{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Tong G"],"funding":["National Natural Science Foundation of China"],"pagination":["6107"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10542385"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["14(1)"],"pubmed_abstract":["Hepatic ischemia-reperfusion injury (IRI) is a common complication occurs during hepatic resection and transplantation. However, the mechanisms underlying hepatic IRI have not been fully elucidated. Here, we aim to explore the role of fibroblast growth factor 18 (FGF18) in hepatic IRI. In this work, we find that Hepatic stellate cells (HSCs) secrete FGF18 and alleviates hepatocytes injury. HSCs-specific FGF18 deletion largely aggravates hepatic IRI. Mechanistically, FGF18 treatment reduces the levels of ubiquitin carboxyl-terminal hydrolase 16 (USP16), leading to increased ubiquitination levels of Kelch Like ECH Associated Protein 1 (KEAP1) and the activation of nuclear factor erythroid 2-related factor 2 (Nrf2). Furthermore, USP16 interacts and deubiquitinates KEAP1. More importantly, Nrf"],"journal":["Nature communications"],"pubmed_title":["FGF18 alleviates hepatic ischemia-reperfusion injury via the USP16-mediated KEAP1/Nrf2 signaling pathway in male mice."],"pmcid":["PMC10542385"],"funding_grant_id":["82070507"],"pubmed_authors":["Shen J","Hu Z","Chen H","Wu Z","Li X","Li S","Zhu J","Feng J","Fan J","Zhu K","Zhou B","Cong W","Chen Y","Chen X","Tong G","Jin L"],"additional_accession":[]},"is_claimable":false,"name":"FGF18 alleviates hepatic ischemia-reperfusion injury via the USP16-mediated KEAP1/Nrf2 signaling pathway in male mice.","description":"Hepatic ischemia-reperfusion injury (IRI) is a common complication occurs during hepatic resection and transplantation. However, the mechanisms underlying hepatic IRI have not been fully elucidated. Here, we aim to explore the role of fibroblast growth factor 18 (FGF18) in hepatic IRI. In this work, we find that Hepatic stellate cells (HSCs) secrete FGF18 and alleviates hepatocytes injury. HSCs-specific FGF18 deletion largely aggravates hepatic IRI. Mechanistically, FGF18 treatment reduces the levels of ubiquitin carboxyl-terminal hydrolase 16 (USP16), leading to increased ubiquitination levels of Kelch Like ECH Associated Protein 1 (KEAP1) and the activation of nuclear factor erythroid 2-related factor 2 (Nrf2). Furthermore, USP16 interacts and deubiquitinates KEAP1. More importantly, Nrf","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Sep","modification":"2025-07-09T03:04:57.112Z","creation":"2025-02-18T23:59:18.552Z"},"accession":"S-EPMC10542385","cross_references":{"pubmed":["37777507"],"doi":["10.1038/s41467-023-41800-x"]}}