The immunoproteasome catalytic ?5i subunit regulates cardiac hypertrophy by targeting the autophagy protein ATG5 for degradation.

ABSTRACT: Pathological cardiac hypertrophy eventually leads to heart failure without adequate treatment. The immunoproteasome is an inducible form of the proteasome that is intimately involved in inflammatory diseases. Here, we found that the expression and activity of immunoproteasome catalytic subunit ?5i were significantly up-regulated in angiotensin II (Ang II)-treated cardiomyocytes and in the hypertrophic hearts. Knockout of ?5i in cardiomyocytes and mice markedly attenuated the hypertrophic response, and this effect was aggravated by ?5i overexpression in cardiomyocytes and transgenic mice. Mechanistically, ?5i interacted with and promoted ATG5 degradation thereby leading to inhibition of autophagy and cardiac hypertrophy. Further, knockdown of ATG5 or inhibition of autophagy reversed the ?5i knockout-mediated reduction of cardiomyocyte hypertrophy induced by Ang II or pressure overload. Together, this study identifies a novel role for ?5i in the regulation of cardiac hypertrophy. The inhibition of ?5i activity may provide a new therapeutic approach for hypertrophic diseases.

SUBMITTER: Xie X 

PROVIDER: S-EPMC6506244 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature