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Opsin-G11-Mediated Signaling Pathway for Photic Entrainment of the Chicken Pineal Circadian Clock

机译:Opsin-G11介导的信号传导对鸡松树生物钟的信号传导通路

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摘要

Light is a major environmental signal for entrainment of the circadian clock, but little is known about the intracellular phototransduction pathway triggered by light activation of the photoreceptive molecule(s) responsible for the phase shift of the clock in vertebrates. The chicken pineal gland and retina contain the autonomous circadian oscillators together with the photic entrainment pathway, and hence they represent useful experimental models for the clock system. Here we show the expression of G11α, an α subunit of heterotrimeric G-protein, in both tissues by cDNA cloning, Northern blot, and Western blot analyses. G11α immunoreactivity was colocalized with pinopsin in the chicken pineal cells and also with rhodopsin in the outer segments of retinal photoreceptor cells, suggesting functional coupling of G11α with opsins in the clock-containing photosensitive tissues. The physical interaction was examined by coimmunoprecipitation experiments, the results of which provided evidence for light- and GTP-dependent coupling between rhodopsin and G11α. To examine whether activation of endogenous G11 leads to a phase shift of the oscillator, Gq/11-coupled m1-type muscarinic acetylcholine receptor (mAChR) was ectopically expressed in the cultured pineal cells. Subsequent treatment of the cells with carbamylcholine (CCh), an agonist of mAChR, induced phase-dependent phase shifts of the melatonin rhythm in a manner very similar to the effect of light. In contrast, CCh treatment induced no measurable effect on the rhythm of nontransfected (control) cells or cells expressing Gi/o-coupled m2-type mAChR, indicating selectivity of the G-protein activation. Together, our results demonstrate the existence of a G11-mediated opsin-signaling pathway contributing to the photic entrainment of the circadian clock.
机译:光是昼夜节律时钟的夹带的主要环境信号,但是对于脊椎动物内时钟的相移负责的光敏分子的光活化触发的细胞内光转导途径知之甚少。鸡的松果体和视网膜包含自主的昼夜节律振荡器以及光合通道,因此它们代表了时钟系统的有用实验模型。在这里,我们通过cDNA克隆,Northern印迹和Western印迹分析显示了G11α(异三聚体G蛋白的α亚基)在两种组织中的表达。 G11α免疫反应性与鸡松果体细胞中的pinopsin以及视网膜感光细胞外段的视紫红质共定位,表明G11α与视蛋白在含有时钟的感光组织中的功能偶联。通过共免疫沉淀实验检查了物理相互作用,其结果提供了视紫红质和G11α之间光和GTP依赖性偶联的证据。为了检查内源性G11的激活是否导致振荡器的相移,在培养的松果细胞中异位表达了Gq / 11偶联的m1型毒蕈碱型乙酰胆碱受体(mAChR)。随后用氨甲酰胆碱(mAChR的激动剂)氨基甲酰胆碱(CCh)处理细胞,其褪黑激素节律的相变依赖于相移,其方式与光的影响非常相似。相反,CCh处理对未转染(对照)细胞或表达Gi / o偶联的m2型mAChR的细胞的节律没有可测量的影响,表明G蛋白活化的选择性。在一起,我们的结果表明存在G11介导的视蛋白信号通路有助于昼夜节律光的夹带。

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