Cilio C M, Daws M R, Malashicheva A, Sentman C L, Holmberg D
Department for Cell and Molecular Biology, Umeâ University, S-901 87 Umeâ, Sweden.
J Exp Med. 1998 Oct 5;188(7):1239-46. doi: 10.1084/jem.188.7.1239.
The development of a normal T cell repertoire in the thymus is dependent on the interplay between signals mediating cell survival (positive selection) and cell death (negative selection or death by neglect). Although the CD28 costimulatory molecule has been implicated in this process, it has been difficult to establish a role for the other major costimulatory molecule, cytotoxic T lymphocyte antigen (CTLA)-4. Here we report that in vivo stimulation through the T cell receptor (TCR)-CD3 complex induces expression of CTLA-4 in thymocytes and leads to the association of CTLA-4 with the SH2 domain-containing phosphatase (SHP)-2 tyrosine phosphatase. Moreover, intrathymic CTLA-4 blockade dramatically inhibits anti-CD3-mediated depletion of CD4+CD8+ double positive immature thymocytes. Similarly, anti-CD3-mediated depletion of CD4+CD8+ double positive cells in fetal thymic organ cultures could also be inhibited by anti-CTLA-4 antibodies. Thus, our data provide evidence for a role of CTLA-4 in thymic selection and suggest a novel mechanism contributing to the regulation of TCR-mediated selection of T cell repertoires.
胸腺中正常T细胞库的发育依赖于介导细胞存活(阳性选择)和细胞死亡(阴性选择或忽视性死亡)的信号之间的相互作用。尽管CD28共刺激分子已被认为参与这一过程,但要确定另一种主要共刺激分子细胞毒性T淋巴细胞抗原(CTLA)-4的作用却很困难。在此我们报告,通过T细胞受体(TCR)-CD3复合物进行的体内刺激可诱导胸腺细胞中CTLA-4的表达,并导致CTLA-4与含SH2结构域的磷酸酶(SHP)-2酪氨酸磷酸酶结合。此外,胸腺内CTLA-4阻断可显著抑制抗CD3介导的CD4+CD8+双阳性未成熟胸腺细胞的耗竭。同样,抗CTLA-4抗体也可抑制胎儿胸腺器官培养物中抗CD3介导的CD4+CD8+双阳性细胞的耗竭。因此,我们的数据为CTLA-4在胸腺选择中的作用提供了证据,并提示了一种有助于调节TCR介导的T细胞库选择的新机制。