Cytoplasmic tail-dependent localization of CD1b antigen-presenting molecules to MIICs

被引:199
作者
Sugita, M
Jackman, RM
vanDonselaar, E
Behar, SM
Rogers, RA
Peters, PJ
Brenner, MB
Porcelli, SA
机构
[1] HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,LYMPHOCYTE BIOL SECT,DIV RHEUMATOL & IMMUNOL,BOSTON,MA 02115
[2] UNIV UTRECHT,FAC MED,DEPT CELL BIOL,UTRECHT,NETHERLANDS
[3] UNIV UTRECHT,FAC MED,INST BIOMEMBRANES,UTRECHT,NETHERLANDS
[4] HARVARD UNIV,SCH PUBL HLTH,DEPT ENVIRONM HLTH,BOSTON,MA 02115
关键词
D O I
10.1126/science.273.5273.349
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
CD1 proteins have been implicated as antigen-presenting molecules for T cell-mediated immune responses, but their intracellular localization and trafficking remain uncharacterized. CD1b, a member of this family that presents microbial lipid antigens of exogenous origin, was found to localize to endocytic compartments that included the same specialized subset of endosomes in which major histocompatibility complex (MHC) class II molecules are proposed to bind endocytosed antigens. Unlike MHC class II molecules, which traffic to antigen-loading endosomal compartments [MHC class II compartments (MIICs)] primarily as a consequence of their association with the invariant chain, localization of CD1b to these compartments was dependent on a tyrosine-based motif in its own cytoplasmic tail.
引用
收藏
页码:349 / 352
页数:4
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