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The cytosolic splicing variant of NELL2 inhibits PKC beta 1 in glial cells

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dc.contributor.authorLee, Da Yong-
dc.contributor.authorKim, Eunju-
dc.contributor.authorLee, Young-Sun-
dc.contributor.authorRyu, Hwani-
dc.contributor.authorPark, Jae-Yong-
dc.contributor.authorHwang, Eun Mi-
dc.date.accessioned2021-09-05T02:50:25Z-
dc.date.available2021-09-05T02:50:25Z-
dc.date.created2021-06-15-
dc.date.issued2014-11-21-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/96745-
dc.description.abstractNELL2 is an abundant glycoprotein containing EGF-like domain in the neural tissues where it has multiple physiological functions by interacting with protein kinase C (PKC). There are two different splicing variant forms of NELL2 identified so far. One is secreted NELL2 (sNELL2) which is a neuron-specific variant and the other is cytosolic NELL2 (cNELL2) which is non-secreted splicing variant of NELL2. Although cNELL2 structure was well characterized, the expression pattern or the cellular function of cNELL2 is not fully determined. In this study, we found that cNELL2 specifically interacts with PKC beta isotypes and inhibits PKC beta 1 through direct binding to the N-terminal pseudosubstrate domain of PKC beta 1. Here, we also demonstrate that cNELL2 is predominantly expressed and has inhibitory effects on the PKC downstream signaling pathways in astrocytes thereby establishing cNELL2 as an endogenous inhibitor of PKCB1 in glia. (C) 2014 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectPROTEIN-KINASE-C-
dc.subjectACTIVATION-
dc.subjectBETA-
dc.subjectASTROCYTES-
dc.subjectEXPRESSION-
dc.subjectISOFORMS-
dc.subjectRELEASE-
dc.subjectMICE-
dc.titleThe cytosolic splicing variant of NELL2 inhibits PKC beta 1 in glial cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Jae-Yong-
dc.identifier.doi10.1016/j.bbrc.2014.10.110-
dc.identifier.scopusid2-s2.0-84910112554-
dc.identifier.wosid000346690600018-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.454, no.3, pp.459 - 464-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume454-
dc.citation.number3-
dc.citation.startPage459-
dc.citation.endPage464-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusPROTEIN-KINASE-C-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusBETA-
dc.subject.keywordPlusASTROCYTES-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusISOFORMS-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusMICE-
dc.subject.keywordAuthorNELL2-
dc.subject.keywordAuthorCytosolic NELL2-
dc.subject.keywordAuthorPKC beta 1-
dc.subject.keywordAuthorAstrocytes-
dc.subject.keywordAuthorPseudosubstrate domain-
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