microRNA-183 Mediates Protective Postconditioning of the Liver by Repressing Apaf-1

Antioxid Redox Signal. 2017 Apr 10;26(11):583-597. doi: 10.1089/ars.2016.6679. Epub 2016 Nov 2.

Abstract

Aims: Ischemic postconditioning (iPoC) is known to mitigate ischemia-reperfusion (IR) injury of the liver, the mechanisms of which remain to be elucidated. This study explored the role of microRNA-183 (miR-183) in the protective mechanism of iPoC.

Results: Microarray analysis showed miR-183 was robustly expressed in rats' livers with iPoC. miR-183 repressed the mRNA expression of Apaf-1, which is an apoptosis promoting factor. Using an oxygen-glucose deprivation (OGD) injury model in Clone 9 cells, hypoxic postconditioning (HPoC) and an miR-183 mimetic significantly decreased cell death after OGD, but miR-183 inhibitors eliminated the protection of HPoC. The increased expression of Apaf-1 and the downstream activation of capsase-3/9 after OGD were mitigated by HPoC or the addition of miR-183 mimetics, whereas miR-183 inhibitor diminished the effect of HPoC on Apaf-1-caspase signaling. In the in vivo experiment, iPoC and agomiR-183 decreased the expression of serum ALT after liver IR in the mice, but antagomiR-183 mitigated the effect of iPoC. The results of hematoxylin and eosin and TUNEL staining were compatible with the biochemical assay. Moreover, iPoC and agomiR-183 decreased the expression of Apaf-1 and 4-HNE after IR injury in mouse livers, whereas the antagomiR-mediated prevention of miR-183 expression led to increased protein expression of Apaf-1 and 4-HNE in the postischemic livers.

Innovation: Our experiment showed the first time that miR-183 was induced in protective postconditioning and reduced reperfusion injury of the livers via the targeting of apoptotic signaling.

Conclusion: miR-183 mediated the tolerance induced by iPoC in livers via Apaf-1 repressing. Antioxid. Redox Signal. 26, 583-597.

Keywords: hypoxic postconditioning; miR-183; oxygen-glucose deprivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Apoptotic Protease-Activating Factor 1 / genetics*
  • Gene Expression
  • Gene Expression Regulation
  • Glucose / metabolism
  • Ischemic Postconditioning*
  • Liver / blood supply*
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Mice
  • MicroRNAs / genetics*
  • Oxidative Stress
  • Oxygen / metabolism
  • RNA Interference*
  • Rats
  • Reperfusion Injury / genetics
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / pathology
  • Signal Transduction

Substances

  • Apoptotic Protease-Activating Factor 1
  • MIRN183 microRNA, rat
  • MicroRNAs
  • Mirn183 microRNA, mouse
  • Glucose
  • Oxygen