Targeting APT2 improves MAVS palmitoylation and antiviral innate immunity.

Autor:	Bu L; Center of Lung Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China. Electronic address: bulang@mail3.sysu.edu.cn., Wang H; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Zhang S; Center of Lung Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Zhang Y; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Liu M; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Zhang Z; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Wu X; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Jiang Q; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Wang L; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Xie W; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China., He M; Centre for Infection and Immunity Study (CIIS), School of Medicine (Shenzhen), Sun Yat-sen University, Guangzhou, Guangdong 510275, China., Zhou Z; Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, Guangdong 510275, China., Cheng C; Center of Lung Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China. Electronic address: chengch3@mail.sysu.edu.cn., Guo J; Institute of Precision Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510275, China. Electronic address: guojp6@mail.sysu.edu.cn.
Jazyk:	angličtina
Zdroj:	Molecular cell [Mol Cell] 2024 Sep 19; Vol. 84 (18), pp. 3513-3529.e5. Date of Electronic Publication: 2024 Sep 09.
DOI:	10.1016/j.molcel.2024.08.014
Abstrakt:	Innate immunity serves as the primary defense against viral and microbial infections in humans. The precise influence of cellular metabolites, especially fatty acids, on antiviral innate immunity remains largely elusive. Here, through screening a metabolite library, palmitic acid (PA) has been identified as a key modulator of antiviral infections in human cells. Mechanistically, PA induces mitochondrial antiviral signaling protein (MAVS) palmitoylation, aggregation, and subsequent activation, thereby enhancing the innate immune response. The palmitoyl-transferase ZDHHC24 catalyzes MAVS palmitoylation, thereby boosting the TBK1-IRF3-interferon (IFN) pathway, particularly under conditions of PA stimulation or high-fat-diet-fed mouse models, leading to antiviral immune responses. Additionally, APT2 de-palmitoylates MAVS, thus inhibiting antiviral signaling, suggesting that its inhibitors, such as ML349, effectively reverse MAVS activation in response to antiviral infections. These findings underscore the critical role of PA in regulating antiviral innate immunity through MAVS palmitoylation and provide strategies for enhancing PA intake or targeting APT2 for combating viral infections. Competing Interests: Declaration of interests The authors declare no competing interests. (Copyright © 2024 Elsevier Inc. All rights reserved.)
Databáze:	MEDLINE
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