Selective Autophagy Receptors in Antiviral Defense

被引:30
作者
Viret, Christophe [1 ]
Duclaux-Loras, Remi [1 ,2 ]
Nancey, Stephane [1 ,3 ]
Rozieres, Aurore [1 ]
Faure, Mathias [1 ,4 ]
机构
[1] Univ Claude Bernard Lyon 1, Univ Lyon, CNRS,Ctr Int Rech Infectiol,ENS Lyon,CIRI, INSERM,Team Autophagy Infect Immun,U1111,UMR5308, F-69007 Lyon, France
[2] Hosp Civils Lyon, Femme Mere Enfant Hosp, Dept Pediat Hepatol Gastroenterol & Nutr, Bron, France
[3] Hosp Civils Lyon, Lyon Sud Hosp, Dept Gastroenterol, Lyon, France
[4] Equipe Labellisee Fondat Rech Med, FRM, Paris, France
关键词
VIRUS-INDUCED AUTOPHAGY; DROSOPHILA-MELANOGASTER; IMMUNE-RESPONSE; INNATE; PROTEIN; DEGRADATION; UBIQUITIN; INFECTION; KINASE; REPLICATION;
D O I
10.1016/j.tim.2021.02.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autophagy ensures the degradation of cytosolic substrates by the lysosomal pathway. Cargoes destined to be eliminated are confined within double membrane vesicles called autophagosomes, prior to fusion with endolysosomal vacuoles. Autophagy receptors selectively interact with cargoes and route them to elongating autophagic membranes, a process referred to as selective autophagy. Besides contributing to cell homeostasis, selective autophagy constitutes an important cell-autonomous defense mechanism against viruses. We review observations related to selective autophagy receptor engagement during host cell responses to virus infection. We examine the distinct roles of autophagy receptors in antiviral autophagy, consider the strategies viruses have evolved to escape or oppose such restrictions, and delineate the contributions of selective autophagy to the tailoring of antiviral innate responses. Finally, we mention some open and emerging questions in the field.
引用
收藏
页码:798 / 810
页数:13
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