Altered T cell receptor ligands trigger a subset of early T cell signals

被引:152
作者
Rabinowitz, JD
Beeson, C
Wulfing, C
Tate, K
Allen, PM
Davis, MM
McConnell, HM
机构
[1] STANFORD UNIV,HOWARD HUGHES MED INST,STANFORD,CA 94305
[2] WASHINGTON UNIV,SCH MED,CTR IMMUNOL,ST LOUIS,MO 63110
[3] WASHINGTON UNIV,SCH MED,DEPT PATHOL,ST LOUIS,MO 63110
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1074-7613(00)80489-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
TCR ligands are complexes of peptides and MHC proteins on the surfaces of APCs. Some of these ligands cause T cell proliferation (agonists), while others block it (antagonists). We compared the acid release, calcium flux, and proliferation response of helper T cells to a variety of ligands. We found that all agonist ligands but not most antagonist ligands trigger acid release, a general indicator of early cellular activation. Only a subset of ligands triggering acid release cause sustained calcium flux, and only a subset of these ligands cause T cell proliferation. Antagonist ligands and anti-CD4 antibodies both effectively block T cell proliferation. However, significantly greater antagonist ligand or antibody concentrations are required to block acid release and initial calcium influx. These data demonstrate a hierarchy of early T cell signaling steps and show that altered TCR ligands can initiate some steps while blocking the completion of others.
引用
收藏
页码:125 / 135
页数:11
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