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细胞外钙和pH值对小脑微粒体组分中肌醇三磷酸介导的钙释放的影响。

The effect of external calcium and pH on inositol trisphosphate-mediated calcium release from cerebellum microsomal fractions.

作者信息

Joseph S K, Rice H L, Williamson J R

机构信息

Department of Biochemistry and Biophysics, University of Pennsylvania School of Medicine, Philadelphia 19104.

出版信息

Biochem J. 1989 Feb 15;258(1):261-5. doi: 10.1042/bj2580261.

Abstract

Binding of D-myo-inositol 1,4,5-trisphosphate (InsP3) to rat cerebellum membranes has previously been shown to be stimulated by alkaline pH and inhibited by low concentrations of Ca2+ [Worley, Baraban, Suppatopone, Wilson & Snyder (1987) J. Biol. Chem. 262, 12132-12136]. In the present study, Scatchard analysis of InsP3 binding to cerebellum microsomes indicates that the effects of Ca2+ and pH are exerted through changes in the apparent affinity of the receptor without effects on maximal binding. The influence of extravesicular Ca2+ and pH on InsP3-mediated 45Ca2+ release was investigated. Extravesicular Ca2+ inhibited InsP3-mediated Ca2+ release. The inhibitory effect of Ca2+ was most marked when a sub-optimal concentration of InsP3 was used. An increase in extravesicular pH produced a decrease in the concentration of InsP3 that yielded half-maximal Ca2+ release. Regulation of the affinity of the InsP3 receptor by Ca2+ and pH can qualitatively account for the observed effects of these factors on InsP3-mediated Ca2+ release. Feedback inhibition of InsP3 binding by Ca2+ could provide a mechanism to generate Ca2+ oscillations, particularly under hormonal conditions that produce sub-optimal elevations of InsP3 concentration.

摘要

先前已表明,D-肌醇1,4,5-三磷酸(InsP3)与大鼠小脑膜的结合受到碱性pH的刺激,并受到低浓度Ca2+的抑制[沃利、巴拉班、苏帕托波内、威尔逊和斯奈德(1987年)《生物化学杂志》262, 12132 - 12136]。在本研究中,对InsP3与小脑微粒体结合的斯卡查德分析表明,Ca2+和pH的作用是通过受体表观亲和力的变化来发挥的,而对最大结合量没有影响。研究了细胞外Ca2+和pH对InsP3介导的45Ca2+释放的影响。细胞外Ca2+抑制InsP3介导的Ca2+释放。当使用次优浓度的InsP3时,Ca2+的抑制作用最为明显。细胞外pH的升高导致产生最大Ca2+释放量一半时的InsP3浓度降低。Ca2+和pH对InsP3受体亲和力的调节可以定性地解释这些因素对InsP3介导的Ca2+释放的观察到的影响。Ca2+对InsP3结合的反馈抑制可以提供一种产生Ca2+振荡的机制,特别是在产生次优InsP3浓度升高的激素条件下。

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