| Literature DB >> 27117419 |
Monica Loi1, Anne Müller1, Karin Steinbach2, Jennifer Niven3, Rosa Barreira da Silva1, Petra Paul1, Laure-Anne Ligeon1, Assunta Caruso3, Randy A Albrecht4, Andrea C Becker5, Nicolas Annaheim1, Heike Nowag1, Jörn Dengjel5, Adolfo García-Sastre6, Doron Merkler7, Christian Münz8, Monique Gannagé9.
Abstract
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.Entities:
Keywords: AAK1; LCMV; endocytosis; immune control; influenza
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Year: 2016 PMID: 27117419 DOI: 10.1016/j.celrep.2016.04.002
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423