Siman R G, Klein W L
Proc Natl Acad Sci U S A. 1979 Aug;76(8):4141-5. doi: 10.1073/pnas.76.8.4141.
Muscarinic acetylcholine receptor activation induces a loss of muscarinic receptors from cultured neuroblastoma and embryonic chicken cerebrum cells. As measured by specific binding of [3H]quinuclidinyl benzilate, steady-state receptor concentrations decrease 75% in response to receptor-saturating concentrations of cholinomimetic drugs. Both the degree and duration of activation determine the extent of receptor loss. A method for analyzing receptor turnover, which does not rely upon protein synthesis inhibitors, shows that activated receptors have a half-life of 1.6 hr. The regulated rate of receptor disappearance begins as soon as activators are added, and the rate is maintained as long as activators are present. The receptor blocker atropine causes an increase in receptor levels in central nervous system cultures but has no effect on receptors in cultures of adrenergic neuroblastoma cells. Because spontaneous cholinergic activity is expected only in the central nervous system cultures, the increase likely reflects blockade of endogenous regulation. Cytochalasin B blocks receptor regulation, suggesting that regulation may be mediated by a process involving microfilaments.
毒蕈碱型乙酰胆碱受体激活会导致培养的神经母细胞瘤细胞和鸡胚大脑细胞中的毒蕈碱型受体丧失。通过[3H]喹核醇基苯甲酸酯的特异性结合测定,稳态受体浓度在胆碱模拟药物达到受体饱和浓度时会降低75%。激活的程度和持续时间决定了受体丧失的程度。一种不依赖蛋白质合成抑制剂来分析受体周转的方法表明,激活的受体半衰期为1.6小时。一旦加入激活剂,受体消失的调节速率就开始,并且只要激活剂存在,速率就会维持。受体阻滞剂阿托品会导致中枢神经系统培养物中受体水平升高,但对肾上腺素能神经母细胞瘤细胞培养物中的受体没有影响。由于预计仅在中枢神经系统培养物中存在自发胆碱能活性,这种升高可能反映了对内源性调节的阻断。细胞松弛素B会阻断受体调节,这表明调节可能是由涉及微丝的过程介导的。