Journal
MEDCOMM
Volume 2, Issue 1, Pages 91-100Publisher
WILEY
DOI: 10.1002/mco2.58
Keywords
autophagy; hepatic ischemia-reperfusion injury; IRF-1; JNK
Categories
Funding
- NationalNatural Science Foundation of China [81700556]
- Henan Medical Science andTechnology Program [SB201902007]
- Colleges and Universities in Henan Province [20A320077]
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The study shows that IRF-1 is upregulated in response to hepatic ischemia-reperfusion injury and is associated with autophagic activation, leading to aggravated liver damage. The effects of IRF-1 are linked to JNK pathway activation and increased Beclin1 protein levels, resulting in JNK-induced autophagic cell death and cell failure. These findings suggest that the IRF-1/JNK pathway activates autophagy to worsen liver IRI and may offer new insights into protective therapies.
Increasing evidence has accrued indicating that autophagy is associated with hepatic ischemia-reperfusion injury (IRI). This report demonstrates that interferon regulatory factor-1 (IRF-1) was upregulated in response to hepatic IRI and was associated with autophagic activation. As a result of these processes, there is an aggravation of liver damage, effects that can be offset by IRF-1 depletion. In addition, these effects of IRF-1 are associated with JNK pathway activation followed by increases in Beclin1 protein levels. This JNK-induced autophagic cell death then leads to cell failure, and plays an important role in liver function damage. We conclude that IRF-1 activates autophagy through JNK-mediated autophagy. Accordingly, these findings indicating that the IRF-1/JNK pathway activates autophagy to exacerbate liver IRI in this mouse model may provide new insights into novel protective therapies for hepatic IRI.
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