Michal Pavel, Rudajev Vladimír, El-Fakahany Esam E, Dolezal Vladimír
Institute of Physiology CAS, Prague, Czech Republic.
Eur J Pharmacol. 2009 Mar 15;606(1-3):50-60. doi: 10.1016/j.ejphar.2009.01.028. Epub 2009 Jan 29.
We investigated the influence of membrane cholesterol content on preferential and non-preferential signaling through the M(2) muscarinic acetylcholine receptor expressed in CHO cells. Cholesterol depletion by 39% significantly decreased the affinity of M(2) receptors for [(3)H]-N-methylscopolamine ([(3)H]-NMS) binding and increased B(max) in intact cells and membranes. Membranes displayed two-affinity agonist binding sites for carbachol and cholesterol depletion doubled the fraction of high-affinity binding sites. In intact cells it also reduced the rate of agonist-induced receptor internalization and changed the profile of agonist binding from a single site to two affinity states. Cholesterol enrichment by 137% had no effects on carbachol E(max) of cAMP synthesis inhibition and on cAMP synthesis stimulation and inositolphosphates (IP) accumulation at higher agonist concentrations (non-preferred pathways). On the other hand, cholesterol depletion significantly increased E(max) of cAMP synthesis inhibition or stimulation without change in potency, and decreased E(max) of IP accumulation. Noteworthy, modifications of membrane cholesterol had no effect on membrane permeability, oxidative activity, protein content, or relative expression of G(s), G(i/o), and G(q/11) alpha subunits. These results demonstrate distinct changes of M(2) receptor signaling through both preferential and non-preferential G-proteins consequent to membrane cholesterol depletion that occur at the level of receptor/G-protein/effector protein interactions in the cell membrane. The significant decrease of IP accumulation by cholesterol depletion was also observed in cells expressing M(3) receptors and by both cholesterol depletion and enrichment in cells expressing M(1) receptors indicating relevance of reduced G(q/11) signaling for the pathogenesis of Alzheimer's disease.
我们研究了膜胆固醇含量对通过CHO细胞中表达的M(2)毒蕈碱型乙酰胆碱受体进行的优先和非优先信号传导的影响。胆固醇减少39%会显著降低M(2)受体对[(3)H]-N-甲基东莨菪碱([(3)H]-NMS)结合的亲和力,并增加完整细胞和膜中的B(max)。膜显示出对卡巴胆碱的双亲和力激动剂结合位点,胆固醇减少使高亲和力结合位点的比例增加了一倍。在完整细胞中,它还降低了激动剂诱导的受体内化速率,并将激动剂结合的模式从单个位点改变为两种亲和力状态。胆固醇增加137%对较高激动剂浓度下(非优先途径)的卡巴胆碱抑制cAMP合成的E(max)以及cAMP合成刺激和肌醇磷酸(IP)积累均无影响。另一方面,胆固醇减少显著增加了cAMP合成抑制或刺激的E(max),而效力不变,并降低了IP积累的E(max)。值得注意的是,膜胆固醇的改变对膜通透性、氧化活性、蛋白质含量或G(s)、G(i/o)和G(q/11)α亚基的相对表达没有影响。这些结果表明,膜胆固醇减少导致M(2)受体通过优先和非优先G蛋白进行的信号传导发生明显变化,这种变化发生在细胞膜中受体/G蛋白/效应蛋白相互作用的水平。在表达M(3)受体的细胞中以及在表达M(1)受体的细胞中胆固醇减少和增加时均观察到胆固醇减少导致IP积累显著降低,这表明G(q/11)信号传导减少与阿尔茨海默病的发病机制相关。