LncRNA 0003250 accelerates heart autophagy and binds to miR-17-5p as a competitive endogenous RNA in chicken induced by selenium deficiency

J Cell Physiol. 2021 Jan;236(1):157-177. doi: 10.1002/jcp.29831. Epub 2020 Jun 15.

Abstract

Long noncoding RNAs (LncRNAs) have been demonstrated to be associated with a variety of myocardial diseases, but how LncRNAs regulate autophagy in selenium (Se)-deficient myocardial injury is infrequently reported. Here, we screened out a novel long noncoding RNA, microRNA, and ATG7 through transcriptomic results. We employed a Se-deficient chicken model in vivo, and primary cultured cardiomyocytes treated by correlation in vitro. The results showed that Se deficiency upregulated the expression of ATG7, and miR-17-5p inhibited cardiomyocyte autophagy by targeting ATG7. Furthermore, we found that LncRNA 0003250 regulated miR-17-5p, and thus affected the expression of ATG7 and autophagic cell death. Our present study proposed a novel model for the regulation of cardiomyocytes autophagy, which includes LncRNA 0003250, miR-17-5p and ATG7 in the chicken heart. Our conclusions may provide a feasible diagnostic tool for Se-deficient cardiomyocyte injury.

Keywords: autophagy; ceRNA; chicken heart; selenium deficiency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy / genetics*
  • Chickens / genetics*
  • Heart / physiopathology*
  • MicroRNAs / genetics*
  • Myocytes, Cardiac / pathology
  • RNA, Long Noncoding / genetics*
  • Selenium / deficiency*
  • Transcriptome / genetics
  • Up-Regulation / genetics

Substances

  • MicroRNAs
  • RNA, Long Noncoding
  • Selenium