Hailman Eric, Allen Paul M
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
J Immunol. 2005 Oct 15;175(8):4847-57. doi: 10.4049/jimmunol.175.8.4847.
CD4(+)CD8(+) double-positive (DP) thymocytes express a lower level of surface TCR than do mature T cells or single-positive (SP) thymocytes. Regulation of the TCR on DP thymocytes appears to result from intrathymic signaling, as in vitro culture of these cells results in spontaneous TCR up-regulation. In this study, we examined cell spreading and cytoskeletal polarization responses that have been shown to occur in response to TCR engagement in mature T cells. Using DP thymocytes stimulated on lipid bilayers or nontransgenic thymocytes added to anti-CD3-coated surfaces, we found that cell spreading and polarization of the microtubule organizing center and the actin cytoskeleton were inefficient in freshly isolated DP thymocytes, but were dramatically enhanced after overnight culture. SP (CD4(+)) thymocytes showed efficient responses to TCR engagement, suggesting that releasing DP thymocytes from the thymic environment mimics some aspects of positive selection. The poor translation of a TCR signal to cytoskeletal responses could limit the ability of DP thymocytes to form stable contacts with APCs and may thereby regulate thymocyte selection during T cell development.
CD4(+)CD8(+)双阳性(DP)胸腺细胞表面TCR的表达水平低于成熟T细胞或单阳性(SP)胸腺细胞。DP胸腺细胞上TCR的调节似乎源于胸腺内信号传导,因为这些细胞的体外培养会导致TCR自发上调。在本研究中,我们检测了细胞铺展和细胞骨架极化反应,这些反应已被证明会在成熟T细胞中因TCR参与而发生。使用在脂质双层上刺激的DP胸腺细胞或添加到抗CD3包被表面的非转基因胸腺细胞,我们发现新鲜分离的DP胸腺细胞中细胞铺展以及微管组织中心和肌动蛋白细胞骨架的极化效率低下,但过夜培养后显著增强。SP(CD4(+))胸腺细胞对TCR参与表现出有效的反应,这表明将DP胸腺细胞从胸腺环境中释放出来模拟了阳性选择的某些方面。TCR信号向细胞骨架反应的不良转化可能会限制DP胸腺细胞与抗原呈递细胞形成稳定接触的能力,从而可能在T细胞发育过程中调节胸腺细胞选择。