Todd S C, Lipps S G, Crisa L, Salomon D R, Tsoukas C D
Department of Biology and Molecular Biology Institute, San Diego State University, California 92182-4614, USA.
J Exp Med. 1996 Nov 1;184(5):2055-60. doi: 10.1084/jem.184.5.2055.
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.
抗原特异性T细胞受体(TCR)和共受体复合物对淋巴细胞对抗原的识别迅速改变细胞的黏附特性,促进淋巴细胞发育和功能所需的高亲和力细胞-配体相互作用。在此,我们报告了CD81(抗增殖抗原[TAPA]-1的靶点)在人胸腺细胞上的表达以及CD81与CD4和CD8 T细胞共受体的物理关联。胸腺细胞上CD81的抗体连接通过淋巴细胞功能相关分子-1(LFA-1)促进整合素介导的细胞-细胞黏附的快速诱导。交联CD81还显示出与通过TCR/CD3复合物诱导白细胞介素2依赖性胸腺细胞增殖的信号传导具有共刺激作用。这些数据表明,胸腺细胞中由CD81介导的途径参与细胞黏附和激活的调节。