Zeng L, Houslay M D
Division of Biochemistry and Molecular Biology, University of Glasgow, Scotland, UK.
Biochem J. 1995 Dec 15;312 ( Pt 3)(Pt 3):769-74. doi: 10.1042/bj3120769.
Incubation of hepatocytes or the SV40-DNA-immortalized hepatocyte P9 cell line with cholera toxin led to a time-dependent activation of adenylate cyclase activity, which occurred after a defined lag period. When added together with cholera toxin, each of the hormones insulin and vasopressin was capable of attenuating the maximum stimulatory effect achieved by cholera toxin over a period of 60 min through a process which could be blocked by the compounds staurosporine and chelerythrine. Attenuating effects on cholera-toxin-stimulated adenylate cyclase activity could also be elicited by using either the protein kinase C (PKC)-stimulating phorbol ester PMA (phorbol 12-myristate 13-acetate) or the protein phosphatase inhibitor okadaic acid. Alkaline phosphatase treatment of membranes reversed the inhibitory effect of PMA. Cholera toxin also stimulated the adenylate cyclase activity of intact CHO (Chinese-hamster ovary) and NIH-3T3 cells, but this activity was insensitive to the addition of PMA. Overexpression of various PKC isoforms in CHO cell lines did not confer sensitivity to inhibition by PMA upon cholera-toxin-stimulated adenylate cyclase activity. Rather, overexpression of the gamma isoform of PKC allowed PMA to stimulate adenylate cyclase activity in CHO cells. It is suggested that the PKC-mediated phosphorylation of a membrane protein attenuates cholera-toxin-stimulated adenylate cyclase activity in hepatocytes and P9 cells. The cellular selectivity of such an action may be due to the target for this inhibitory action of PKC being a particular isoform of adenylate cyclase which provides the major activity in hepatocytes and P9 cells, but not in either CHO or NIH-3T3 cells.
用霍乱毒素孵育肝细胞或SV40 - DNA永生化的肝细胞P9细胞系,会导致腺苷酸环化酶活性呈时间依赖性激活,这一过程在特定的延迟期后发生。当与霍乱毒素一起添加时,胰岛素和血管加压素这两种激素中的每一种都能够在60分钟的时间内通过一种可被化合物星形孢菌素和白屈菜红碱阻断的过程减弱霍乱毒素所达到的最大刺激作用。使用蛋白激酶C(PKC)刺激剂佛波酯PMA(佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯)或蛋白磷酸酶抑制剂冈田酸也能引发对霍乱毒素刺激的腺苷酸环化酶活性的减弱作用。对膜进行碱性磷酸酶处理可逆转PMA的抑制作用。霍乱毒素也刺激完整的中国仓鼠卵巢(CHO)细胞和NIH - 3T3细胞的腺苷酸环化酶活性,但这种活性对添加PMA不敏感。在CHO细胞系中过表达各种PKC同工型并没有使霍乱毒素刺激的腺苷酸环化酶活性对PMA抑制产生敏感性。相反,PKC的γ同工型的过表达使PMA能够刺激CHO细胞中的腺苷酸环化酶活性。有人提出,PKC介导的膜蛋白磷酸化会减弱肝细胞和P9细胞中霍乱毒素刺激的腺苷酸环化酶活性。这种作用的细胞选择性可能是由于PKC这种抑制作用的靶点是腺苷酸环化酶的一种特定同工型,它在肝细胞和P9细胞中提供主要活性,但在CHO细胞或NIH - 3T3细胞中则不然。