Burgoyne R D, Pearce B
Brain Res. 1981 Aug;254(1):55-63. doi: 10.1016/0165-3806(81)90058-4.
Exposure of primary cell cultures of rat cerebellum to the muscarinic agonist carbachol led to a 50% loss in apparent muscarinic receptor number detectable in a ligand binding assay using [3H]quinuclidinyl benzilate ([3H]QNB). The loss in [3H]QNB binding was time-dependent with a half-life of 2.9 h. Examination of membrane protein phosphorylation indicated that exposure to carabachol resulted in an increase in the level of phosphorylation of 6 polypeptides. The increased phosphorylation of 3 of these polypeptides, of molecular weights, 75,000, 67,000 and 62,000, followed a similar time-course to that of carbachol-induced loss of receptor binding. These results are consistent with the idea that the muscarinic receptor regulation involves a protein phosphorylation mechanism.
将大鼠小脑的原代细胞培养物暴露于毒蕈碱激动剂卡巴胆碱后,在使用[3H]喹核醇基苯甲酸酯([3H]QNB)的配体结合试验中,可检测到的明显毒蕈碱受体数量减少了50%。[3H]QNB结合的减少具有时间依赖性,半衰期为2.9小时。对膜蛋白磷酸化的检测表明,暴露于卡巴胆碱会导致6种多肽的磷酸化水平增加。其中3种分子量分别为75,000、67,000和62,000的多肽的磷酸化增加,其时间进程与卡巴胆碱诱导的受体结合丧失相似。这些结果与毒蕈碱受体调节涉及蛋白质磷酸化机制的观点一致。