Selectivity of the major histocompatibility complex class II presentation pathway of cortical thymic epithelial cell lines

被引:29
作者
Oukka, M
Andre, P
Turmel, P
Besnard, N
Angevin, V
Karlsson, L
Trans, PL
Charron, D
Bihain, B
Kosmatopoulos, K
Lotteau, V
机构
[1] INSERM,U391,F-35043 RENNES,FRANCE
[2] INSERM,U267,VILLEJUIF,FRANCE
[3] RW JOHNSON PHARMACEUT RES INST,SAN DIEGO,CA 92121
[4] INSERM,U25,PARIS,FRANCE
[5] INSERM,U396,PARIS,FRANCE
关键词
antigen presentation; thymus; selection;
D O I
10.1002/eji.1830270408
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Major histocompatibility complex (MHC) restriction of the immune response is established during positive selection of T cells in the thymus. This occurs mainly through interactions of T cell receptor of developing thymocytes with MHC/peptide ligands on cortical thymic epithelial cells (TEC). An ongoing controversy concerns the origin and the role of peptides involved in the positive selection of thymocytes. Evidence provided here shows that processing of MHC class II complexes in cortical TEC differs from that of medullary TEC. Removal of the invariant chain associated with MHC class II complexes was rapid and complete in medullary TEC which present peptides from both exogenous and cytosolic origin. In cortial TEC, a large fraction of class II dimers remained associated with a 10-12-kDa fragment of invariant chain (Ii). Incomplete removal of Ii correlated with the inability of cortical TEC to present peptides from exogenous origin. However, presentation of peptides from cytosolic proteins by cortical TEC remained possible. Thus, most peptides from exogenous proteins may be excluded from participating in positive selection of CD4(+) T cells by a mechanism limiting Ii breakdown.
引用
收藏
页码:855 / 859
页数:5
相关论文
共 37 条
[21]   THYMIC CORTICAL EPITHELIAL-CELLS CAN PRESENT SELF-ANTIGENS INVIVO [J].
LORENZ, RG ;
ALLEN, PM .
NATURE, 1989, 337 (6207) :560-562
[22]   T-CELL RECEPTOR V-BETA USE PREDICTS REACTIVITY AND TOLERANCE TO MLSA-ENCODED ANTIGENS [J].
MACDONALD, HR ;
SCHNEIDER, R ;
LEES, RK ;
HOWE, RC ;
ACHAORBEA, H ;
FESTENSTEIN, H ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
NATURE, 1988, 332 (6159) :40-45
[23]   PROCESSING PATHWAYS FOR PRESENTATION OF CYTOSOLIC ANTIGEN TO MHC CLASS-II-RESTRICTED T-CELLS [J].
MALNATI, MS ;
MARTI, M ;
LAVAUTE, T ;
JARAQUEMADA, D ;
BIDDISON, W ;
DEMARS, R ;
LONG, EO .
NATURE, 1992, 357 (6380) :702-704
[24]  
MALNATI MS, 1993, J IMMUNOL, V151, P6751
[25]   ENDOSOMAL ASPARTIC PROTEINASES ARE REQUIRED FOR INVARIANT-CHAIN PROCESSING [J].
MARIC, MA ;
TAYLOR, MD ;
BLUM, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2171-2175
[26]  
MARTIN DW, 1996, CELL, V84, P543
[27]   Mice lacking H2-M complexes, enigmatic elements of the MHC class II peptide-loading pathway [J].
Miyazaki, T ;
Wolf, P ;
Tourne, S ;
Waltzinger, C ;
Dierich, A ;
Barois, N ;
Ploegh, H ;
Benoist, C ;
Mathis, D .
CELL, 1996, 84 (04) :531-541
[28]   MEDULLARY BUT NOT CORTICAL THYMIC EPITHELIAL-CELLS PRESENT SOLUBLE-ANTIGENS TO HELPER T-CELLS [J].
MIZUOCHI, T ;
KASAI, M ;
KOKUHO, T ;
KAKIUCHI, T ;
HIROKAWA, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (06) :1601-1605
[30]  
NEEFJES JJ, 1992, EMBO J, V11, P414