ALTERED ANTIGEN RECEPTOR SIGNALING IN ANERGIC T-CELLS FROM SELF-TOLERANT T-CELL RECEPTOR BETA-CHAIN TRANSGENIC MICE

被引:72
作者
BLACKMAN, MA
EINKEL, TH
KAPPLER, J
CAMBIER, J
MARRACK, P
机构
[1] HOWARD HUGHES MED INST,DENVER,CO
[2] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT PEDIAT,DIV BASIC SCI,DENVER,CO
[3] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT MED,DIV BASIC IMMUNOL,DENVER,CO
[4] UNIV COLORADO,HLTH SCI CTR,DEPT MICROBIOL IMMUNOL & MED,DENVER,CO 80262
[5] UNIV COLORADO,HLTH SCI CTR,DEPT BIOCHEM BIOPHYS & GENET,DENVER,CO 80262
关键词
CLONAL ANERGY; T-CELL ACTIVATION;
D O I
10.1073/pnas.88.15.6682
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
T-cell tolerance to the minor lymphocyte-stimulating antigen Mls-1a in a T-cell receptor (TcR) V-beta-8.1 transgenic line of mice is maintained by both clonal deletion and clonal anergy. Approximately 20-50% of peripheral CD4+ (but not CD8+) T cells isolated from these mice are anergic and fail to proliferate following TcR ligation. We have examined key events in T-cell signaling in peripheral T cells isolated from these mice. In this report, we show that the anergic CD4+ T cells did not mobilize calcium or express receptors for interleukin 2 (IL-2) following TcR ligation. However, the cells retained viability and functional potential because stimulation with phorbol 12-myristate 13-acetate and ionomycin bypassed the block in receptor-mediated signaling and induced IL-2 receptor expression and proliferation of the anergic cells.
引用
收藏
页码:6682 / 6686
页数:5
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