Nambi P, Whitman M, Aiyar N, Crooke S T
Department of Molecular Pharmacology, SK&F Laboratories, Philadelphia, PA 19101.
Biochem J. 1988 Sep 1;254(2):449-53. doi: 10.1042/bj2540449.
Pretreatment of A-10 cells with pertussis toxin had no effect on [arginine]vasopressin-mediated inhibition of cyclic nucleotide accumulation. Pretreatment of the cells with the same concentration of pertussis toxin produced 90-95% inhibition of [32P]ADP ribosylation in membranes, suggesting that these cells possess pertussis-toxin substrate and that the toxin enters the cells to reach its site of action. The functional integrity of the pertussis-toxin substrate in these cells is confirmed by the observation that in these cell membranes increasing concentrations of GTP inhibited basal, forskolin- and NaF-stimulated adenylate cyclase activities, and this inhibition was abolished when the cells were pretreated with pertussis toxin. In addition, thrombin-mediated inhibition of isoprenaline-stimulated cyclic AMP accumulation was also inhibited by pertussis-toxin pretreatment of the cells. These data suggest that, unlike thrombin, [arginine]vasopressin-induced inhibitory effects on cyclic nucleotide accumulation in smooth-muscle cells are not mediated by pertussis-toxin substrate.
用百日咳毒素对A - 10细胞进行预处理,对[精氨酸]血管加压素介导的环核苷酸积累抑制作用没有影响。用相同浓度的百日咳毒素对细胞进行预处理,可使膜中[32P]ADP核糖基化受到90 - 95%的抑制,这表明这些细胞具有百日咳毒素底物,且毒素进入细胞并到达其作用位点。通过观察发现,在这些细胞膜中,增加GTP浓度可抑制基础的、福斯可林和氟化钠刺激的腺苷酸环化酶活性,而当细胞用百日咳毒素预处理后,这种抑制作用被消除,这证实了这些细胞中百日咳毒素底物的功能完整性。此外,细胞经百日咳毒素预处理后,凝血酶介导的对异丙肾上腺素刺激的环磷酸腺苷积累的抑制作用也受到抑制。这些数据表明,与凝血酶不同,[精氨酸]血管加压素对平滑肌细胞中环核苷酸积累的抑制作用不是由百日咳毒素底物介导的。