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P2Y1 and P2Y12 receptor cross-talk in calcium signalling: Evidence from nonstarved and long-term serum-deprived glioma C6 cells

机译:P2Y1和P2Y12受体在钙信号传导中的相互作用:非饥饿和长期缺乏血清的神经胶质瘤C6细胞的证据

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摘要

The current work presents results of experiments on the calcium response evoked by the stimulation by extracellular nucleotides occurring in control, nonstarved glioma C6 cells and in cells after long-term (96 h) serum starvation. Three nucleotide receptors were studied: P2Y1, P2Y2 and P2Y12. Two of them, P2Y1 and P2Y2, directly stimulate calcium response. The protein level of the P2Y2 receptor did not change during the serum starvation, while P2Y1 protein level fell dramatically. Observed changes in the calcium response generated by P2Y1 are directly correlated with the receptor protein level as well as with the amount of calcium present in the intracellular calcium stores, partially depleted during starvation process. The third receptor, P2Y12, did not directly evoke calcium response, however it is activated by the same ligand as P2Y1. The experiments with AR-C69941MX, the P2Y12-specific antagonist, indicated that in control and serum-starved cells, calcium response evoked by P2Y1 receptor is potentiated by the activity of P2Y12-dependent signaling pathways. This potentiation may be mediated by P2Y12 inhibitory effect on the plasma membrane calcium pump. The calcium influx enhanced by the cooperation of P2Y1 and P2Y12 receptor activity directly depends on the capacitative calcium entrance mechanism.
机译:当前的工作提出了在对照组,非饥饿神经胶质瘤C6细胞和长期(96小时)血清饥饿后细胞中发生的细胞外核苷酸刺激引起的钙反应的实验结果。研究了三种核苷酸受体:P2Y1,P2Y2和P2Y12。其中两个P2Y1和P2Y2直接刺激钙反应。在血清饥饿期间,P2Y2受体的蛋白质水平没有变化,而P2Y1蛋白质的水平则急剧下降。观察到的由P2Y1产生的钙反应的变化与受体蛋白水平以及细胞内钙储存中存在的钙量直接相关,在饥饿过程中部分被消耗。第三个受体P2Y12不会直接引起钙反应,但是会被与P2Y1相同的配体激活。用P2Y12特异性拮抗剂AR-C69941MX进行的实验表明,在对照和血清饥饿的细胞中,P2Y12依赖性信号通路的活性增强了P2Y1受体引起的钙反应。这种增强作用可以通过对质膜钙泵的P2Y12抑制作用来介导。通过P2Y1和P2Y12受体活性的协同作用增强的钙内流直接取决于电容性钙的进入机制。

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