Loss of lipin1 disrupts heart muscle membrane integrity, driving inflammation, fibrosis, and contributing to heart failure.
BackgroundLipin1 has dual functions acting as phosphatidic acid phosphatase required for lipid synthesis and as a transcriptional coactivator. Our previous research demonstrated that lipin1 is critical for maintaining sarcolemmal integrity in skeletal muscle. Given the importance of sarcolemmal stability for cardiac muscle viability and function, we investigated the role of lipin1 in the heart using a novel cardiac‐specific lipin1 deficient (Myh6‐lipin 1−/−) mouse model.








