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基于沿渗透途径的调节性钙结合位点的模型中的量子释放、增量检测和长周期钙离子振荡。

Quantal release, incremental detection, and long-period Ca2+ oscillations in a model based on regulatory Ca2+-binding sites along the permeation pathway.

作者信息

Dupont G, Swillens S

机构信息

Unité de Chronobiologie Théorique, Faculté des Sciences, Université Libre de Bruxelles, Brussels, Belgium.

出版信息

Biophys J. 1996 Oct;71(4):1714-22. doi: 10.1016/S0006-3495(96)79373-6.

Abstract

Quantal release, incremental detection, and oscillations are three types of Ca2+ responses that can be obtained in different conditions, after stimulation of the intracellular Ca2+ stores by submaximum concentrations of inositol 1,4,5-triphosphate (InsP3). All three phenomena are thought to occur through the regulatory properties of the InsP3 receptor/Ca2+ channel. In the present study, we perform further analysis of the model (Swillens et al., 1994, Proc. Natl. Acad. Sci. USA. 91:10074-10078) previously proposed for transient InsP3-induced Ca2+ release, based on the bell-shaped dependence of the InsP3 receptor activity on the Ca2+ level and on the existence of an intermediate Ca2+ domain located around the mouth of the channel. We show that Ca2+ oscillations also arise in the latter model. Conditions for the occurrence of the various behaviors are investigated. Numerical simulations also show that the existence of an intermediate Ca2+ domain can markedly increase the period of oscillations. Periods on the order of 1 min can indeed be accounted for by the model when one assigns realistic values to the kinetic constants of the InsP3 receptor, which, in the absence of a domain, lead to oscillations with periods of a few seconds. Finally, theoretical support in favor of a positive cooperativity in the regulation of the InsP3 receptor by Ca2+ is presented.

摘要

量子释放、增量检测和振荡是三种类型的Ca2+反应,在通过次最大浓度的肌醇1,4,5-三磷酸(InsP3)刺激细胞内Ca2+储存后,在不同条件下可以获得这些反应。所有这三种现象都被认为是通过InsP3受体/Ca2+通道的调节特性发生的。在本研究中,我们对先前提出的用于瞬时InsP3诱导的Ca2+释放的模型(Swillens等人,1994年,《美国国家科学院院刊》。91:10074-10078)进行了进一步分析,该模型基于InsP3受体活性对Ca2+水平的钟形依赖性以及通道口周围存在中间Ca2+结构域。我们表明,在后者的模型中也会出现Ca2+振荡。研究了各种行为发生的条件。数值模拟还表明,中间Ca2+结构域的存在可以显著增加振荡周期。当为InsP3受体的动力学常数赋予实际值时,该模型确实可以解释大约1分钟的周期,而在没有结构域的情况下,这会导致周期为几秒的振荡。最后,提出了支持Ca2+对InsP3受体调节存在正协同作用的理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/174e/1233641/a9d929603445/biophysj00044-0064-a.jpg

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