Tetraspan microdomains distinct from lipid rafts enrich select peptide-MHC class II complexes

被引:185
作者
Kropshofer, H [1 ]
Spindeldreher, S
Röhn, TA
Platania, N
Grygar, C
Daniel, N
Wölp, A
Langen, H
Horejsi, V
Vogt, AB
机构
[1] Basel Inst Immunol, CH-4005 Basel, Switzerland
[2] Roche Ctr Med Genom, CH-4070 Basel, Switzerland
[3] Blood Transfus Serv, German Red Cross, D-89081 Ulm, Germany
[4] F Hoffmann La Roche Ltd, Pharmaceut Res, CH-4070 Basel, Switzerland
[5] AS CR, Inst Mol Genet, Prague 14220, Czech Republic
关键词
D O I
10.1038/ni750
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Complexes of peptide and major histocompatibility complex (MHC) class 11 are expressed on the surface of antigen-presenting cells but their molecular organization is unknown. Here we show that subsets of MHC class 11 molecules localize to membrane microdomains together with tetraspan proteins, the peptide editor HLA-DM and the costimulator CD86. Tetraspan microdomains differ from other membrane areas such as lipid rafts, as they enrich MHC class 11 molecules carrying a selected set of peptide antigens. Antigen-presenting cells deficient in tetraspan microdomains have a reduced capacity to activate CD4(+) T cells. Thus, the organization of uniformly loaded peptide-MHC class 11 complexes in tetraspan domains may be a very early event that determines both the composition of the immunological synapse and the quality of the subsequent T helper cell response.
引用
收藏
页码:61 / 68
页数:8
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