Long Noncoding RNA AK12348 is Involved in the Regulation of Myocardial Ischaemia-Reperfusion Injury by Targeting PARP and Caspase-3

Heart Lung Circ. 2018 May;27(5):e51-e58. doi: 10.1016/j.hlc.2017.04.011. Epub 2017 May 26.

Abstract

Backgroud: Recently long non-coding RNAs (lncRNAs) have attracted attention in several biomedical fields. The purpose of this study is to investigate the profile of myocardial lncRNAs and their potential roles in myocardial ischaemia-reperfusion injury (IRI).

Methods: EdgeR bioconductor package was used to screen differentially expressed lncRNAs in myocardial IRI, and lncRNA AK12348 was selected. The mRNA levels of lncRNA AK12348 in normal and anoxia/reoxygenation (A/R) cardiomyocytes were determined by qRT-PCR. After transfection with siRNA-lncRNA, AK12348, LDH release and cell apoptotic rates in normal and A/R cardiomyocytes were determined. The protein expression values of PARP and Caspase-3 were also determined by western blotting.

Results: The relative level of lncRNA AK12348, LDH release and cell apoptotic rate in A/R cardiomyocytes was significantly higher than that in normal cardiomyocytes. After transfection with siRNA-lncRNA AK12348, LDH release and cell apoptotic rates in A/R cardiomyocytes were reduced, while the values in normal cardiomyocytes had almost no change. The protein expression values of PARP and Caspase-3 in A/R cardiomyocytes were much higher than the Control. After knockdown of lncRNA AK12348, the values decreased.

Conclusion: Long non-coding RNAs AK12348 could be potential therapeutic targets for the treatment of myocardial IRI.

Keywords: A/R; LDH; LncRNA AK12348; Myocardial IRI; PARP.

MeSH terms

  • Animals
  • Apoptosis
  • Blotting, Western
  • Caspase 3 / biosynthesis
  • Caspase 3 / genetics*
  • Disease Models, Animal
  • Flow Cytometry
  • Gene Expression Regulation*
  • Immunohistochemistry
  • Myocardial Reperfusion Injury / genetics*
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / pathology
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / pathology
  • Poly(ADP-ribose) Polymerases / biosynthesis
  • Poly(ADP-ribose) Polymerases / genetics*
  • RNA, Long Noncoding / genetics*
  • RNA, Messenger / genetics*
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction

Substances

  • RNA, Long Noncoding
  • RNA, Messenger
  • Poly(ADP-ribose) Polymerases
  • Caspase 3