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Cited 12 time in webofscience Cited 12 time in scopus
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dc.contributor.authorAng Joshur-
dc.contributor.authorLee Yong-An-
dc.contributor.authorRaghothaman Deepak-
dc.contributor.authorPremkumar Jayaraman-
dc.contributor.authorTeo Kim L-
dc.contributor.authorKhan Fahima J-
dc.contributor.authorReuveny Shaul-
dc.contributor.authorCHANG, YOUNG TAE-
dc.contributor.authorKANG, NAMYOUNG-
dc.contributor.authorOh Steve-
dc.date.accessioned2019-12-18T08:10:17Z-
dc.date.available2019-12-18T08:10:17Z-
dc.date.created2019-12-17-
dc.date.issued2019-10-
dc.identifier.issn1860-6768-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/100529-
dc.description.abstractDespite intense interest in human mesenchymal stromal cells (MSCs), monitoring of the progressive occurrence of senescence has been hindered by the lack of efficient detection tools. Here, the discovery of a novel MSC senescence‐specific fluorescent probe (CyBC9) identified by a high‐throughput screen is reported. Compared with the prototypical senescence‐associated β‐galactosidase (SA‐β‐gal) staining, the CyBC9 assay is rapid (2 h) and nontoxic and can thus be applied to live cells. It is shown that CyBC9 is able to stain early and late senescent populations both in monolayer‐ and in microcarrier‐based cultures. Finally, to investigate the mechanism of CyBC9, colocalization assays are performed and it is found that CyBC9 is accumulated in the mitochondria of senescent MSCs presumably due to the loss of membrane potential. Taken together, it is expected that CyBC9 will be a useful tool to ameliorate cell therapy through rapid and early screening of senescent phenotypes in clinically relevant MSCs.-
dc.languageEnglish-
dc.publisherWiley - VCH Verlag GmbH & CO. KGaA-
dc.relation.isPartOfBiotechnology journal-
dc.titleRapid Detection of Senescent Mesenchymal Stromal Cells by a Fluorescent Probe-
dc.typeArticle-
dc.identifier.doi10.1002/biot.201800691-
dc.type.rimsART-
dc.identifier.bibliographicCitationBiotechnology journal, v.14, no.10, pp.1800691 - 1800691-
dc.identifier.wosid000478243700001-
dc.citation.endPage1800691-
dc.citation.number10-
dc.citation.startPage1800691-
dc.citation.titleBiotechnology journal-
dc.citation.volume14-
dc.contributor.affiliatedAuthorCHANG, YOUNG TAE-
dc.contributor.affiliatedAuthorKANG, NAMYOUNG-
dc.identifier.scopusid2-s2.0-85069924066-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.type.docTypeArticle-
dc.subject.keywordPlusLIBRARY APPROACH DOFLA-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusCULTURE-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusMICROCARRIERS-
dc.subject.keywordPlusFIBROBLASTS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusEXPANSION-
dc.subject.keywordPlusBIOMARKER-
dc.subject.keywordAuthorfluorescent probe-
dc.subject.keywordAuthormesenchymal stromal cells-
dc.subject.keywordAuthorsenescence-
dc.subject.keywordAuthorstem cells-
dc.subject.keywordAuthoraging-
dc.subject.keywordAuthorbioprocessing-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-

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