Please use this identifier to cite or link to this item: https://doi.org/10.7717/peerj.2695
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dc.titleInduced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning
dc.contributor.authorLim, S.J
dc.contributor.authorHo, S.C
dc.contributor.authorMok, P.L
dc.contributor.authorTan, K.L
dc.contributor.authorOng, A.H
dc.contributor.authorGan, S.C
dc.date.accessioned2020-11-10T08:06:09Z
dc.date.available2020-11-10T08:06:09Z
dc.date.issued2016
dc.identifier.citationLim, S.J, Ho, S.C, Mok, P.L, Tan, K.L, Ong, A.H, Gan, S.C (2016). Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning. PeerJ 2016 (11) : 2695. ScholarBank@NUS Repository. https://doi.org/10.7717/peerj.2695
dc.identifier.issn21678359
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/183368
dc.description.abstractBackground. Human hair follicles are important for the renewal of new hairs and their development. The generation of induced pluripotent stem cells (iPSCs) from hair follicles is easy due to its accessibility and availability. The pluripotent cells derived from hair follicles not only have a higher tendency to re-differentiate into hair follicles, but are also more suited for growth in hair scalp tissue microenvironment. Methods. In this study, human hair follicular keratinocytes were used to generate iPSCs, which were then further differentiated in vitro into keratinocytes. The derived iPSCs were characterised by using immunofluorescence staining, flow cytometry, and reverse-transcription PCR to check for its pluripotency markers expression. Results. The iPSC clones expressed pluripotency markers such as TRA-1-60, TRA-1-81, SSEA4, OCT4, SOX2, NANOG, LEFTY, and GABRB. The well-formed three germ layers were observed during differentiation using iPSCs derived from hair follicles. The successful formation of keratioctyes from iPSCs was confirmed by the expression of cytokeratin 14 marker. Discussion. Hair follicles represent a valuable keratinocytes source for in vitro hair cloning for use in treating hair balding or grafting in burn patients. Our significant findings in this report proved that hair follicles could be used to produce pluripotent stem cells and suggested that the genetic and micro-environmental elements of hair follicles might trigger higher and more efficient hair follicles re-differentiation. Copyright 2016 Lim et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectcell marker
dc.subjectcytokeratin 14
dc.subjectplasmid DNA
dc.subjectalopecia
dc.subjectArticle
dc.subjectburn
dc.subjectcell cloning
dc.subjectcell differentiation
dc.subjectcontrolled study
dc.subjectflow cytometry
dc.subjectgenetic transfection
dc.subjecthair follicle
dc.subjecthuman
dc.subjecthuman cell
dc.subjectimmunofluorescence
dc.subjectinduced pluripotent stem cell
dc.subjectkeratinocyte
dc.subjectmicroenvironment
dc.subjectprotein expression
dc.subjectreverse transcription polymerase chain reaction
dc.subjectscalp
dc.subjectviral gene delivery system
dc.typeArticle
dc.contributor.departmentDEPARTMENT OF COMPUTER SCIENCE
dc.description.doi10.7717/peerj.2695
dc.description.sourcetitlePeerJ
dc.description.volume2016
dc.description.issue11
dc.description.page2695
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