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Proteome analysis of adipocyte lipid rafts reveals that gC1qR plays essential roles in adipogenesis and insulin signal transduction

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dc.contributor.authorKim, Ki-Bum-
dc.contributor.authorKim, Bong-Woo-
dc.contributor.authorChoo, Hyo-Jung-
dc.contributor.authorKwon, Young-Chan-
dc.contributor.authorAhn, Byung-Yoon-
dc.contributor.authorChoi, Jong-Soon-
dc.contributor.authorLee, Jae-Seon-
dc.contributor.authorKo, Young-Gyu-
dc.date.accessioned2021-09-08T17:39:32Z-
dc.date.available2021-09-08T17:39:32Z-
dc.date.issued2009-05-
dc.identifier.issn1615-9853-
dc.identifier.issn1615-9861-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120157-
dc.description.abstractSince insulin receptors and their downstream signaling molecules are organized in lipid rafts, proteomic analysis of adipocyte lipid rafts may provide new insights into the function of lipid rafts in adipogenesis and insulin signaling. To search for proteins involved in adipocyte differentiation and insulin signaling, we analyzed detergent-resistant lipid raft proteins from 3T3-L1 preadipocytes and adipocytes by 2-DE. Eleven raft proteins were identified from adipocytes. One of the adipocyte-specific proteins was globular C1q receptor (gC1qR), an acidic 32 kDa protein known as the receptor for the globular domain of complement C1q. The targeting of gC1qR into lipid rafts was significantly increased during adipogenesis, as determined by immunoblotting and immunofluorescence. Since the silencing of gC1qR by small RNA interference abolished adipogenesis and blocked insulin-induced activation of insulin receptor, insulin receptor substrate-1 (IRS-1), Akt, and Erk1/2, we can conclude that gC1qR is an essential molecule involved in adipogenesis and insulin signaling.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-
dc.titleProteome analysis of adipocyte lipid rafts reveals that gC1qR plays essential roles in adipogenesis and insulin signal transduction-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1002/pmic.200800811-
dc.identifier.scopusid2-s2.0-66249121051-
dc.identifier.wosid000266318800006-
dc.identifier.bibliographicCitationPROTEOMICS, v.9, no.9, pp 2373 - 2382-
dc.citation.titlePROTEOMICS-
dc.citation.volume9-
dc.citation.number9-
dc.citation.startPage2373-
dc.citation.endPage2382-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusATP SYNTHASE COMPLEX-
dc.subject.keywordPlusSTIMULATED GLUCOSE-UPTAKE-
dc.subject.keywordPlusCELLULAR-PROTEIN-
dc.subject.keywordPlusBINDING-PROTEIN-
dc.subject.keywordPlusKINASE-C-
dc.subject.keywordPlusRECEPTOR INHIBITOR-
dc.subject.keywordPlusPLASMA-MEMBRANE-
dc.subject.keywordPlusGLOBULAR HEADS-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusCAVEOLAE-
dc.subject.keywordAuthorInsulin resistance-
dc.subject.keywordAuthorLipid raft-
dc.subject.keywordAuthorSignal transduction-
dc.subject.keywordAuthorTwo-dimensional difference gel electrophoresis-
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