Nuclear receptor subfamily 4 group A member 1 promotes myocardial ischemia/reperfusion injury through inducing mitochondrial fission factor-mediated mitochondrial fragmentation and inhibiting FUN14 domain containing 1-depedent mitophagy

Guangzhou University of Chinese Medicine · The 309th Hospital of Chinese People's Liberation Army · +3 more institutions

PubMed
Indexed incrossrefdoajpubmed

Abstract

This study investigated the mechanism by which NR4A1 regulates mitochondrial fission factor (Mff)-related mitochondrial fission and FUN14 domain 1 (FUNDC1)-mediated mitophagy following cardiac ischemia-reperfusion injury(I/R). Our findings showed that the damage regulation was positively correlated with the pathological fission and pan-apoptosis of myocardial cell mitochondria. Compared with wild-type mice (WT), NR4A1-knockout mice exhibited resistance to myocardial ischemia-reperfusion injury and mitochondrial pathological fission, characterized by mitophagy activation. Results showed that ischemia-reperfusion injury increased NR4A1 expression level, activating mitochondrial fission mediated by Mff and…

Citation impact

159
total citations
FWCI
57.43
Percentile
100%
References
66
Citations per year

Authors

11

Topics & keywords

Keywords
  • Mitophagy
  • Mitochondrial fission
  • Subfamily
  • Biology
  • Fragmentation (computing)
  • Reperfusion injury
  • Mitochondrion
  • Cell biology
UN Sustainable Development Goals
  • Good health and well-being
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