Treves S, Di Virgilio F, Cerundolo V, Zanovello P, Collavo D, Pozzan T
J Exp Med. 1987 Jul 1;166(1):33-42. doi: 10.1084/jem.166.1.33.
Reports from a number of laboratories have shown that mAbs against the T3-Ti receptor complex cause an increase in cytosolic-free Ca2+ [( Ca2+]i) and the hydrolysis of phosphatidylinositolbisphosphate (PIP2) in CTLs. In the present report we show that activation of CTLs by their specific targets causes: (a) release of Ca2+ from intracellular stores; (b) transient formation of inositol trisphosphate (InsP3); and (c) an increased permeability to Ca2+ of CTL plasma membrane. Killing of unrelated targets could be induced by cocentrifugation of the unrelated targets with CTLs in the presence of A23187 or PMA. We conclude that: (a) activation of CTLs by specific antigens triggers the generation of the same intracellular mediators generated by stimulation of lymphocytes with anti-T3-Ti receptor antibodies and/or with polyclonal mitogens; and (b) intracellular signals that mediate the delivery of the lethal hit by CTLs are indistinguishable from those that induce cell proliferation.
多个实验室的报告表明,针对T3-Ti受体复合物的单克隆抗体可导致细胞毒性T淋巴细胞(CTL)胞质游离钙离子浓度([Ca2+]i)升高以及磷脂酰肌醇二磷酸(PIP2)水解。在本报告中,我们表明CTL被其特异性靶标激活会导致:(a)细胞内储存的Ca2+释放;(b)肌醇三磷酸(InsP3)的短暂形成;以及(c)CTL质膜对Ca2+的通透性增加。在A23187或佛波酯(PMA)存在的情况下,通过将无关靶标与CTL共同离心可诱导对无关靶标的杀伤。我们得出以下结论:(a)特异性抗原激活CTL会触发与用抗T3-Ti受体抗体和/或多克隆有丝分裂原刺激淋巴细胞所产生的相同细胞内介质的产生;(b)介导CTL致命打击传递的细胞内信号与诱导细胞增殖的信号无法区分。