MRTF-A alleviates myocardial ischemia reperfusion injury by inhibiting the inflammatory response and inducing autophagy

Mol Cell Biochem. 2023 Feb;478(2):343-359. doi: 10.1007/s11010-022-04510-4. Epub 2022 Jul 12.

Abstract

Myocardin-related transcription factor A (MRTF-A) has an inhibitory effect on myocardial infarction; however, the mechanism is not clear. This study reveals the mechanism by which MRTF-A regulates autophagy to alleviate myocardial infarct-mediated inflammation, and the effect of silent information regulator 1 (SIRT1) on the myocardial protective effect of MRTF-A was also verified. MRTF-A significantly decreased cardiac damage induced by myocardial ischemia. In addition, MRTF-A decreased NLRP3 inflammasome activity, and significantly increased the expression of autophagy protein in myocardial ischemia tissue. Lipopolysaccharide (LPS) and 3-methyladenine (3-MA) eliminated the protective effects of MRTF-A. Furthermore, simultaneous overexpression of MRTF-A and SIRT1 effectively reduced the injury caused by myocardial ischemia; this was associated with downregulation of inflammatory factor proteins and when upregulation of autophagy-related proteins. Inhibition of SIRT1 activity partially suppressed these MRTF-A-induced cardioprotective effects. SIRT1 has a synergistic effect with MRTF-A to inhibit myocardial ischemia injury through reducing the inflammation response and inducing autophagy.

Keywords: Autophagy; Inflammation; MRTF-A; Myocardial ischemia; SIRT1.

MeSH terms

  • Animals
  • Apoptosis
  • Autophagy
  • Inflammation
  • Myocardial Infarction*
  • Myocardial Ischemia*
  • Myocardial Reperfusion Injury* / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury*
  • Sirtuin 1 / genetics
  • Sirtuin 1 / metabolism

Substances

  • myocardin
  • Sirtuin 1