MiR-132 Regulates Rem Expression in Cardiomyocytes During Long-Term β-Adrenoceptor Agonism

Cell Physiol Biochem. 2015;36(1):141-54. doi: 10.1159/000374059. Epub 2015 Apr 30.

Abstract

Aims: To characterize the effects of long-term β-adrenergic receptor stimulation on Rem protein and mRNA expression in rat heart and possible involvement of miR-132.

Methods: Adult rats were treated with isoproterenol (ISO, 150 µg.kg.h(-1)) for 2 d and Rem, miR-132, and α1c (the principal subunit of Cav1.2 channels) were measured at protein and mRNA levels with western blot and quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) experiments, respectively. Ca(2+) currents and intracellular Ca(2+) signals were evaluated in isolated cardiomyocytes.

Results: Systemic administration of ISO led to decreases in Rem protein and mRNA levels (down to 49%). Furthermore, levels of the microRNAs (miRs) miR-132 and miR-214 were upregulated 5- and 9-fold, respectively. Transfection of miR-132, but not miR-214, into HEK293 cells reduced the expression of a luciferase reporter gene controlled by a conserved 3´-untranslated region (UTR) of Rem by half. Chronic ISO administration also led to a 25% decrease in the amplitude of peak L-type Ca(2+) currents, a 40% decrease in α1c subunit protein abundance at the membrane level, and a 60% decrease in expression of α1c channel subunit mRNA.

Conclusions: These results suggest that Rem expression is down-regulated posttranscriptionally by miR-132 in response to long-term activation of β-adrenergic signaling, but this down-regulation does not produce a larger Ca(2+) influx through Cav1.2 channels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / drug effects
  • Adrenergic beta-Agonists / administration & dosage*
  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Calcium / metabolism
  • Gene Expression Regulation / drug effects
  • HEK293 Cells
  • Humans
  • Isoproterenol / administration & dosage*
  • Isoproterenol / pharmacology
  • Male
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Monomeric GTP-Binding Proteins / genetics*
  • Monomeric GTP-Binding Proteins / metabolism
  • Myocytes, Cardiac / drug effects*
  • Myocytes, Cardiac / metabolism
  • Rats
  • Rats, Wistar

Substances

  • 3' Untranslated Regions
  • Adrenergic beta-Agonists
  • MIRN124 microRNA, rat
  • MIRN132 microRNA, rat
  • MicroRNAs
  • Rem protein, mouse
  • Monomeric GTP-Binding Proteins
  • Isoproterenol
  • Calcium