Induction of Pluripotency in Adult Equine Fibroblasts without c-MYC

Despite tremendous efforts on isolation of pluripotent equine embryonic stem (ES) cells, to date there are few reports about successful isolation of ESCs and no report of in vivo differentiation of this important companion species. We report the induction of pluripotency in adult equine fibroblasts...

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Main Authors: Khodadad Khodadadi, Huseyin Sumer, Maryam Pashaiasl, Susan Lim, Mark Williamson, Paul J. Verma
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2012/429160
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spelling doaj-dca6744a7df14ae7978bd9b6af3cee5c2020-11-24T21:29:50ZengHindawi LimitedStem Cells International1687-966X1687-96782012-01-01201210.1155/2012/429160429160Induction of Pluripotency in Adult Equine Fibroblasts without c-MYCKhodadad Khodadadi0Huseyin Sumer1Maryam Pashaiasl2Susan Lim3Mark Williamson4Paul J. Verma5Centre for Reproduction and Development, Monash Institute of Medical Research, Monash University, Clayton, VIC 3800, AustraliaCentre for Reproduction and Development, Monash Institute of Medical Research, Monash University, Clayton, VIC 3800, AustraliaCentre for Reproduction and Development, Monash Institute of Medical Research, Monash University, Clayton, VIC 3800, AustraliaStem Cell Technologies i (SCTi), Gleneagles Medical Centre, 258499, SingaporeGribbles Veterinary, Clayton, VIC 3168, AustraliaCentre for Reproduction and Development, Monash Institute of Medical Research, Monash University, Clayton, VIC 3800, AustraliaDespite tremendous efforts on isolation of pluripotent equine embryonic stem (ES) cells, to date there are few reports about successful isolation of ESCs and no report of in vivo differentiation of this important companion species. We report the induction of pluripotency in adult equine fibroblasts via retroviral transduction with three transcription factors using OCT4, SOX2, and KLF4 in the absence of c-MYC. The cell lines were maintained beyond 27 passages (more than 11 months) and characterized. The equine iPS (EiPS) cells stained positive for alkaline phosphatase by histochemical staining and expressed OCT4, NANOG, SSEA1, and SSEA4. Gene expression analysis of the cells showed the expression of OCT4, SOX2 NANOG, and STAT3. The cell lines retained a euploid chromosome count of 64 after long-term culture cryopreservation. The EiPS demonstrated differentiation capacity for the three embryonic germ layers both in vitro by embryoid bodies (EBs) formation and in vivo by teratoma formation. In conclusion, we report the derivation of iPS cells from equine adult fibroblasts and long-term maintenance using either of the three reprogramming factors.http://dx.doi.org/10.1155/2012/429160
collection DOAJ
language English
format Article
sources DOAJ
author Khodadad Khodadadi
Huseyin Sumer
Maryam Pashaiasl
Susan Lim
Mark Williamson
Paul J. Verma
spellingShingle Khodadad Khodadadi
Huseyin Sumer
Maryam Pashaiasl
Susan Lim
Mark Williamson
Paul J. Verma
Induction of Pluripotency in Adult Equine Fibroblasts without c-MYC
Stem Cells International
author_facet Khodadad Khodadadi
Huseyin Sumer
Maryam Pashaiasl
Susan Lim
Mark Williamson
Paul J. Verma
author_sort Khodadad Khodadadi
title Induction of Pluripotency in Adult Equine Fibroblasts without c-MYC
title_short Induction of Pluripotency in Adult Equine Fibroblasts without c-MYC
title_full Induction of Pluripotency in Adult Equine Fibroblasts without c-MYC
title_fullStr Induction of Pluripotency in Adult Equine Fibroblasts without c-MYC
title_full_unstemmed Induction of Pluripotency in Adult Equine Fibroblasts without c-MYC
title_sort induction of pluripotency in adult equine fibroblasts without c-myc
publisher Hindawi Limited
series Stem Cells International
issn 1687-966X
1687-9678
publishDate 2012-01-01
description Despite tremendous efforts on isolation of pluripotent equine embryonic stem (ES) cells, to date there are few reports about successful isolation of ESCs and no report of in vivo differentiation of this important companion species. We report the induction of pluripotency in adult equine fibroblasts via retroviral transduction with three transcription factors using OCT4, SOX2, and KLF4 in the absence of c-MYC. The cell lines were maintained beyond 27 passages (more than 11 months) and characterized. The equine iPS (EiPS) cells stained positive for alkaline phosphatase by histochemical staining and expressed OCT4, NANOG, SSEA1, and SSEA4. Gene expression analysis of the cells showed the expression of OCT4, SOX2 NANOG, and STAT3. The cell lines retained a euploid chromosome count of 64 after long-term culture cryopreservation. The EiPS demonstrated differentiation capacity for the three embryonic germ layers both in vitro by embryoid bodies (EBs) formation and in vivo by teratoma formation. In conclusion, we report the derivation of iPS cells from equine adult fibroblasts and long-term maintenance using either of the three reprogramming factors.
url http://dx.doi.org/10.1155/2012/429160
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