作者
Omar Motiño, Flavia Lambertucci, Gerasimos Anagnostopoulos, Sijing Li, Jihoon Nah, Francesca Castoldi, Laura Senovilla, Léa Montégut, Hui Chen, Sylvère Durand, Mélanie Bourgin, Fanny Aprahamian, Nitharsshini Nirmalathasan, Karla Alvarez-Valadez, Allan Sauvat, Vincent Carbonnier, Mojgan Djavaheri-Mergny, Federico Pietrocola, Junichi Sadoshima, Maria Chiara Maiuri, Isabelle Martins, Guido Kroemer
发表日期
2022/10/11
期刊
Proceedings of the National Academy of Sciences
卷号
119
期号
41
页码范围
e2207344119
出版商
National Academy of Sciences
简介
Acyl-coenzyme A (CoA)–binding protein (ACBP), also known as diazepam-binding inhibitor (DBI), is an extracellular feedback regulator of autophagy. Here, we report that injection of a monoclonal antibody neutralizing ACBP/DBI (α-DBI) protects the murine liver against ischemia/reperfusion damage, intoxication by acetaminophen and concanavalin A, and nonalcoholic steatohepatitis caused by methionine/choline-deficient diet as well as against liver fibrosis induced by bile duct ligation or carbon tetrachloride. α-DBI downregulated proinflammatory and profibrotic genes and upregulated antioxidant defenses and fatty acid oxidation in the liver. The hepatoprotective effects of α-DBI were mimicked by the induction of ACBP/DBI-specific autoantibodies, an inducible Acbp/Dbi knockout or a constitutive Gabrg2F77I mutation that abolishes ACBP/DBI binding to the GABAA receptor. Liver-protective α-DBI effects were lost …
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