Small Molecules Enable Cardiac Reprogramming of Mouse Fibroblasts with a Single Factor, Oct4
It was recently shown that mouse fibroblasts could be reprogrammed into cells of a cardiac fate by forced expression of multiple transcription factors and microRNAs. For ultimate application of such a reprogramming strategy for cell-based therapy or in vivo cardiac regeneration, reducing or eliminat...
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doaj-48bc8f73fa954c69927ba626f21cb0db2020-11-24T21:47:23ZengElsevierCell Reports2211-12472014-03-016595196010.1016/j.celrep.2014.01.038Small Molecules Enable Cardiac Reprogramming of Mouse Fibroblasts with a Single Factor, Oct4Haixia Wang0Nan Cao1C. Ian Spencer2Baoming Nie3Tianhua Ma4Tao Xu5Yu Zhang6Xiaojing Wang7Deepak Srivastava8Sheng Ding9Gladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAGladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USAIt was recently shown that mouse fibroblasts could be reprogrammed into cells of a cardiac fate by forced expression of multiple transcription factors and microRNAs. For ultimate application of such a reprogramming strategy for cell-based therapy or in vivo cardiac regeneration, reducing or eliminating the genetic manipulations by small molecules would be highly desirable. Here, we report the identification of a defined small-molecule cocktail that enables the highly efficient conversion of mouse fibroblasts into cardiac cells with only one transcription factor, Oct4, without any evidence of entrance into the pluripotent state. Small-molecule-induced cardiomyocytes spontaneously contract and exhibit a ventricular phenotype. Furthermore, these induced cardiomyocytes pass through a cardiac progenitor stage. This study lays the foundation for future pharmacological reprogramming approaches and provides a small-molecule condition for investigation of the mechanisms underlying the cardiac reprogramming process.http://www.sciencedirect.com/science/article/pii/S2211124714000722 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Haixia Wang Nan Cao C. Ian Spencer Baoming Nie Tianhua Ma Tao Xu Yu Zhang Xiaojing Wang Deepak Srivastava Sheng Ding |
spellingShingle |
Haixia Wang Nan Cao C. Ian Spencer Baoming Nie Tianhua Ma Tao Xu Yu Zhang Xiaojing Wang Deepak Srivastava Sheng Ding Small Molecules Enable Cardiac Reprogramming of Mouse Fibroblasts with a Single Factor, Oct4 Cell Reports |
author_facet |
Haixia Wang Nan Cao C. Ian Spencer Baoming Nie Tianhua Ma Tao Xu Yu Zhang Xiaojing Wang Deepak Srivastava Sheng Ding |
author_sort |
Haixia Wang |
title |
Small Molecules Enable Cardiac Reprogramming of Mouse Fibroblasts with a Single Factor, Oct4 |
title_short |
Small Molecules Enable Cardiac Reprogramming of Mouse Fibroblasts with a Single Factor, Oct4 |
title_full |
Small Molecules Enable Cardiac Reprogramming of Mouse Fibroblasts with a Single Factor, Oct4 |
title_fullStr |
Small Molecules Enable Cardiac Reprogramming of Mouse Fibroblasts with a Single Factor, Oct4 |
title_full_unstemmed |
Small Molecules Enable Cardiac Reprogramming of Mouse Fibroblasts with a Single Factor, Oct4 |
title_sort |
small molecules enable cardiac reprogramming of mouse fibroblasts with a single factor, oct4 |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2014-03-01 |
description |
It was recently shown that mouse fibroblasts could be reprogrammed into cells of a cardiac fate by forced expression of multiple transcription factors and microRNAs. For ultimate application of such a reprogramming strategy for cell-based therapy or in vivo cardiac regeneration, reducing or eliminating the genetic manipulations by small molecules would be highly desirable. Here, we report the identification of a defined small-molecule cocktail that enables the highly efficient conversion of mouse fibroblasts into cardiac cells with only one transcription factor, Oct4, without any evidence of entrance into the pluripotent state. Small-molecule-induced cardiomyocytes spontaneously contract and exhibit a ventricular phenotype. Furthermore, these induced cardiomyocytes pass through a cardiac progenitor stage. This study lays the foundation for future pharmacological reprogramming approaches and provides a small-molecule condition for investigation of the mechanisms underlying the cardiac reprogramming process. |
url |
http://www.sciencedirect.com/science/article/pii/S2211124714000722 |
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