Function of autophagy genes in innate immune defense against mucosal pathogens

被引:0
|
作者
Cui, Xiaoyan [1 ]
Wang, Ya-Ting [1 ,2 ]
机构
[1] Tsinghua Univ, Ctr Infect Dis Res, Sch Basic Med Sci, Beijing 100084, Peoples R China
[2] Shanxi Med Univ, SXMU Tsinghua Collaborat Innovat Ctr Frontier Med, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
MYCOBACTERIUM-TUBERCULOSIS; SELECTIVE AUTOPHAGY; LUNG INFLAMMATION; MATRIX PROTEIN-2; CELL AUTOPHAGY; INFECTION; DISEASE; ATG16L1; SURVIVAL; COMPLEX;
D O I
10.1016/j.mib.2024.102456
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mucosal immunity is posed to constantly interact with commensal microbes and invading pathogens. As a fundamental cell biological pathway affecting immune response, autophagy regulates the interaction between mucosal immunity and microbes through multiple mechanisms, including direct elimination of microbes, control of inflammation, antigen presentation and lymphocyte homeostasis, and secretion of immune mediators. Some of these physiologically important functions do not involve canonical degradative autophagy but rely on certain autophagy genes and their 'autophagy gene-specific functions.' Here, we review the relationship between autophagy and important mucosal pathogens, including influenza virus, Mycobacterium tuberculosis, Salmonella enterica, Citrobacter rodentium, norovirus, and herpes simplex virus, with a particular focus on distinguishing the canonical versus gene-specific mechanisms of autophagy genes.
引用
收藏
页数:13
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