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Cited 49 time in webofscience Cited 51 time in scopus
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dc.contributor.authorJUNG-MIN KIM-
dc.contributor.authorKim, JM-
dc.contributor.authorKim, YH-
dc.contributor.authorKim, KT-
dc.contributor.authorRyu, SH-
dc.contributor.authorLee, TG-
dc.contributor.authorSuh, PG-
dc.date.accessioned2016-03-31T08:36:24Z-
dc.date.available2016-03-31T08:36:24Z-
dc.date.created2013-01-31-
dc.date.issued2013-01-
dc.identifier.issn0021-9541-
dc.identifier.other2013-OAK-0000027339-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/15642-
dc.description.abstractOsteogenesis is a tightly regulated process that involves coordinated extracellular signals from autocrine and paracrine loops. Secretory proteins during osteogenesis can inhibit cell proliferation and activate cell differentiation toward mature osteoblasts, which are characterized by mineralization. In this study, we attempted to identify these secretory proteins during osteogenesis using LCMS/MS analysis. We compared the secretome between undifferentiated human bone marrow-derived mesenchymal stem cells (hBMSCs) and differentiated osteoblasts. Among 315 proteins that were identified, 177 proteins were present at increased levels in osteoblasts, whereas 88 proteins were present at decreased levels. Among the identified proteins, several were validated by quantitative RT-PCR and immunoblot analysis. Of particular interest, calcium homeostasis-related proteins were upregulated, whereas stem cell proliferation-related proteins and other lineage-related proteins were downregulated during osteogenesis. These findings provide information about the dynamic changes in the expression and secretion of proteins during osteogenesis and suggest the putative role of secretory proteins in osteogenesis. J. Cell. Physiol. 228: 216224, 2013. (c) 2012 Wiley Periodicals, Inc.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherJOURNAL OF CELLULAR PHYSIOLOGY-
dc.relation.isPartOfJOURNAL OF CELLULAR PHYSIOLOGY-
dc.titleComparative secretome analysis of human bone marrow-derived mesenchymal stem cells during osteogenesis-
dc.typeArticle-
dc.contributor.college융합생명공학부-
dc.identifier.doi10.1002/JCP.24123-
dc.author.googleKim, JM-
dc.author.googleKim, J-
dc.author.googleKim, YH-
dc.author.googleKim, KT-
dc.author.googleRyu, SH-
dc.author.googleLee, TG-
dc.author.googleSuh, PG-
dc.relation.volume228-
dc.relation.issue1-
dc.relation.startpage216-
dc.relation.lastpage224-
dc.contributor.id10104775-
dc.relation.journalJOURNAL OF CELLULAR PHYSIOLOGY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF CELLULAR PHYSIOLOGY, v.228, no.1, pp.216 - 224-
dc.identifier.wosid000309678000026-
dc.date.tcdate2019-01-01-
dc.citation.endPage224-
dc.citation.number1-
dc.citation.startPage216-
dc.citation.titleJOURNAL OF CELLULAR PHYSIOLOGY-
dc.citation.volume228-
dc.contributor.affiliatedAuthorKim, KT-
dc.contributor.affiliatedAuthorRyu, SH-
dc.identifier.scopusid2-s2.0-84866442528-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc22-
dc.description.scptc25*
dc.date.scptcdate2018-05-121*
dc.description.isOpenAccessN-
dc.type.docTypeArticle-
dc.subject.keywordPlusGROWTH-FACTOR-BETA-
dc.subject.keywordPlusSERUM CYSTATIN-C-
dc.subject.keywordPlusPROTEOMIC ANALYSIS-
dc.subject.keywordPlusMATRIX VESICLES-
dc.subject.keywordPlusADIPOSE-TISSUE-
dc.subject.keywordPlusTGF-BETA-
dc.subject.keywordPlusACTIVATOR INHIBITOR-1-
dc.subject.keywordPlusNUCLEAR TRANSLOCATION-
dc.subject.keywordPlusALKALINE-PHOSPHATASE-
dc.subject.keywordPlusMINERAL DEPOSITION-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaPhysiology-

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류성호RYU, SUNG HO
Dept of Life Sciences
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