Suda T, Tanaka M, Miwa K, Nagata S
Osaka Bioscience Institute, Department of Molecular Biology, Japan.
J Immunol. 1996 Nov 1;157(9):3918-24.
We have investigated the susceptibility of mouse T cells at various maturation and activation stages to recombinant soluble mouse Fas ligand (termed WX1). CD4+CD8+ thymocytes were preferentially killed by WX1, although CD4+CD8- and CD4-CD8+ thymocytes were also killed at higher concentrations of WX1. The majority of CD4-CD8- thymocytes were resistant to the same doses of WX1. Naive peripheral T cells were also killed by WX1 at concentrations similar to those for single-positive thymocytes. Activation-induced cell death of previously activated T cells is known to be mediated by Fas and Fas ligand. However, the activation of naive splenic T cells by mAbs against CD3/TCR complex rather induced resistance against WX1. This resistance was induced in activated T cells but not in bystander T cells. These mechanisms seem to explain why activated T cells are not immediately killed and why bystander T cells are not activated in an Ag-nonspecific manner.
我们研究了处于不同成熟和激活阶段的小鼠T细胞对重组可溶性小鼠Fas配体(称为WX1)的敏感性。CD4+CD8+胸腺细胞优先被WX1杀伤,不过在更高浓度的WX1作用下,CD4+CD8-和CD4-CD8+胸腺细胞也会被杀伤。大多数CD4-CD8-胸腺细胞对相同剂量的WX1具有抗性。初始外周T细胞也会被WX1杀伤,其浓度与单阳性胸腺细胞的相似。已知先前激活的T细胞的激活诱导细胞死亡是由Fas和Fas配体介导的。然而,用抗CD3/TCR复合物的单克隆抗体激活初始脾T细胞反而诱导了对WX1的抗性。这种抗性在激活的T细胞中诱导产生,而在旁观者T细胞中则不会。这些机制似乎可以解释为什么激活的T细胞不会立即被杀伤,以及为什么旁观者T细胞不会以抗原非特异性的方式被激活。