MHC I级
细胞生物学
MHC II级
生物
CD8型
主要组织相容性复合体
T细胞
细胞毒性T细胞
树突状细胞
免疫学
病毒学
免疫系统
遗传学
体外
作者
Monica Loi,Anne Müller,Karin Steinbach,Jennifer Niven,Rosa Barreira da Silva,Petra Paul,Laure‐Anne Ligeon,Assunta Caruso,Randy A. Albrecht,Andrea C. Becker,Nicolas Annaheim,Heike Nowag,Jörn Dengjel,Adolfo García‐Sastre,Doron Merkler,Christian Münz,Monique Gannagé
出处
期刊:Cell Reports
[Cell Press]
日期:2016-04-30
卷期号:15 (5): 1076-1087
被引量:165
标识
DOI:10.1016/j.celrep.2016.04.002
摘要
The macroautophagy machinery has been implicated in MHC class II restricted antigen presentation. Here, we report that this machinery assists in the internalization of MHC class I molecules. In the absence of the autophagy factors Atg5 and Atg7, MHC class I surface levels are elevated due to decreased endocytosis and degradation. Internalization of MHC class I molecules occurs less efficiently if AAK1 cannot be recruited via Atg8/LC3B. In the absence of Atg-dependent MHC class I internalization, dendritic cells stimulate CD8(+) T cell responses more efficiently in vitro and in vivo. During viral infections, lack of Atg5 results in enhanced influenza- and LCMV-specific CD8(+) T cell responses in vivo. Elevated influenza-specific CD8(+) T cell responses are associated with better immune control of this infection. Thus, the macroautophagy machinery orchestrates T cell immunity by supporting MHC class II but compromises MHC class I restricted antigen presentation.
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