Macintyre E A, Tatham P E, Abdul-Gaffar R, Linch D C
Department of Haematology, University College Hospital, Medical School, London, U.K.
Immunology. 1988 Jul;64(3):427-32.
Purified pertussis toxin (PPT) is a potent mitogen for human T lymphocytes and is shown to cause rapid calcium mobilization in resting T cells, a T-cell line and CD3- lymphocytes with natural killer (NK) activity. In resting T cells the PPT activation is associated with cytoplasmic alkalinization. A similar rise in intracellular free calcium ([Ca2+]i) and cytoplasmic alkalinization is observed with activation through the antigen receptor complex. The effect of PPT is unlikely to be mediated through this pathway, however, as it can mobilize calcium in lymphocytes that do not express the CD3-Ti complex. In contrast to several other cell types, re-incubation of resting human T cells with PPT, up to a dose of 100 ng/ml for 2 hr does not block subsequent agonist-induced calcium mobilization dependent on G protein-mediated phospholipase C activation. Mitogenic doses of PPT cause a modest reduction in subsequent agonist responses, but this is likely to be due to a post-activation refractory state rather than G protein inactivation.
纯化的百日咳毒素(PPT)是一种对人T淋巴细胞有强效作用的丝裂原,已证明它能使静息T细胞、一种T细胞系以及具有自然杀伤(NK)活性的CD3-淋巴细胞迅速发生钙动员。在静息T细胞中,PPT激活与细胞质碱化有关。通过抗原受体复合物激活时,细胞内游离钙([Ca2+]i)和细胞质碱化也会出现类似升高。然而,PPT的作用不太可能通过该途径介导,因为它能在不表达CD3-Ti复合物的淋巴细胞中动员钙。与其他几种细胞类型不同,用高达100 ng/ml剂量的PPT对静息人T细胞再孵育2小时,并不会阻断随后依赖G蛋白介导的磷脂酶C激活的激动剂诱导的钙动员。促有丝分裂剂量的PPT会使随后的激动剂反应适度降低,但这可能是由于激活后的不应期状态而非G蛋白失活所致。