Molecular Therapy: Nucleic Acids (Sep 2022)

Aberrant HSF1 signaling activation underlies metformin amelioration of myocardial infarction in mice

  • Mingyuan Wang,
  • Jiang Zou,
  • Jinjin Wang,
  • Meidong Liu,
  • Ke Liu,
  • Nian Wang,
  • Kangkai Wang

Journal volume & issue
Vol. 29
pp. 312 – 328

Abstract

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Myocardial infarction (MI) is a cardiovascular disease with high morbidity and mortality. Clinically, rehabilitation after massive MI often has a poor prognosis. Therefore, it is necessary to explore the therapeutic methods of myocardial protection after MI. As a first-line treatment for type 2 diabetes, metformin has been found to have a certain protective effect on myocardial tissue. However, its pharmacological mechanism remains unclear. In this study, we investigated key factors that reduced MI with metformin. Through in vivo, in vitro, and in silico analyses, we identified HSF1 as a key target for metformin. HSF1 could up-regulate the transcriptional level of AMPKα2 through transcriptional activation and stimulate the activity of the downstream AMPK/mTOR signaling pathway. Metformin stimulated cardiomyocytes to form stress granules (SGs), and knockdown of HSF1 reversed this process. Furthermore, HSF1 exhibited better in vitro affinity for metformin than AMPK, suggesting that HSF1 may be a more sensitive target for metformin.

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