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• W3119192004 endingPage "101859" @default.
• W3119192004 startingPage "101859" @default.
• W3119192004 abstract "Hepatic ischemia-reperfusion injury (IRI) is a major complication of liver surgery and transplantation. IRI leads to hepatic parenchymal cell death, resulting in liver failure, and lacks effective therapeutic approaches. Fibroblast growth factor 10 (FGF10) is a paracrine factor which is well-characterized with respect to its pro-proliferative effects during embryonic liver development and liver regeneration, but its role in hepatic IRI remains unknown. In this study, we investigated the role of FGF10 in liver IRI and identified signaling pathways regulated by FGF10. In a mouse model of warm liver IRI, FGF10 was highly expressed during the reperfusion phase. In vitro experiments demonstrated that FGF10 was primarily secreted by hepatic stellate cells and acted on hepatocytes. The role of FGF10 in liver IRI was further examined using adeno-associated virus-mediated gene silencing and overexpression. Overexpression of FGF10 alleviated liver dysfunction, reduced necrosis and inflammation, and protected hepatocytes from apoptosis in the early acute injury phase of IRI. Furthermore, in the late phase of IRI, FGF10 overexpression also promoted hepatocyte proliferation. Meanwhile, gene silencing of FGF10 had the opposite effect. Further studies revealed that overexpression of FGF10 activated nuclear factor-erythroid 2-related factor 2 (NRF2) and decreased oxidative stress, mainly through activation of the phosphatidylinositol-3-kinase/AKT pathway, and the protective effects of FGF10 overexpression were largely abrogated in NRF2 knockout mice. These results demonstrate the protective effects of FGF10 in liver IRI, and reveal the important role of NRF2 in FGF10-mediated hepatic protection during IRI. • FGF10 is markedly upregulated in the early phase of liver IRI. • FGF10 overexpression exerts great potential in ameliorating hepatic IRI. • FGF10 knockdown significantly aggravates hepatic IRI. • FGF10 overexpression activates PI3K/AKT-NRF2 signaling and thus ameliorates hepatic IRI. • NRF2 knockout abrogates the protective effects of FGF10 overexpression during liver IRI." @default.
• W3119192004 created "2021-01-18" @default.
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• W3119192004 date "2021-04-01" @default.
• W3119192004 modified "2023-10-07" @default.
• W3119192004 title "The protective effects of fibroblast growth factor 10 against hepatic ischemia-reperfusion injury in mice" @default.
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• W3119192004 doi "https://doi.org/10.1016/j.redox.2021.101859" @default.
• W3119192004 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7806526" @default.
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• W3119192004 hasPublicationYear "2021" @default.
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