Please use this identifier to cite or link to this item: https://doi.org/10.1007/s10540-007-9051-2
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dc.titleCaspase inhibitor Z-VAD-FMK enhances the freeze-thaw survival rate of human embryonic stem cells
dc.contributor.authorHeng, B.C.
dc.contributor.authorClement, M.V.
dc.contributor.authorCao, T.
dc.date.accessioned2014-09-18T10:00:41Z
dc.date.available2014-09-18T10:00:41Z
dc.date.issued2007-10
dc.identifier.citationHeng, B.C., Clement, M.V., Cao, T. (2007-10). Caspase inhibitor Z-VAD-FMK enhances the freeze-thaw survival rate of human embryonic stem cells. Bioscience Reports 27 (4-5) : 257-264. ScholarBank@NUS Repository. https://doi.org/10.1007/s10540-007-9051-2
dc.identifier.issn01448463
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/79957
dc.description.abstractPrevious study demonstrated that the low survival of human embryonic stem cells (hESC) under conventional slow-cooling cryopreservation protocols is predominantly due to apoptosis rather than cellular necrosis. Hence, this study investigated whether a synthetic broad-spectrum irreversible inhibitor of caspase enzymes, Z-VAD-FMK can be used to enhance the post-thaw survival rate of hESC. About 100 mM Z-VAD-FMK was supplemented into either the freezing solution, the post-thaw culture media or both. Intact and adherent hESC colonies were cryopreserved so as to enable subsequent quantitation of the post-thaw cell survival rate through the MTT assay, which can only be performed with adherent cells. Exposure to 100 mM Z-VAD-FMK in the freezing solution alone did not significantly enhance the post-thaw survival rate (10.2% vs. 9.9%, p > 0.05). However, when 100 mM Z-VAD-FMK was added to the post-thaw culture media, there was a significant enhancement in the survival rate from 9.9% to 14.4% (p < 0.05), which was further increased to 18.7% when Z-VAD-FMK was also added to the freezing solution as well (p < 0.01). Spontaneous differentiation of hESC after cryopreservation was assessed by morphological observations under bright-field microscopy, and by immunocytochemical staining for the pluripotency markers SSEA-3 and TRA-1-81. The results demonstrated that exposure to Z-VAD-FMK did not significantly enhance the spontaneous differentiation of hESC within post-thaw culture. © 2007 The Biochemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s10540-007-9051-2
dc.sourceScopus
dc.subjectApoptosis
dc.subjectCryopreservation
dc.subjectEmbryonic
dc.subjectFreezing
dc.subjectHuman
dc.subjectInhibition
dc.subjectStem cells
dc.typeArticle
dc.contributor.departmentORAL AND MAXILLOFACIAL SURGERY
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1007/s10540-007-9051-2
dc.description.sourcetitleBioscience Reports
dc.description.volume27
dc.description.issue4-5
dc.description.page257-264
dc.description.codenBRPTD
dc.identifier.isiut000248762300005
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