van de Westerlo E, Yang J, Logsdon C, Williams J A
Department of Physiology, University of Michigan, Ann Arbor 48109, USA.
Biochem J. 1995 Sep 1;310 ( Pt 2)(Pt 2):559-63.
Chinese hamster ovary cells stably transfected with human M3 muscarinic acetylcholine receptors show a 40-50% reduction in the immunoreactive G-proteins Gq alpha and G11 alpha when stimulated with the cholinergic agonist carbachol. This effect is seen after 9 h, is maximal after 24 h, and occurs over a range of carbachol concentrations that activate phosphoinositide hydrolysis in these cells. The effect is specific for Gq alpha family proteins as Gs alpha was slightly increased after carbachol treatment and G13 alpha was unchanged. Using a urea gel system, we were able to resolve Gq alpha and G11 alpha, both of which were down-regulated by carbachol. An M3 receptor mutant, with C-terminal threonines changed to alanines as described previously, binds ligand and activates phosphoinositide hydrolysis normally but is not down-regulated in response to carbachol. This receptor, however, induces Gq alpha/G11 alpha down-regulation similarly to wild-type M3 receptors, indicating that G-protein down-regulation is not directly coupled to receptor down-regulation. Thus down-regulation of Gq alpha and G11 alpha may contribute to heterologous desensitization particularly at longer times of agonist exposure.
稳定转染人M3毒蕈碱型乙酰胆碱受体的中国仓鼠卵巢细胞在用胆碱能激动剂卡巴胆碱刺激时,免疫反应性G蛋白Gqα和G11α减少40 - 50%。此效应在9小时后出现,24小时后达到最大,且在一系列能激活这些细胞中磷酸肌醇水解的卡巴胆碱浓度范围内均会发生。该效应对Gqα家族蛋白具有特异性,因为卡巴胆碱处理后Gsα略有增加,而G13α不变。使用尿素凝胶系统,我们能够分辨出Gqα和G11α,二者均被卡巴胆碱下调。如前所述,一种C末端苏氨酸突变为丙氨酸的M3受体突变体,能正常结合配体并激活磷酸肌醇水解,但对卡巴胆碱不发生下调。然而,该受体与野生型M3受体一样能诱导Gqα/G11α下调,这表明G蛋白下调并非直接与受体下调相关联。因此,Gqα和G11α的下调可能尤其在激动剂暴露较长时间时促成异源脱敏。