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Unimpaired formation of hormone-stimulated inositol triphosphate in human mesangial cells under hyperglycemic conditions

dc.contributor.authorGreenberg, Lawrenceen_US
dc.contributor.authorUrbanes, Aris Q.en_US
dc.contributor.authorShayman, James A.en_US
dc.date.accessioned2006-04-10T15:17:31Z
dc.date.available2006-04-10T15:17:31Z
dc.date.issued1992-03-20en_US
dc.identifier.citationGreenberg, Lawrence, Urbanes, Aris Q., Shayman, James A. (1992/03/20)."Unimpaired formation of hormone-stimulated inositol triphosphate in human mesangial cells under hyperglycemic conditions." Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1138(3): 229-235. <http://hdl.handle.net/2027.42/30148>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T1Y-47NVY1K-7P/2/0d2b1e3bae7ef2e4ba7c2433f9490c6fen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30148
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1312360&dopt=citationen_US
dc.description.abstractThe relationship between bulk cellular myo-inositol content and phosphatidylinositol metabolism was evaluated in a human mesangial cell line under euglycemic and hyperglycemic conditions. Mesangial cells maintained in high glucose medium displayed a concentration-dependent fall in myo-inositol as measured by gas-liquid chromatography. Measurements of phosphatidylinositol, phosphatidylinositol 4-monophosphate and phosphatidylinositol 4,5-biphosphate mass revealed slight but statistically insignificant increases in cells exposed to high glucose containing medium. CDP-diacylglycerol: myo-inositol 3-phosphatidylinositol transferase activity, measured in plasma membranes from mesangial cells grwon under control and hyperglycemic conditions, was kinetically similar with Michaelis constants (Km values) for myo-inositol of 2.9 and 2.1 mM, respectively. Finally hormone-stimulated intracellular calcium mobilization and myo-inositol 1,4,5-triphosphate mass was measured from mesangial cells grown under normal and hyperglycemic conditions. Both intracellular calcium and inositol triphosphate formation were unchanged in cells previously exposed to high glucose conditions (400 mg/dl) compared to cells grown under normal glucose concentration (100 mg/dl). These data indicate that bulk changes in myo-inositol induced by hyperglycemia are neither associated with alterations in basal levels of inositol containing glycerolipids nor with changes in hormone-stimulated calcium mobilization and inositol trisphosphate formation under conditions of short term changes in extracellular glucose.en_US
dc.format.extent682222 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleUnimpaired formation of hormone-stimulated inositol triphosphate in human mesangial cells under hyperglycemic conditionsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Neophrology, University of Michigan and Veterans Administration Medical Centers, Ann Arbor, MI, U.S.A.en_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Neophrology, University of Michigan and Veterans Administration Medical Centers, Ann Arbor, MI, U.S.A.en_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Neophrology, University of Michigan and Veterans Administration Medical Centers, Ann Arbor, MI, U.S.A.en_US
dc.identifier.pmid1312360en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30148/1/0000525.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0925-4439(92)90042-Len_US
dc.identifier.sourceBiochimica et Biophysica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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