miR-30a downregulation aggravates pressure overload-induced cardiomyocyte hypertrophy

Mol Cell Biochem. 2013 Jul;379(1-2):1-6. doi: 10.1007/s11010-012-1552-z. Epub 2013 May 10.

Abstract

miRNAs play an important role in the pathogenesis of cardiac hypertrophy and dysfunction. However, little is known about how miR-30a regulates cardiomyocyte hypertrophy. In the study, Male C57BL/6 mice were subjected to thoracic aortic constriction, and hearts were harvested at 3 weeks. We assayed miR-30a expression level by real-time PCR and defined the molecular mechanisms of miR-30a-mediated cardiomyocyte hypertrophy. We found that myocardial expression of miR-30a was decreased in mouse models of hypertrophy and in H9c2 cells treated with phenylephrine. MiR-30a inhibition markedly increased mRNA expression of cardiac hypertrophy markers such as atrial natriuretic factor and brain natriuretic peptide in H9c2, and cell size was increased after miR-30a inhibitor treatment. Downregulated miR-30a activated autophagy by inhibiting beclin-1 expression in H9c2 cell. More important, autophagy inhibition suppressed miR-30a inhibitor-induced cardiomyocyte hypertrophy. Together, our data demonstrated that downregulated miR-30a aggravates pressure overload-induced cardiomyocyte hypertrophy by activating autophagy, thus offering a new target for the therapy of cardiomyocyte hypertrophy.

MeSH terms

  • 3' Untranslated Regions
  • Animals
  • Atrial Natriuretic Factor / genetics
  • Atrial Natriuretic Factor / metabolism
  • Autophagy
  • Cardiomegaly / etiology
  • Cardiomegaly / metabolism*
  • Cardiomegaly / pathology
  • Cell Line
  • Cell Size
  • Down-Regulation
  • Gene Expression Regulation
  • HEK293 Cells
  • Humans
  • Hypertension / complications
  • Hypertension / metabolism*
  • Hypertension / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Myocardium / metabolism
  • Myocardium / pathology
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / pathology
  • Natriuretic Peptide, Brain / genetics
  • Natriuretic Peptide, Brain / metabolism
  • Rats

Substances

  • 3' Untranslated Regions
  • MicroRNAs
  • Mirn30d microRNA, mouse
  • Natriuretic Peptide, Brain
  • Atrial Natriuretic Factor