Mir-24 regulates junctophilin-2 expression in cardiomyocytes

Circ Res. 2012 Sep 14;111(7):837-41. doi: 10.1161/CIRCRESAHA.112.277418. Epub 2012 Aug 13.

Abstract

Rationale: Failing cardiomyocytes exhibit decreased efficiency of excitation-contraction (E-C) coupling. The downregulation of junctophilin-2 (JP2), a protein anchoring the sarcoplasmic reticulum to T-tubules, has been identified as a major mechanism underlying the defective E-C coupling. However, the regulatory mechanism of JP2 remains unknown.

Objective: To determine whether microRNAs regulate JP2 expression.

Methods and results: Bioinformatic analysis predicted 2 potential binding sites of miR-24 in the 3'-untranslated regions of JP2 mRNA. Luciferase assays confirmed that miR-24 suppressed JP2 expression by binding to either of these sites. In the aortic stenosis model, miR-24 was upregulated in failing cardiomyocytes. Adenovirus-directed overexpression of miR-24 in cardiomyocytes decreased JP2 expression and reduced Ca(2+) transient amplitude and E-C coupling gain.

Conclusions: MiR-24-mediated suppression of JP2 expression provides a novel molecular mechanism for E-C coupling regulation in heart cells and suggests a new target against heart failure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aortic Valve Stenosis / metabolism*
  • Aortic Valve Stenosis / pathology
  • Calcium / metabolism
  • Cells, Cultured
  • Computational Biology
  • Excitation Contraction Coupling / physiology
  • Heart Failure / metabolism*
  • Heart Failure / pathology
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Models, Animal
  • Myocytes, Cardiac / metabolism*
  • Myocytes, Cardiac / pathology
  • RNA, Messenger / metabolism
  • Rats
  • Sarcoplasmic Reticulum / physiology
  • Up-Regulation*

Substances

  • MIRN24 microRNA, rat
  • Membrane Proteins
  • MicroRNAs
  • RNA, Messenger
  • junctophilin
  • Calcium