Goto Y, Takeshita T, Sugamura K
Department of Bacteriology, Tohoku University School of Medicine, Sendai, Japan.
FEBS Lett. 1988 Nov 7;239(2):165-8. doi: 10.1016/0014-5793(88)80909-8.
We previously established a human T cell line, TPA-Mat, which can proliferate in response to not only interleukin-2 (IL-2), but also phorbol esters such as 12-O-tetradecanoylphorbol-13-acetate (TPA) and phorbol-12,13-dibutyrate (PDBu). The present study demonstrated that the PDBu-dependent growth of TPA-Mat cells was inhibited up to 90% by adenosine 3',5'-cyclic monophosphate (cAMP] raising agents such as forskolin, cholera toxin and 1-methyl-3-isobutyl-xanthine, and cAMP analogues, whereas the IL-2-stimulated TPA-Mat growth was slightly inhibited. These findings suggest that the signal transduction pathway of PDBu-induced growth, which should involve activation of protein kinase C, is sensitive to cAMP, and that it cannot be exactly identical to the signal transduction pathway of Il-2-induced growth in TPA-Mat cells.
我们先前建立了一种人T细胞系,即TPA-Mat,它不仅可以对白细胞介素-2(IL-2)产生增殖反应,还能对佛波酯如12-O-十四酰佛波醇-13-乙酸酯(TPA)和佛波醇-12,13-二丁酸酯(PDBu)产生增殖反应。本研究表明,环磷腺苷(cAMP)升高剂如福斯可林、霍乱毒素和1-甲基-3-异丁基黄嘌呤以及cAMP类似物可将TPA-Mat细胞依赖PDBu的生长抑制高达90%,而IL-2刺激的TPA-Mat生长仅受到轻微抑制。这些发现表明,PDBu诱导生长的信号转导途径(该途径应涉及蛋白激酶C的激活)对cAMP敏感,并且它与TPA-Mat细胞中IL-2诱导生长的信号转导途径并不完全相同。