STAT3 for Cardiac Regenerative Medicine: Involvement in Stem Cell Biology, Pathophysiology, and Bioengineering

Int J Mol Sci. 2020 Mar 12;21(6):1937. doi: 10.3390/ijms21061937.

Abstract

Heart disease is the most common cause of death in developed countries, but the medical treatments for heart failure remain limited. In this context, the development of cardiac regeneration therapy for severe heart failure is important. Owing to their unique characteristics, including multiple differentiation and infinitive self-renewal, pluripotent stem cells can be considered as a novel source for regenerative medicine. Janus kinase/signal transducer and activator of transcription 3 (JAK/STAT3) signaling plays critical roles in the induction, maintenance, and differentiation of pluripotent stem cells. In the heart, JAK/STAT3 signaling has diverse cellular functions, including myocardial differentiation, cell cycle re-entry of matured myocyte after injury, and anti-apoptosis in pathological conditions. Therefore, regulating STAT3 activity has great potential as a strategy of cardiac regeneration therapy. In this review, we summarize the current understanding of STAT3, focusing on stem cell biology and pathophysiology, as they contribute to cardiac regeneration therapy. We also introduce a recently reported therapeutic strategy for myocardial regeneration that uses engineered artificial receptors that trigger endogenous STAT3 signal activation.

Keywords: JAK/STAT signaling; cardiomyocytes; differentiation; pluripotent stem cells; regenerative medicine.

Publication types

  • Review

MeSH terms

  • Animals
  • Bioengineering / methods
  • Cell Differentiation / physiology
  • Heart / physiopathology*
  • Humans
  • Myocardium / metabolism
  • Pluripotent Stem Cells / metabolism*
  • Pluripotent Stem Cells / physiology*
  • Regeneration / physiology*
  • Regenerative Medicine / methods*
  • STAT3 Transcription Factor / metabolism*

Substances

  • STAT3 Transcription Factor