Reprogramming Roadblocks Are System Dependent
Since the first generation of induced pluripotent stem cells (iPSCs), several reprogramming systems have been used to study its molecular mechanisms. However, the system of choice largely affects the reprogramming efficiency, influencing our view on the mechanisms. Here, we demonstrate that reprogra...
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2015-09-01
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doaj-f0d7b17401954c348fd86c457e67511b2020-11-24T23:29:03ZengElsevierStem Cell Reports2213-67112015-09-015335036410.1016/j.stemcr.2015.07.007Reprogramming Roadblocks Are System DependentEleni Chantzoura0Stavroula Skylaki1Sergio Menendez2Shin-Il Kim3Anna Johnsson4Sten Linnarsson5Knut Woltjen6Ian Chambers7Keisuke Kaji8MRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh EH16 4UU, ScotlandDepartment of Biosystems Science and Engineering, ETH Zurich, 4058 Basel, SwitzerlandMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh EH16 4UU, ScotlandCenter for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto 606-8507, JapanLaboratory for Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Scheeles väg 1, 171 77 Stockholm, SwedenLaboratory for Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Scheeles väg 1, 171 77 Stockholm, SwedenCenter for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto 606-8507, JapanMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh EH16 4UU, ScotlandMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh EH16 4UU, ScotlandSince the first generation of induced pluripotent stem cells (iPSCs), several reprogramming systems have been used to study its molecular mechanisms. However, the system of choice largely affects the reprogramming efficiency, influencing our view on the mechanisms. Here, we demonstrate that reprogramming triggered by less efficient polycistronic reprogramming cassettes not only highlights mesenchymal-to-epithelial transition (MET) as a roadblock but also faces more severe difficulties to attain a pluripotent state even post-MET. In contrast, more efficient cassettes can reprogram both wild-type and Nanog−/− fibroblasts with comparable efficiencies, routes, and kinetics, unlike the less efficient reprogramming systems. Moreover, we attribute a previously reported variation in the N terminus of KLF4 as a dominant factor underlying these critical differences. Our data establish that some reprogramming roadblocks are system dependent, highlighting the need to pursue mechanistic studies with close attention to the systems to better understand reprogramming.http://www.sciencedirect.com/science/article/pii/S2213671115002131 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Eleni Chantzoura Stavroula Skylaki Sergio Menendez Shin-Il Kim Anna Johnsson Sten Linnarsson Knut Woltjen Ian Chambers Keisuke Kaji |
spellingShingle |
Eleni Chantzoura Stavroula Skylaki Sergio Menendez Shin-Il Kim Anna Johnsson Sten Linnarsson Knut Woltjen Ian Chambers Keisuke Kaji Reprogramming Roadblocks Are System Dependent Stem Cell Reports |
author_facet |
Eleni Chantzoura Stavroula Skylaki Sergio Menendez Shin-Il Kim Anna Johnsson Sten Linnarsson Knut Woltjen Ian Chambers Keisuke Kaji |
author_sort |
Eleni Chantzoura |
title |
Reprogramming Roadblocks Are System Dependent |
title_short |
Reprogramming Roadblocks Are System Dependent |
title_full |
Reprogramming Roadblocks Are System Dependent |
title_fullStr |
Reprogramming Roadblocks Are System Dependent |
title_full_unstemmed |
Reprogramming Roadblocks Are System Dependent |
title_sort |
reprogramming roadblocks are system dependent |
publisher |
Elsevier |
series |
Stem Cell Reports |
issn |
2213-6711 |
publishDate |
2015-09-01 |
description |
Since the first generation of induced pluripotent stem cells (iPSCs), several reprogramming systems have been used to study its molecular mechanisms. However, the system of choice largely affects the reprogramming efficiency, influencing our view on the mechanisms. Here, we demonstrate that reprogramming triggered by less efficient polycistronic reprogramming cassettes not only highlights mesenchymal-to-epithelial transition (MET) as a roadblock but also faces more severe difficulties to attain a pluripotent state even post-MET. In contrast, more efficient cassettes can reprogram both wild-type and Nanog−/− fibroblasts with comparable efficiencies, routes, and kinetics, unlike the less efficient reprogramming systems. Moreover, we attribute a previously reported variation in the N terminus of KLF4 as a dominant factor underlying these critical differences. Our data establish that some reprogramming roadblocks are system dependent, highlighting the need to pursue mechanistic studies with close attention to the systems to better understand reprogramming. |
url |
http://www.sciencedirect.com/science/article/pii/S2213671115002131 |
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