CD81 expressed on human thymocytes mediates integrin activation and interleukin 2-dependent proliferation

被引:83
|
作者
Todd, SC
Lipps, SG
Crisa, L
Salomon, DR
Tsoukas, CD
机构
[1] SAN DIEGO STATE UNIV, DEPT BIOL, SAN DIEGO, CA 92182 USA
[2] SAN DIEGO STATE UNIV, INST MOL BIOL, SAN DIEGO, CA 92182 USA
[3] Scripps Res Inst, DEPT IMMUNOL, LA JOLLA, CA 92037 USA
[4] Scripps Res Inst, DEPT MOL & EXPT MED, LA JOLLA, CA 92037 USA
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 1996年 / 184卷 / 05期
关键词
D O I
10.1084/jem.184.5.2055
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lymphocyte recognition of antigen by the antigen-specific T cell receptor (TCR) and coreceptor complexes rapidly alters the cell's adhesive properties facilitating high avidity cell-ligand interactions necessary for lymphocyte development and function. Here, we report the expression of CD81 (target of antiproliferative antigen [TAPA]-1) on human thymocytes and the physical association of CD81 with CD4 and CD8 T cell coreceptors. Antibody ligation of CD81 on thymocytes promotes the rapid induction of integrin-mediated cell-cell adhesion via lymphocyte function-associated molecule-1 (LFA-1). Cross-linking CD81 is also shown to be costimulatory with signaling through the TCR/CD3 complex inducing interleukin 2-dependent thymocyte proliferation. These data suggest that a CD81-mediated pathway in thymocytes is involved in the regulation of both cell adhesion and activation.
引用
收藏
页码:2055 / 2060
页数:6
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