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Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning

BACKGROUND: 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...

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Autores principales: Lim, Sheng Jye, Ho, Shu Cheow, Mok, Pooi Ling, Tan, Kian Lee, Ong, Alan H.K., Gan, Seng Chiew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111897/
https://www.ncbi.nlm.nih.gov/pubmed/27867768
http://dx.doi.org/10.7717/peerj.2695
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author Lim, Sheng Jye
Ho, Shu Cheow
Mok, Pooi Ling
Tan, Kian Lee
Ong, Alan H.K.
Gan, Seng Chiew
author_facet Lim, Sheng Jye
Ho, Shu Cheow
Mok, Pooi Ling
Tan, Kian Lee
Ong, Alan H.K.
Gan, Seng Chiew
author_sort Lim, Sheng Jye
collection PubMed
description BACKGROUND: 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.
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spelling pubmed-51118972016-11-18 Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning Lim, Sheng Jye Ho, Shu Cheow Mok, Pooi Ling Tan, Kian Lee Ong, Alan H.K. Gan, Seng Chiew PeerJ Cell Biology BACKGROUND: 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. PeerJ Inc. 2016-11-10 /pmc/articles/PMC5111897/ /pubmed/27867768 http://dx.doi.org/10.7717/peerj.2695 Text en ©2016 Lim et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Cell Biology
Lim, Sheng Jye
Ho, Shu Cheow
Mok, Pooi Ling
Tan, Kian Lee
Ong, Alan H.K.
Gan, Seng Chiew
Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning
title Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning
title_full Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning
title_fullStr Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning
title_full_unstemmed Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning
title_short Induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning
title_sort induced pluripotent stem cells from human hair follicle keratinocytes as a potential source for in vitro hair follicle cloning
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111897/
https://www.ncbi.nlm.nih.gov/pubmed/27867768
http://dx.doi.org/10.7717/peerj.2695
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