抗菌肽
先天免疫系统
免疫系统
生物
细胞生物学
效应器
附带损害
细胞毒性
抗菌剂
细胞毒性T细胞
微生物学
免疫学
体外
生物化学
犯罪学
社会学
作者
Samuel Rommelaere,Alexia Carboni,Juan F. Bada Juarez,Jean-Philippe Boquete,Luciano A. Abriata,Fernando Teixeira Pinto Meireles,Verena Rukes,Crystal M. Vincent,Shu Kondo,Marc Dionne,Matteo Dal Peraro,Chan Cao,Bruno Lemaître
出处
期刊:Current Biology
[Elsevier]
日期:2024-03-13
卷期号:34 (7): 1426-1437.e6
被引量:2
标识
DOI:10.1016/j.cub.2024.02.049
摘要
7An efficient immune system must provide protection against a broad range of pathogens without causing excessive collateral tissue damage. While immune effectors have been well characterized, we know less about the resilience mechanisms protecting the host from its own immune response. Antimicrobial peptides (AMPs) are small, cationic peptides that contribute to innate defenses by targeting negatively charged membranes of microbes. While protective against pathogens, AMPs can be cytotoxic to host cells. Here, we reveal that a family of stress-induced proteins, the Turandots, protect the Drosophila respiratory system from AMPs, increasing resilience to stress. Flies lacking Turandot genes are susceptible to environmental stresses due to AMP-induced tracheal apoptosis. Turandot proteins bind to host cell membranes and mask negatively charged phospholipids, protecting them from cationic pore-forming AMPs. Collectively, these data demonstrate that Turandot stress proteins mitigate AMP cytotoxicity to host tissues and therefore improve their efficacy.
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