Ucker D S, Ashwell J D, Nickas G
Division of Immunology, Medical Biology Institute, La Jolla, CA 92037.
J Immunol. 1989 Dec 1;143(11):3461-9.
We have observed that stimuli that are mitogenic for normal T cells can induce cell death in transformed T cell hybridomas. "Activation-driven cell death" can be triggered by the presentation of appropriate Ag as well as by treatment with lectins and antibodies specific for the T cell Ag receptor complex and other activation structures on the T cell surface, such as Thy-1 and Ly-6. The activation-driven lethal process is cell autonomous, is associated with a fragmentation of the cell's genome characteristic of the "suicide process" induced in immature T cells by glucocorticoids and in target cells by cytotoxic T lymphocytes, and is dependent upon transcription and translation, presumably associated with the expression of new gene products. We hypothesize that activation-driven cell death may be involved in vivo in the clonal deletion of auto-reactive T cells during T cell ontogeny.
我们已经观察到,对正常T细胞有促有丝分裂作用的刺激物可诱导转化的T细胞杂交瘤发生细胞死亡。“激活驱动的细胞死亡”可由适当抗原的呈递触发,也可通过用对T细胞抗原受体复合物以及T细胞表面其他激活结构(如Thy-1和Ly-6)具有特异性的凝集素和抗体处理来触发。激活驱动的致死过程是细胞自主的,与细胞基因组的片段化有关,这种片段化是糖皮质激素在未成熟T细胞中以及细胞毒性T淋巴细胞在靶细胞中诱导的“自杀过程”的特征,并且依赖于转录和翻译,推测与新基因产物的表达有关。我们假设激活驱动的细胞死亡可能在体内参与T细胞个体发育过程中自身反应性T细胞的克隆清除。