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Directed transdifferentiation of mouse mesoderm to heart tissue by defined factors

Author

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  • Jun K. Takeuchi

    (Gladstone Institute of Cardiovascular Disease, San Francisco, California 94158, USA
    Global-Edge Institute, Tokyo Institute of Technology, Frontier S2-16, Nagatsuda, Midori-ku, Yokohama, Kanagawa 226-8503, Japan)

  • Benoit G. Bruneau

    (Gladstone Institute of Cardiovascular Disease, San Francisco, California 94158, USA
    Cardiovascular Research Institute, and Institute for Regeneration Medicine, University of California, San Francisco, California 94158, USA)

Abstract

Heart-cell generation The heart has little regenerative capacity after damage, so understanding the factors required to produce new cardiac myocytes is of great interest. Jun Takeuchi and Benoit Bruneau have investigated the minimal requirements for transdifferentiation of mouse mesoderm to cardiac myocytes, and find that two cardiac transcription factors and a cardiac-specific subunit of BAF chromatin-remodelling complexes are sufficient to direct differentiation of mouse mesoderm into beating cardiomyocytes. Addition of a further transcription factor promotes differentiation into contracting cardiomyocytes, and repression of noncardiac mesodermal genes. Defining the requirements for cardiac cellular differentiation may help in the long-term goal of regenerating cardiomyocytes for therapies.

Suggested Citation

  • Jun K. Takeuchi & Benoit G. Bruneau, 2009. "Directed transdifferentiation of mouse mesoderm to heart tissue by defined factors," Nature, Nature, vol. 459(7247), pages 708-711, June.
  • Handle: RePEc:nat:nature:v:459:y:2009:i:7247:d:10.1038_nature08039
    DOI: 10.1038/nature08039
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    Cited by:

    1. Yinuo Wang & Adel Elsherbiny & Linda Kessler & Julio Cordero & Haojie Shi & Heike Serke & Olga Lityagina & Felix A. Trogisch & Mona Malek Mohammadi & Ibrahim El-Battrawy & Johannes Backs & Thomas Wiel, 2022. "Lamin A/C-dependent chromatin architecture safeguards naïve pluripotency to prevent aberrant cardiovascular cell fate and function," Nature Communications, Nature, vol. 13(1), pages 1-24, December.

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