Lissy N A, Van Dyk L F, Becker-Hapak M, Vocero-Akbani A, Mendler J H, Dowdy S F
Howard Hughes Medical Institute, Department of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Immunity. 1998 Jan;8(1):57-65. doi: 10.1016/s1074-7613(00)80458-6.
Deletion of antigen-activated T cells after an immune response and during peripheral negative selection after strong T cell receptor (TCR) engagement of cycling T cells occurs by an apoptotic process termed TCR antigen-induced cell death (AID). By analyzing the timing of death, cell cycle markers, BrdU-labeled S phase cells, and phase-specific centrifugally elutriated cultures from stimulated Jurkat T cells and peripheral blood lymphocytes, we found that AID occurs from a late G1 check point prior to activation of cyclin E:Cdk2 complexes. T cells stimulated to undergo AID can be rescued by effecting an early G1 block by direct transduction of p16INK4a tumor suppressor protein or by inactivation of the retinoblastoma tumor suppressor protein (pRb) by transduced HPV E7 protein. These results suggest that AID occurs from a late G1 death check point in a pRb-dependent fashion.
免疫反应后以及循环T细胞的T细胞受体(TCR)强烈结合后外周阴性选择期间,抗原激活的T细胞的清除是通过一种称为TCR抗原诱导细胞死亡(AID)的凋亡过程发生的。通过分析来自受刺激的Jurkat T细胞和外周血淋巴细胞的死亡时间、细胞周期标志物、BrdU标记的S期细胞以及特定阶段的离心淘洗培养物,我们发现AID发生于细胞周期蛋白E:Cdk2复合物激活之前的G1晚期检查点。通过直接转导p16INK4a肿瘤抑制蛋白实现早期G1期阻滞,或通过转导HPV E7蛋白使视网膜母细胞瘤肿瘤抑制蛋白(pRb)失活,可挽救被刺激发生AID的T细胞。这些结果表明,AID以pRb依赖的方式发生于G1晚期死亡检查点。