Hepler J R, Harden T K
Biochem J. 1986 Oct 1;239(1):141-6. doi: 10.1042/bj2390141.
The efficacy of muscarinic-receptor agonists for stimulation of inositol phosphate formation and Ca2+ mobilization in intact 1321N1 human astrocytoma cells is correlated with their capacity for formation of a GTP-sensitive high-affinity binding complex in membranes from these cells [Evans, Hepler, Masters, Brown & Harden (1985) Biochem. J. 232, 751-757]. These observations prompted the proposal that a guanine nucleotide regulatory protein serves to couple muscarinic receptors to the phospholipase C involved in phosphoinositide hydrolysis in 1321N1 cells. Inositol phosphate (InsP) formation was measured in a cell-free preparation from 1321N1 cells to provide direct support for this idea. The formation of InsP3, InsP2 and InsP1 was increased in a concentration-dependent manner (K0.5 approximately 5 microM) by guanosine 5'-[gamma-thio]triphosphate (GTP[S]) in washed membranes prepared from myo-[3H]inositol-prelabelled 1321N1 cells. Both GTP[S] and guanosine 5'-[beta gamma-imido]triphosphate (p[NH]ppG) stimulated InsP formation by 2-3-fold over control; GTP, GDP and GMP were much less efficacious. Millimolar concentrations of NaF also stimulated the formation of inositol phosphates in membrane preparations from 1321N1 cells. In the presence of 10 microM-GTP[S], the muscarinic cholinergic-receptor agonist carbachol stimulated (K0.5 approximately 10 microM) the formation of InsP above that achieved with GTP[S] alone. The effect of carbachol was completely blocked by atropine. The order of potency of nucleotides for stimulation of InsP formation in the presence of 500 microM-carbachol was GTP[S] greater than p[NH]ppG greater than GTP = GDP. Pertussis toxin, at concentrations that fully ADP-ribosylate and functionally inactivate Gi (the inhibitory guanine nucleotide regulatory protein), had no effect on InsP formation in the presence of GTP[S] or GTP[S] plus carbachol. These data are consistent with the idea that a guanine nucleotide regulatory protein that is not Gi is involved in receptor-mediated stimulation of InsP formation in 1321N1 human astrocytoma cells.
毒蕈碱受体激动剂在完整的1321N1人星形细胞瘤细胞中刺激肌醇磷酸形成和Ca2+动员的效力,与其在这些细胞膜中形成对GTP敏感的高亲和力结合复合物的能力相关[埃文斯、赫普勒、马斯特斯、布朗和哈登(1985年)《生物化学杂志》232卷,751 - 757页]。这些观察结果促使人们提出,一种鸟嘌呤核苷酸调节蛋白可将毒蕈碱受体与参与1321N1细胞中磷酸肌醇水解的磷脂酶C偶联起来。在1321N1细胞的无细胞制剂中测量肌醇磷酸(InsP)的形成,以直接支持这一观点。在由肌醇-[3H]预标记的1321N1细胞制备的洗涤过的膜中,鸟苷5'-[γ-硫代]三磷酸(GTP[S])以浓度依赖的方式(K0.5约为5 microM)增加了InsP3、InsP2和InsP1的形成。GTP[S]和鸟苷5'-[βγ-亚氨基]三磷酸(p[NH]ppG)刺激InsP形成的程度比对照高2 - 3倍;GTP、GDP和GMP的效力则低得多。毫摩尔浓度的NaF也刺激了1321N1细胞膜制剂中肌醇磷酸的形成。在存在10 microM - GTP[S]的情况下,毒蕈碱胆碱能受体激动剂卡巴胆碱刺激(K0.5约为10 microM)InsP的形成,其形成量高于单独使用GTP[S]时。卡巴胆碱的作用被阿托品完全阻断。在存在500 microM - 卡巴胆碱的情况下,核苷酸刺激InsP形成的效力顺序为GTP[S]>p[NH]ppG>GTP = GDP。百日咳毒素在能使Gi(抑制性鸟嘌呤核苷酸调节蛋白)完全ADP - 核糖基化并使其功能失活的浓度下,对存在GTP[S]或GTP[S]加卡巴胆碱时的InsP形成没有影响。这些数据与以下观点一致,即一种不是Gi的鸟嘌呤核苷酸调节蛋白参与了1321N1人星形细胞瘤细胞中受体介导的InsP形成的刺激过程。