Intracellular trafficking of CTLA-4 and focal localization towards sites of TCR engagement

被引:507
作者
Linsley, PS
Bradshaw, J
Greene, J
Peach, R
Bennett, KL
Mittler, RS
机构
[1] Bristol-Myers Squibb P., Seattle, WA 98121
关键词
D O I
10.1016/S1074-7613(00)80480-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T lymphocyte receptor CTLA-4 binds costimulatory molecules CD80 (B7-1) and CD86 (B7-2) with high avidity and negatively regulates T cell activation. CTLA-4 functions at the cell surface, yet is primarily localized in intracellular vesicles. Here, we demonstrate cycling of CTLA-4 between intracellular stores and the cell surface. Intracellular vesicles containing CTLA-4 over-lapped with endocytic compartment(s) and with perforin-containing secretory granules. Cell surface expression of CTLA-4 was rapidly increased by raising intracellular calcium levels. During T cell activation, intracellular and cell surface CTLA-4 became focused towards sites of TCR activation. Cycling and directional control of CTLA-4 expression may regulate its functional interaction with APCs bearing peptide-MHC complexes of appropriate specificity and avidity.
引用
收藏
页码:535 / 543
页数:9
相关论文
共 28 条