效应器
细胞生物学
内体
ESCRT公司
生物
上睑下垂
程序性细胞死亡
泛素
泛素连接酶
排序nexin
细胞凋亡
细胞内
生物化学
基因
作者
Caroline Stefani,Anna M. Bruchez,Mario G. Rosasco,A Yoshida,Kayla J. Fasano,Paula F. Levan,Alina Lorant,Nicholas Hubbard,Andrew Oberst,Lynda M. Stuart,Adam Lacy‐Hulbert
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2024-01-05
卷期号:9 (91)
被引量:2
标识
DOI:10.1126/sciimmunol.abq6541
摘要
Pore-forming toxins (PFTs) are the largest class of bacterial toxins and contribute to virulence by triggering host cell death. Vertebrates also express endogenous pore-forming proteins that induce cell death as part of host defense. To mitigate damage and promote survival, cells mobilize membrane repair mechanisms to neutralize and counteract pores, but how these pathways are activated is poorly understood. Here, we use a transposon-based gene activation screen to discover pathways that counteract the cytotoxicity of the archetypal PFT
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