Autophagy promotes MHC class II presentation of peptides from intracellular source proteins

被引:503
作者
Dengjel, J
Schoor, O
Fischer, R
Reich, M
Kraus, M
Müller, M
Kreymborg, K
Altenberend, F
Brandenburg, J
Kalbacher, H
Brock, R
Driessen, C
Rammensee, HG
Stevanovic, S [1 ]
机构
[1] Univ Tubingen, Dept Immunol, D-72076 Tubingen, Germany
[2] Univ Tubingen, Dept Biol Mol, Inst Cell Biol, D-72076 Tubingen, Germany
[3] Univ Tubingen, Dept Med 2, D-72076 Tubingen, Germany
[4] Univ Tubingen, Med & Nat Sci Res Ctr, D-72076 Tubingen, Germany
关键词
antigen processing; lysosomal proteases; T helper cells;
D O I
10.1073/pnas.0501190102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MHC-peptide complexes mediate key functions in adaptive immunity. in a classical view, MHC-I molecules present peptides from intracellular source proteins, whereas MHC-II molecules present antigenic peptides from exogenous and membrane proteins. Nevertheless, substantial crosstalk between these two pathways has been observed. We investigated the influence of autophagy on the MHC-II ligandome and demonstrated that peptide presentation is altered considerably upon induction of autophagy. The presentation of peptides from intracellular and lysosomal source proteins was strongly increased on MHC-II in contrast with peptides from membrane and secreted proteins. In addition, autophagy influenced the MHC-II antigen-processing machinery. Our study illustrates a profound influence of autophagy on the class II peptide repertoire and suggests that this finding has implications for the regulation of CD4(+) T cell-mediated processes.
引用
收藏
页码:7922 / 7927
页数:6
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