YTHDF1-mediated m 6 A RNA regulation controls cardiomyocyte remodeling through KLF11–HIF1α

Cardiovascular disease remains the leading cause of mortality globally. Although cardiac hypertrophy initially serves as a compensatory adaptation to stress, physiological and pathological hypertrophy are governed by distinct mechanisms and lead to divergent outcomes. However, how cardiomyocytes differentially respond to diverse stimuli remains incompletely understood. Here, we demonstrate that YTHDF1-mediated RNA m 6 A regulation modulates cardiomyocyte metabolic adaptation under different stress conditions and, in this context, directs hypertrophic response toward distinct remodeling outcomes. Cardiomyocyte-specific YTHDF1 deficiency leads to maladaptive cardiac remodeling in response to swimming exercise and additionally exacerbates pathological cardiac remodeling under pressure overload stimulation in vivo. In vitro, YTHDF1 functions as a switch to regulate the type of cardiomyocyte hypertrophy in an RNA m 6 A-dependent manner. Mechanistically, the YTHDF1–KLF11–HIF1α axis contributes to metabolic adaptation during cardiomyocyte hypertrophy. Cardiac-specific overexpression of YTHDF1 alleviates pathological cardiac remodeling. Together, our findings reveal a previously unrecognized YTHDF1–KLF11–HIF1α regulatory pathway linking m 6 A RNA recognition to cardiomyocyte remodeling. These findings provide valuable insight into how m 6 A-dependent signaling coordinates stress-responsive cardiac adaptation and establish YTHDF1 as an important regulator of cardiomyocyte remodeling.