4.7 Review

Direct Reprogramming-The Future of Cardiac Regeneration?

Journal

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 16, Issue 8, Pages 17368-17393

Publisher

MDPI AG
DOI: 10.3390/ijms160817368

Keywords

direct reprogramming; transdifferentiation; Gata4; Mef2c; Tbx5 (GMT); induced cardiomyocytes (iCMs)

Funding

  1. Rusche Forschungsprojekt of the DSHF
  2. DGTHG
  3. Bayerische Forschungsstiftung [AZ-1012-12]
  4. Deutsche Stiftung fur Herzforschung [F/37/11]
  5. Deutsches Zentrum fur Herz Kreislauf Forschung [DZHK B 13-050A, DZHK B 14-013SE, DZHK B 15-005, DZHK B 15-039SE]
  6. Deutsche Forschungsgemeinschaft-Sachmittelantrag [KR3770/7-1, KR3770/9-1]

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Today, the only available curative therapy for end stage congestive heart failure (CHF) is heart transplantation. This therapeutic option is strongly limited by declining numbers of available donor hearts and by restricted long-term performance of the transplanted graft. The disastrous prognosis for CHF with its restricted therapeutic options has led scientists to develop different concepts of alternative regenerative treatment strategies including stem cell transplantation or stimulating cell proliferation of different cardiac cell types in situ. However, first clinical trials with overall inconsistent results were not encouraging, particularly in terms of functional outcome. Among other approaches, very promising ongoing pre-clinical research focuses on direct lineage conversion of scar fibroblasts into functional myocardium, termed direct reprogramming or transdifferentiation. This review seeks to summarize strategies for direct cardiac reprogramming including the application of different sets of transcription factors, microRNAs, and small molecules for an efficient generation of cardiomyogenic cells for regenerative purposes.

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