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

被引:500
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
相关论文
共 46 条
  • [1] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [2] Beck H, 2001, EUR J IMMUNOL, V31, P3726, DOI 10.1002/1521-4141(200112)31:12<3726::AID-IMMU3726>3.0.CO
  • [3] 2-O
  • [4] BIEDERBICK A, 1995, EUR J CELL BIOL, V66, P3
  • [5] Cathepsin G, and not the asparagine-specific endoprotease, controls the processing of myelin basic protein in lysosomes from human B lymphocytes
    Burster, T
    Beck, A
    Tolosa, E
    Marin-Esteban, V
    Rötzschke, O
    Falk, K
    Lautwein, A
    Reich, M
    Brandenburg, J
    Schwarz, G
    Wiendl, H
    Melms, A
    Lehmann, R
    Stevanovic, S
    Kalbacher, H
    Driessen, C
    [J]. JOURNAL OF IMMUNOLOGY, 2004, 172 (09) : 5495 - 5503
  • [6] SPECIFICITY AND PROMISCUITY AMONG NATURALLY PROCESSED PEPTIDES BOUND TO HLA-DR ALLELES
    CHICZ, RM
    URBAN, RG
    GORGA, JC
    VIGNALI, DAA
    LANE, WS
    STROMINGER, JL
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (01) : 27 - 47
  • [7] Differential lysosomal proteolysis in antigen-presenting CeRs determines antigen fate
    Delamarre, L
    Pack, M
    Chang, H
    Mellman, I
    Trombetta, ES
    [J]. SCIENCE, 2005, 307 (5715) : 1630 - 1634
  • [8] Glycan side chains on naturally presented MHC class II ligands
    Dengjel, J
    Rammensee, HG
    Stevanovic, S
    [J]. JOURNAL OF MASS SPECTROMETRY, 2005, 40 (01): : 100 - 104
  • [9] DAVID: Database for annotation, visualization, and integrated discovery
    Dennis, G
    Sherman, BT
    Hosack, DA
    Yang, J
    Gao, W
    Lane, HC
    Lempicki, RA
    [J]. GENOME BIOLOGY, 2003, 4 (09)
  • [10] Dongre AR, 2001, EUR J IMMUNOL, V31, P1485, DOI 10.1002/1521-4141(200105)31:5<1485::AID-IMMU1485>3.0.CO