Gene therapy CM-YAPon protects the mouse heart from myocardial infarction

Nat Cardiovasc Res. 2025 Dec;4(12):1616-1626. doi: 10.1038/s44161-025-00744-9. Epub 2025 Nov 13.

Abstract

Myocardial infarction (MI) affects millions of people worldwide, causing irreversible injury to the heart and impairing cardiac function1. In both mouse and pig MI models, activating YAP in cardiomyocytes (CMs) stimulates regenerative repair2,3. Here we develop an adeno-associated virus 9-based therapy, termed CM-YAPon, which enables transient expression of an active YAP variant (YAP5SA) in CMs after exposure to the small molecule LMI070. A single LMI070 dose in mice triggers YAP5SA expression, CM cell cycle reentry and reprogramming of the cardiac microenvironment. YAP5SA induction after MI rapidly improves cardiac function while pre-MI induction confers cardioprotection and reduces cell death across multiple cardiac cell types. These findings reveal the therapeutic potential of reversible gene activation for ischemic heart disease.

MeSH terms

  • Adaptor Proteins, Signal Transducing* / genetics
  • Adaptor Proteins, Signal Transducing* / metabolism
  • Animals
  • Cell Cycle Proteins* / genetics
  • Cell Cycle Proteins* / metabolism
  • Dependovirus* / genetics
  • Disease Models, Animal
  • Genetic Therapy* / methods
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myocardial Infarction* / genetics
  • Myocardial Infarction* / metabolism
  • Myocardial Infarction* / pathology
  • Myocardial Infarction* / physiopathology
  • Myocardial Infarction* / prevention & control
  • Myocardial Infarction* / therapy
  • Myocytes, Cardiac* / drug effects
  • Myocytes, Cardiac* / metabolism
  • Myocytes, Cardiac* / pathology
  • Ventricular Function, Left
  • YAP-Signaling Proteins

Substances

  • YAP-Signaling Proteins
  • Yap1 protein, mouse
  • Adaptor Proteins, Signal Transducing
  • Cell Cycle Proteins