 82, 736 – 754. | en_US |
dc.identifier.citedreference | Fisher S. K., Loveday D., Heacock A. M. and Agranoff B. W. ( 2003 ) Muscarinic receptor activation regulates the volume-sensitive efflux of myo-inositol. Transactions of the 34th Annual Meeting of the American Society for Neurochemistry,. J. Neurochem. Suppl. 85, 46. | en_US |
dc.identifier.citedreference | Hale C. C. and Rubin L. J. ( 1995 ) Ion specificity and stoichiometry of the cardiac inositol transporter. J. Mol. Cell Cardiol. 27, 1123 – 1130. | en_US |
dc.identifier.citedreference | Haussinger D., Laubenberger J., vom Dahl S., Ernst T., Bayer S., Langer M., Gerok W. and Hennig J. ( 1994 ) Proton magnetic resonance spectroscopy studies on human brain myo-inositol in hypo-osmolarity and hepatic encephalopathy. Gastroenterology 107, 1475 – 1480. | en_US |
dc.identifier.citedreference | Honegger P. and Richelson E. ( 1976 ) Biochemical differentiation of mechanically dissociated mammalian brain in aggregating cell culture. Brain Res. 109, 335 – 354. | en_US |
dc.identifier.citedreference | Isaacks R. E., Bender A. S., Kim C. Y., Shi Y. F. and Norenberg M. D. ( 1999 ) Effect of osmolality and anion channel inhibitors on myo-inositol efflux in cultured astrocytes. J. Neurosci. Res. 57, 866 – 871. | en_US |
dc.identifier.citedreference | Jackson P. S. and Strange K. ( 1993 ) Volume-sensitive anion channels mediate swelling-activated inositol and taurine efflux. Am. J. Physiol. 265, C1489 – C1500. | en_US |
dc.identifier.citedreference | Kimelberg H. K. ( 2000 ) Cell volume in the CNS: regulation and implications for nervous system function and pathology. Neuroscientist 6, 14 – 25. | en_US |
dc.identifier.citedreference | Kwan C. Y., Takemura H., Obie J. F., Thastrup O. and Putney J. W. Jr ( 1990 ) Effects of MeCh, thapsigargin, and La 3+ on plasmalemmal and intracellular Ca 2+ transport in lacrimal acinar cells. Am. J. Physiol. 258, C1006 – C1015. | en_US |
dc.identifier.citedreference | Lambert D. G. and Nahorski S. R. ( 1990 ) Muscarinic-receptor-mediated changes in intracellular Ca 2+ and inositol 1,4,5-trisphosphate mass in a human neuroblastoma cell line, SH-SY5Y. Biochem. J. 265, 555 – 562. | en_US |
dc.identifier.citedreference | Lambert D. G., Challiss R. A. and Nahorski S. R. ( 1991 ) Accumulation and metabolism of Ins (1,4,5) P 3 and Ins (1,3,4,5) P 4 in muscarinic–receptor–stimulated SH–SY5Y neuroblastoma cells. Biochem. J. 273, 791 – 794. | en_US |
dc.identifier.citedreference | Lang F., Busch G. L., Ritter M., Volkl H., Waldegger S., Gulbins E. and Haussinger D. ( 1998 ) Functional significance of cell volume regulatory mechanisms. Physiol. Rev. 78, 247 – 306. | en_US |
dc.identifier.citedreference | Leaney J. L., Marsh S. J. and Brown D. A. ( 1997 ) A swelling-activated chloride current in rat sympathetic neurones. J. Physiol. 501, 555 – 564. | en_US |
dc.identifier.citedreference | Lee J. H., Arcinue E. and Ross B. D. ( 1994 ) Brief report: organic osmolytes in the brain of an infant with hypernatremia. N. Engl. J. Med. 331, 439 – 442. | en_US |
dc.identifier.citedreference | Lien Y. H., Shapiro J. I. and Chan L. ( 1990 ) Effects of hypernatremia on organic brain osmoles. J. Clin. Invest. 85, 1427 – 1435. | en_US |
dc.identifier.citedreference | Lien Y. H., Shapiro J. I. and Chan L. ( 1991 ) Study of brain electrolytes and organic osmolytes during correction of chronic hyponatremia. Implications for the pathogenesis of central pontine myelinolysis. J. Clin. Invest. 88, 303 – 309. | en_US |
dc.identifier.citedreference | Linseman D. A., McEwen E. L., Sorensen S. D. and Fisher S. K. ( 1998 ) Cytoskeletal and phosphoinositide requirements for muscarinic receptor signaling to focal adhesion kinase and paxillin. J. Neurochem. 70, 940 – 950. | en_US |
dc.identifier.citedreference | Linseman D. A., Hofmann F. and Fisher S. K. ( 2000 ) A role for the small molecular weight GTPases, Rho and Cdc42, in muscarinic receptor signaling to focal adhesion kinase. J. Neurochem. 74, 2010 – 2020. | en_US |
dc.identifier.citedreference | LÖhr J. W., McReynolds J., Grimaldi T. and Acara M. ( 1988 ) Effect of acute and chronic hypernatremia on myoinositol and sorbitol concentration in rat brain and kidney. Life Sci. 43, 271 – 276. | en_US |
dc.identifier.citedreference | Manolopoulos G. V., Prenen J., Droogmans G. and Nilius B. ( 1997 ) Thrombin potentiates volume-activated chloride currents in pulmonary artery endothelial cells. PflÜgers Arch. 433, 845 – 847. | en_US |
dc.identifier.citedreference | McManus M. L., Churchwell K. B. and Strange K. ( 1995 ) Regulation of cell volume in health and disease. N. Engl. J. Med. 333, 1260 – 1266. | en_US |
dc.identifier.citedreference | Mongin A. A. and Kimelberg H. K. ( 2002 ) ATP potently modulates anion channel-mediated excitatory amino acid release from cultured astrocytes. Am. J. Physiol. Cell Physiol. 283, C569 – C578. | en_US |
dc.identifier.citedreference | Mongin A. A., Reddi J. M., Charniga C. and Kimelberg H. K. ( 1999 ) [ 3 H]taurine and D-[ 3 H]aspartate release from astrocyte cultures are differently regulated by tyrosine kinases. Am. J. Physiol. 276, C1226 – C1230. | en_US |
dc.identifier.citedreference | Morales-Mulia S., Cardin V., Torres-Marquez M. E., Crevenna A. and Pasantes-Morales H. ( 2001 ) Influence of protein kinases on the osmosensitive release of taurine from cerebellar granule neurons. Neurochem. Int. 38, 153 – 161. | en_US |
dc.identifier.citedreference | Nilius B., Eggermont J., Voets T., Buyse G., Manolopoulos V. and Droogmans G. ( 1997 ) Properties of volume-regulated anion channels in mammalian cells. Prog. Biophys. Mol. Biol. 68, 69 – 119. | en_US |
dc.identifier.citedreference | Novak J. E., Turner R. S., Agranoff B. W. and Fisher S. K. ( 1999 ) Differentiated human NT2-N neurons possess a high intracellular content of myo-inositol. J. Neurochem. 72, 1431 – 1440. | en_US |
dc.identifier.citedreference | Novak J. E., Agranoff B. W. and Fisher S. K. ( 2000 ) Regulation of myo -inositol homeostasis in differentiated human NT2-N neurons. Neurochem. Res. 25, 561 – 566. | en_US |
dc.identifier.citedreference | Offermanns S., Bombien E. and Schultz G. ( 1993 ) Stimulation of tyrosine phosphorylation and mitogen-activated-protein (MAP) kinase activity in human SH-SY5Y neuroblastoma cells by carbachol. Biochem. J. 294, 545 – 550. | en_US |
dc.identifier.citedreference | Pandol S. J., Schoeffield M. S., Fimmel C. J. and Muallem S. ( 1987 ) The agonist-sensitive calcium pool in the pancreatic acinar cell. Activation of plasma membrane Ca 2+ influx mechanism. J. Biol. Chem. 262, 16963 – 16968. | en_US |
dc.identifier.citedreference | Pasantes-Morales H., Cardin V. and Tuz K. ( 2000 ) Signaling events during swelling and regulatory volume decrease. Neurochem. Res. 25, 1301 – 1314. | en_US |
dc.identifier.citedreference | Rosner H., Vacun G. and Rebhan M. ( 1995 ) Muscarinic receptor-mediated induction of actin-driven lamellar protrusions in neuroblastoma cell somata and growth cones. Involvement of protein kinase C. Eur. J. Cell Biol. 66, 324 – 334. | en_US |
dc.identifier.citedreference | Shuttleworth T. J. and Thompson J. L. ( 1999 ) Discriminating between capacitative and arachidonate-activated Ca 2+ entry pathways in HEK293 cells. J. Biol. Chem. 274, 31174 – 31178. | en_US |
dc.identifier.citedreference | Slowiejko D. M., Levey A. I. and Fisher S. K. ( 1994 ) Sequestration of muscarinic cholinergic receptors in permeabilized neuroblastoma cells. J. Neurochem. 62, 1795 – 1803. | en_US |
dc.identifier.citedreference | Sorensen S. D., Linseman D. A. and Fisher S. K. ( 1999 ) Distinct mechanisms for the endocytosis of muscarinic receptors and Gq/11. Eur. J. Pharmacol. 372, 325 – 328. | en_US |
dc.identifier.citedreference | Strange K., Morrison R., Shrode L. and Putnam R. ( 1993 ) Mechanism and regulation of swelling-activated inositol efflux in brain glial cells. Am. J. Physiol. 265, C244 – C256. | 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 | Thurston J. H., Sherman W. R., Hauhart R. E. and Kloepper R. F. ( 1989 ) myo-Inositol: a newly identified nonnitrogenous osmoregulatory molecule in mammalian brain. Pediatr. Res. 26, 482 – 485. | en_US |
dc.identifier.citedreference | Tsumura T., Oiki S., Ueda S., Okuma M. and Okada Y. ( 1996 ) Sensitivity of volume-sensitive Cl – conductance in human epithelial cells to extracellular nucleotides. Am. J. Physiol. 271, C1872 – C1878. | en_US |
dc.identifier.citedreference | Videen J. S., Michaelis T., Pinto P. and Ross B. D. ( 1995 ) Human cerebral osmolytes during chronic hyponatremia. A proton magnetic resonance spectroscopy study. J. Clin. Invest. 95, 788 – 793. | en_US |
dc.identifier.citedreference | Wilkinson S. E., Parker P. J. and Nixon J. S. ( 1993 ) Isoenzyme specificity of bisindolylmaleimides, selective inhibitors of protein kinase C. Biochem. J. 294, 335 – 337. | en_US |
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