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...

Full description

Bibliographic Details
Main Authors: Haixia Wang, Nan Cao, C. Ian Spencer, Baoming Nie, Tianhua Ma, Tao Xu, Yu Zhang, Xiaojing Wang, Deepak Srivastava, Sheng Ding
Format: Article
Language:English
Published: Elsevier 2014-03-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124714000722
id doaj-48bc8f73fa954c69927ba626f21cb0db
record_format Article
spelling 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
work_keys_str_mv AT haixiawang smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT nancao smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT cianspencer smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT baomingnie smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT tianhuama smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT taoxu smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT yuzhang smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT xiaojingwang smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT deepaksrivastava smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
AT shengding smallmoleculesenablecardiacreprogrammingofmousefibroblastswithasinglefactoroct4
_version_ 1725897402391461888