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作 者:Jing Wang Richard A. Flavell Hua-Bing Li
机构地区:[1]Shanghai Institute of Immunology, Key Laboratory of Cell Differentiation and Apoptosis of Ministry of Education of China, Shanghai Jiao Tong University School of Medicine, 200025 Shanghai, China [2]Yale Center for ImmunoMetabolism, Shanghai Jiao Tong University School of Medicine, 200025 Shanghai, China [3]Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520-8055, USA [4]Howard Hughes Medical Institute, Yale University, New Haven, CT 06520-8055, USA
出 处:《Cell Research》2019年第3期177-178,共2页细胞研究(英文版)
基 金:National Natural Science Foundation of China (91753141 to HBL).
摘 要:A recent study in Cell Research by Hu et al. describes a novel function of intracellular bile acids (BAs), a class of cholesterolderived metabolites, which activate several key innate antiviral signaling components through the TGR5-p-arrestin- SRC pathway to potentiate antiviral immunity. This finding adds a new metabolic regulatory dimension of innate antiviral response and provides a new antiviral strategy by supplementing BAs.
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