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平滑肌中功能上分离的细胞内钙库。

Functionally separate intracellular Ca2+ stores in smooth muscle.

作者信息

Flynn E R, Bradley K N, Muir T C, McCarron J G

机构信息

Neuroscience and Biomedical Systems, Institute of Biomedical and Life Sciences, West Medical Bldg., University of Glasgow, Glasgow G12 8QQ, United Kingdom.

出版信息

J Biol Chem. 2001 Sep 28;276(39):36411-8. doi: 10.1074/jbc.M104308200. Epub 2001 Jul 26.

Abstract

In smooth muscle, release via the inositol 1,4,5-trisphosphate (Ins(1,4,5)P(3)R) and ryanodine receptors (RyR) on the sarcoplasmic reticulum (SR) controls oscillatory and steady-state cytosolic Ca(2+) concentrations (Ca(2+)). The interplay between the two receptors, itself determined by their organization on the SR, establishes the time course and spatial arrangement of the Ca(2+) signal. Whether or not the receptors are co-localized or distanced from each other on the same store or whether they exist on separate stores will significantly affect the Ca(2+) signal produced by the SR. To date these matters remain unresolved. The functional arrangement of the RyR and Ins(1,4,5)P(3)R on the SR has now been examined in isolated single voltage-clamped colonic myocytes. Depletion of the ryanodine-sensitive store, by repeated application of caffeine, in the presence of ryanodine, abolished the response to Ins(1,4,5)P(3), suggesting that Ins(1,4,5)P(3)R and RyR share a common Ca(2+) store. Ca(2+) release from the Ins(1,4,5)P(3)R did not activate Ca(2+)-induced Ca(2+) release at the RyR. Depletion of the Ins(1,4,5)P(3)-sensitive store, by the removal of external Ca(2+), on the other hand, caused only a small decrease ( approximately 26%) in caffeine-evoked Ca(2+) transients, suggesting that not all RyR exist on the common store shared with Ins(1,4,5)P(3)R. Dependence of the stores on external Ca(2+) for replenishment also differed; removal of external Ca(2+) depleted the Ins(1,4,5)P(3)-sensitive store but caused only a slight reduction in caffeine-evoked transients mediated at RyR. Different mechanisms are presumably responsible for the refilling of each store. Refilling of both Ins(1,4,5)P(3)-sensitive and caffeine-sensitive Ca(2+) stores was inhibited by each of the SR Ca(2+) ATPase inhibitors thapsigargin and cyclopiazonic acid. These results may be explained by the existence of two functionally distinct Ca(2+) stores; the first expressing only RyR and refilled from Ca(2+), the second expressing both Ins(1,4,5)P(3)R and RyR and dependent upon external Ca(2+) for refilling.

摘要

在平滑肌中,通过肌醇1,4,5 - 三磷酸(Ins(1,4,5)P(3)R)和肌浆网(SR)上的兰尼碱受体(RyR)释放钙离子,可控制振荡性和稳态的胞质钙离子浓度([Ca(2+)]c)。这两种受体之间的相互作用,本身由它们在肌浆网上的组织形式决定,确立了钙离子信号的时间进程和空间分布。这些受体在同一储存库上是共定位还是彼此分开,或者它们是否存在于不同的储存库中,将显著影响肌浆网产生的钙离子信号。迄今为止,这些问题仍未得到解决。现在,已在分离的单个电压钳制结肠肌细胞中研究了肌浆网上RyR和Ins(1,4,5)P(3)R的功能排列。在存在兰尼碱的情况下,通过重复应用咖啡因耗尽对兰尼碱敏感的储存库,消除了对Ins(1,4,5)P(3)的反应,这表明Ins(1,4,5)P(3)R和RyR共享一个共同的钙离子储存库。从Ins(1,4,5)P(3)R释放的钙离子未激活RyR处的钙诱导钙释放。另一方面,通过去除细胞外钙离子耗尽对Ins(1,4,5)P(3)敏感的储存库,仅使咖啡因诱发的钙离子瞬变有小幅下降(约26%),这表明并非所有RyR都存在于与Ins(1,4,5)P(3)R共享的共同储存库中。储存库对细胞外钙离子补充的依赖性也有所不同;去除细胞外钙离子会耗尽对Ins(1,4,5)P(3)敏感的储存库,但仅使由RyR介导的咖啡因诱发的瞬变有轻微减少。推测每种储存库的重新填充由不同机制负责。对Ins(1,4,5)P(3)敏感和对咖啡因敏感的钙离子储存库的重新填充均受到肌浆网钙离子ATP酶抑制剂毒胡萝卜素和环匹阿尼酸的抑制。这些结果可以通过存在两种功能不同的钙离子储存库来解释;第一种仅表达RyR并从[Ca(2+)]c重新填充,第二种同时表达Ins(1,4,5)P(3)R和RyR并依赖细胞外钙离子进行重新填充。

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