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TBX3 Knockdown Decreases Reprogramming Efficiency of Human Cells

TBX3 is a member of the T-box transcription factor family and is involved in the core pluripotency network. Despite this role in the pluripotency network, its contribution to the reprogramming process during the generation of human induced pluripotent stem cells remains elusive. In this respect, we...

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Autores principales: Klingenstein, Moritz, Raab, Stefanie, Achberger, Kevin, Kleger, Alexander, Liebau, Stefan, Linta, Leonhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677243/
https://www.ncbi.nlm.nih.gov/pubmed/26697078
http://dx.doi.org/10.1155/2016/6759343
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author Klingenstein, Moritz
Raab, Stefanie
Achberger, Kevin
Kleger, Alexander
Liebau, Stefan
Linta, Leonhard
author_facet Klingenstein, Moritz
Raab, Stefanie
Achberger, Kevin
Kleger, Alexander
Liebau, Stefan
Linta, Leonhard
author_sort Klingenstein, Moritz
collection PubMed
description TBX3 is a member of the T-box transcription factor family and is involved in the core pluripotency network. Despite this role in the pluripotency network, its contribution to the reprogramming process during the generation of human induced pluripotent stem cells remains elusive. In this respect, we performed reprogramming experiments applying TBX3 knockdown in human fibroblasts and keratinocytes. Knockdown of TBX3 in both somatic cell types decreased the reprogramming efficiencies in comparison to control cells but with unchanged reprogramming kinetics. The resulting iPSCs were indistinguishable from control cells and displayed a normal in vitro differentiation capacity by generating cells of all three germ layers comparable to the controls.
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spelling pubmed-46772432015-12-22 TBX3 Knockdown Decreases Reprogramming Efficiency of Human Cells Klingenstein, Moritz Raab, Stefanie Achberger, Kevin Kleger, Alexander Liebau, Stefan Linta, Leonhard Stem Cells Int Research Article TBX3 is a member of the T-box transcription factor family and is involved in the core pluripotency network. Despite this role in the pluripotency network, its contribution to the reprogramming process during the generation of human induced pluripotent stem cells remains elusive. In this respect, we performed reprogramming experiments applying TBX3 knockdown in human fibroblasts and keratinocytes. Knockdown of TBX3 in both somatic cell types decreased the reprogramming efficiencies in comparison to control cells but with unchanged reprogramming kinetics. The resulting iPSCs were indistinguishable from control cells and displayed a normal in vitro differentiation capacity by generating cells of all three germ layers comparable to the controls. Hindawi Publishing Corporation 2016 2015-11-30 /pmc/articles/PMC4677243/ /pubmed/26697078 http://dx.doi.org/10.1155/2016/6759343 Text en Copyright © 2016 Moritz Klingenstein et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Klingenstein, Moritz
Raab, Stefanie
Achberger, Kevin
Kleger, Alexander
Liebau, Stefan
Linta, Leonhard
TBX3 Knockdown Decreases Reprogramming Efficiency of Human Cells
title TBX3 Knockdown Decreases Reprogramming Efficiency of Human Cells
title_full TBX3 Knockdown Decreases Reprogramming Efficiency of Human Cells
title_fullStr TBX3 Knockdown Decreases Reprogramming Efficiency of Human Cells
title_full_unstemmed TBX3 Knockdown Decreases Reprogramming Efficiency of Human Cells
title_short TBX3 Knockdown Decreases Reprogramming Efficiency of Human Cells
title_sort tbx3 knockdown decreases reprogramming efficiency of human cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677243/
https://www.ncbi.nlm.nih.gov/pubmed/26697078
http://dx.doi.org/10.1155/2016/6759343
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