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N-甲基-D-天冬氨酸受体对单个小脑颗粒神经元中毒蕈碱受体刺激的肌醇1,4,5-三磷酸生成及蛋白激酶C激活的调节作用

NMDA-receptor regulation of muscarinic-receptor stimulated inositol 1,4,5-trisphosphate production and protein kinase C activation in single cerebellar granule neurons.

作者信息

Young Kenneth W, Garro M Asier, Challiss R A John, Nahorski Stefan R

机构信息

Department of Cell Physiology and Pharmacology, University of Leicester, Medical Sciences Building, University Road, Leicester LE1 9HN, UK.

出版信息

J Neurochem. 2004 Jun;89(6):1537-46. doi: 10.1111/j.1471-4159.2004.02458.x.

Abstract

Inositol 1,4,5-trisphosphate (InsP(3)) production in single cerebellar granule neurons (CGNs) grown in culture was measured using the PH domain of phospholipase C delta1 tagged with enhanced green fluorescent protein (eGFP-PH(PLCdelta1)). These measurements were correlated with changes in intracellular free Ca2+ determined by single cell imaging. In control CGNs, intracellular Ca2+ stores appeared replete. However, the refilling state of these stores appeared dependent on the fluorophore used to measure Ca2+-release. Thus, methacholine (MCH), acting via muscarinic acetylcholine-receptors (mAchRs), mobilised intracellular Ca2+ in cells loaded with fluo-3 and fura-4f, but not fura-2. Confocal measurements of single CGNs expressing eGFP-PH(PLCdelta1) demonstrated that MCH stimulated a robust peak increase in InsP(3), which was followed by a sustained plateau phase of InsP(3) production. In contrast, glutamate-induced InsP(3) signals were weak or not detectable. MCH-stimulated InsP(3) production was reduced by chelation of intracellular Ca2+ with BAPTA, and emptying of intracellular stores with thapsigargin, indicated a positive feedback effect of Ca2+ mobilisation onto PLC activity. In CGNs, NMDA- and KCl-mediated Ca2+-entry significantly enhanced MCH-induced InsP(3) production. Furthermore, mAchR-mediated PLC activation appeared sensitive to the full dynamic range of intracellular Ca2+ increases stimulated by 100 microm NMDA. This dynamic regulation was also observed at the level of PKC activation indicated by an enhanced translocation of eGFP-tagged myristoylated alanine-rich C kinase substrate (MARCKS) protein in cells stimulated with MCH. Thus, NMDA-mediated Ca2+ influx and PLC activation may represent a coincident-detection system whereby ionotropic and metabotropic signals combine to stimulate InsP(3) production and PKC-mediated phosphorylation events in CGNs.

摘要

利用增强型绿色荧光蛋白标记的磷脂酶Cδ1的PH结构域(eGFP-PH(PLCδ1)),测量培养的单个小脑颗粒神经元(CGNs)中肌醇1,4,5-三磷酸(InsP(3))的产生。这些测量结果与通过单细胞成像确定的细胞内游离Ca2+的变化相关。在对照CGNs中,细胞内Ca2+储存似乎充足。然而,这些储存的再填充状态似乎取决于用于测量Ca2+释放的荧光团。因此,通过毒蕈碱型乙酰胆碱受体(mAchRs)起作用的乙酰甲胆碱(MCH),在装载了fluo-3和fura-4f但未装载fura-2的细胞中动员细胞内Ca2+。对表达eGFP-PH(PLCδ1)的单个CGNs进行共聚焦测量表明,MCH刺激InsP(3)出现强烈的峰值增加,随后是InsP(3)产生的持续平台期。相比之下,谷氨酸诱导的InsP(3)信号较弱或无法检测到。用BAPTA螯合细胞内Ca2+以及用毒胡萝卜素排空细胞内储存,可降低MCH刺激的InsP(3)产生,这表明Ca2+动员对PLC活性有正反馈作用。在CGNs中,NMDA和KCl介导的Ca2+内流显著增强了MCH诱导的InsP(3)产生。此外,mAchR介导的PLC激活似乎对100微摩尔NMDA刺激的细胞内Ca2+增加的整个动态范围敏感。在用MCH刺激的细胞中,eGFP标记的豆蔻酰化富含丙氨酸的C激酶底物(MARCKS)蛋白的转位增强,这表明在PKC激活水平也观察到了这种动态调节。因此,NMDA介导的Ca2+内流和PLC激活可能代表一种同时检测系统,通过该系统离子型和代谢型信号结合起来刺激CGNs中InsP(3)的产生和PKC介导的磷酸化事件。

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