Hughes A R, Martin M W, Harden T K
Proc Natl Acad Sci U S A. 1984 Sep;81(18):5680-4. doi: 10.1073/pnas.81.18.5680.
It has been proposed elsewhere [Meeker, R.B. & Harden, T. K. (1982) Mol. Pharmacol. 22, 310-319] that muscarinic cholinergic receptor-mediated attenuation of cAMP accumulation occurs through activation of phosphodiesterase in 1321N1 human astrocytoma cells. Pertussis toxin, which ADP-ribosylates the guanine nucleotide regulatory protein involved in receptor-mediated inhibition of adenylate cyclase (Ni), has been utilized to further differentiate between the mechanism of cholinergic regulation of cAMP metabolism in 1321N1 cells and the mechanism involving inhibition of adenylate cyclase in other tissues. Muscarinic receptor-mediated regulation of cAMP accumulation in NG108-15 neuroblastoma-glioma cells occurs through inhibition of adenylate cyclase. Pretreatment of these cells with pertussis toxin completely blocked the capacity of carbachol to attenuate cAMP accumulation. In contrast, concentrations of pertussis toxin two to three orders of magnitude higher than those effective in NG108-15 cells had no effect on muscarinic receptor-mediated attentuation of cAMP accumulation in 1321N1 cells. In addition, no effect of pertussis toxin was observed either on the control rate or the carbachol-stimulated rate of cAMP degradation measured directly in intact 1321N1 cells. A 41,000 Mr protein previously proposed to be the alpha subunit of Ni was labeled during incubation of a plasma membrane fraction from 1321N1 cells with [32P]NAD and pertussis toxin. Pertussis toxin is apparently active in 1321N1 cells, since this protein substrate was not labeled in plasma membrane preparations from cells previously incubated with toxin. Functional activity of Ni was demonstrated by the observation that guanosine 5'-[gamma-thio]triphosphate- and GTP-mediated inhibition of forskolin-stimulated adenylate cyclase activity occurred in cell-free preparations from 1321N1 cells. The inhibitory activity of these guanine nucleotides was lost in membrane preparations from pertussis toxin-treated cells. The data suggest that adenylate cyclase is not involved in cholinergic action in 1321N1 cells and, furthermore, Ni is not involved in muscarinic receptor-mediated activation of phosphodiesterase in these cells. Thus, pertussis toxin can be used to differentiate between two mechanisms of cholinergic regulation of cAMP metabolism.
此前在其他地方已有人提出[米克,R.B. & 哈登,T.K.(1982年)《分子药理学》22卷,310 - 319页],在1321N1人星形细胞瘤细胞中,毒蕈碱胆碱能受体介导的环磷酸腺苷(cAMP)积累的衰减是通过磷酸二酯酶的激活实现的。百日咳毒素可使参与受体介导的腺苷酸环化酶抑制作用的鸟嘌呤核苷酸调节蛋白(Ni)发生ADP核糖基化,已被用于进一步区分1321N1细胞中cAMP代谢的胆碱能调节机制与其他组织中涉及腺苷酸环化酶抑制的机制。毒蕈碱受体介导的NG108 - 15神经母细胞瘤 - 胶质瘤细胞中cAMP积累的调节是通过抑制腺苷酸环化酶实现的。用百日咳毒素预处理这些细胞可完全阻断卡巴胆碱减弱cAMP积累的能力。相比之下,比在NG108 - 15细胞中有效的浓度高两到三个数量级的百日咳毒素浓度对1321N1细胞中毒蕈碱受体介导的cAMP积累的衰减没有影响。此外,在直接测量完整的1321N1细胞中cAMP降解的对照速率或卡巴胆碱刺激的速率时,也未观察到百日咳毒素的作用。一种先前被认为是Ni的α亚基的41,000 Mr蛋白,在1321N1细胞的质膜部分与[32P]NAD和百日咳毒素一起孵育时被标记。百日咳毒素在1321N1细胞中显然具有活性,因为在先前用毒素孵育的细胞的质膜制剂中该蛋白质底物未被标记。通过观察在1321N1细胞的无细胞制剂中发生鸟苷5'-[γ - 硫代]三磷酸(GTPγS)和GTP介导的对福斯可林刺激的腺苷酸环化酶活性的抑制,证明了Ni的功能活性。在百日咳毒素处理的细胞的膜制剂中,这些鸟嘌呤核苷酸的抑制活性丧失。数据表明,腺苷酸环化酶不参与1321N1细胞中的胆碱能作用,此外,Ni不参与这些细胞中毒蕈碱受体介导的磷酸二酯酶激活。因此,百日咳毒素可用于区分cAMP代谢的胆碱能调节的两种机制。