Conversion of human fibroblasts into functional cardiomyocytes by small molecules

Author:

Cao Nan12,Huang Yu1,Zheng Jiashun34,Spencer C. Ian1,Zhang Yu12,Fu Ji-Dong5,Nie Baoming12,Xie Min12,Zhang Mingliang12,Wang Haixia12,Ma Tianhua12,Xu Tao12,Shi Guilai12,Srivastava Deepak163,Ding Sheng12

Affiliation:

1. Gladstone Institute of Cardiovascular Disease, San Francisco, CA 94158, USA.

2. Department of Pharmaceutical Chemistry, University of California–San Francisco, San Francisco, CA 94158, USA.

3. Department of Biochemistry and Biophysics, University of California–San Francisco, San Francisco, CA 94158, USA.

4. California Institute for Quantitative Biosciences, University of California–San Francisco, San Francisco, CA 94158, USA.

5. Department of Medicine, Heart and Vascular Research Center, Case Western Reserve University, Cleveland, OH 44106, USA.

6. Department of Pediatrics, University of California–San Francisco, San Francisco, CA 94158, USA.

Abstract

Making cardiac cells from fibroblasts Reprogramming noncardiac cells into functional cardiomyocytes without any genetic manipulation could open up new avenues for cardiac regenerative therapies. Cao et al. identified a combination of nine small molecules that could epigenetically activate human fibroblasts, efficiently reprogramming them into chemically induced cardiomyocytes (ciCMs). The ciCMs contracted uniformly and resembled human cardiomyocytes. This method may be adapted for reprogramming multiple cell types and have important implications in regenerative medicine. Science , this issue p. 1216

Funder

California Institute for Regenerative Medicine (CIRM)

American Heart Association

CIRM

National Heart, Lung, and Blood Institute

National Institutes of Health

Roddenberry Foundation

Younger Family Foundation

Whittier Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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