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从肌醇三磷酸敏感钙库中自发释放钙。

Spontaneous calcium release from inositol trisphosphate-sensitive calcium stores.

作者信息

Missiaen L, Taylor C W, Berridge M J

机构信息

Department of Zoology, University of Cambridge, UK.

出版信息

Nature. 1991 Jul 18;352(6332):241-4. doi: 10.1038/352241a0.

Abstract

Inositol 1,4,5-trisphosphate (InsP3) functions as a second messenger to mobilize Ca2+ from intracellular reservoirs. The release mechanism displays all-or-none characteristics, that may account for other observations that the InsP3-induced mobilization of Ca2+ is quantal. Quantal release may depend on the sensitivity of the InsP3 receptor being regulated by the Ca2+ concentration in the lumen of the endoplasmic reticulum. We report here that the InsP3-sensitive store in hepatocytes discharges spontaneously when overloaded with Ca2+. The release, which is blocked by heparin, is preceded by an increasing sensitivity of the InsP3 receptor to endogenous InsP3, and is promoted by those sulphydryl reagents (oxidized glutathione and thimerosal) that induce Ca2+ oscillations in intact cells (ref. 8, and T. A. Rooney, D. C. Renard, E. J. Sass and A. P. Thomas, manuscript in preparation). This novel process could have a role in generating both Ca2+ oscillations and Ca2+ waves.

摘要

肌醇1,4,5-三磷酸(InsP3)作为第二信使,从细胞内储存库中动员Ca2+。释放机制表现出全或无的特征,这可能解释了其他一些观察结果,即InsP3诱导的Ca2+动员是量子化的。量子释放可能取决于内质网腔中Ca2+浓度对InsP3受体敏感性的调节。我们在此报告,当肝细胞中InsP3敏感储存库Ca2+过载时会自发释放。这种释放被肝素阻断,在释放之前InsP3受体对内源性InsP3的敏感性增加,并且被那些在完整细胞中诱导Ca2+振荡的巯基试剂(氧化型谷胱甘肽和硫柳汞)所促进(参考文献8以及T.A.鲁尼、D.C.勒纳尔、E.J.萨斯和A.P.托马斯,正在准备的手稿)。这个新过程可能在产生Ca2+振荡和Ca2+波中起作用。

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