Abstract
Myocardial infarction (MI) affects millions of people worldwide, causing irreversible injury to the heart and impairing cardiac function(1). In both mouse and pig MI models, activating YAP in cardiomyocytes (CMs) stimulates regenerative repair(2,3). Here we develop an adeno-associated virus 9-based therapy, termed CM-YAP(on), 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.