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豚鼠通透平滑肌细胞中肌醇1,4,5 -三磷酸诱导的钙离子释放的pH依赖性

pH dependence of inositol 1,4,5-trisphosphate-induced Ca2+ release in permeabilized smooth muscle cells of the guinea-pig.

作者信息

Tsukioka M, Iino M, Endo M

机构信息

Department of Pharmacology, Faculty of Medicine, University of Tokyo, Japan.

出版信息

J Physiol. 1994 Mar 15;475(3):369-75. doi: 10.1113/jphysiol.1994.sp020078.

Abstract
  1. The dependence on pH of inositol 1,4,5-trisphosphate (IP3)-induced Ca2+ release was studied in saponin-skinned smooth muscle cells from guinea-pig portal vein, using the indicator fura-2 to monitor Ca2+ release. 2. Increasing pH between 6.7 and 7.3 enhanced the rate of IP3-induced Ca2+ release at all the Ca2+ concentrations above 30 nM without changing the bell-shaped dependence of the Ca2+ release rate on Ca2+ concentration with a peak near 300 nM. 3. The ascending limb of the biphasic Ca2+ dependence was shifted slightly toward the lower Ca2+ concentration at pH 7.3, suggesting an increase in the Ca2+ sensitivity of IP3-induced Ca2+ release at the higher pH. 4. With the elevation in pH from 6.7 to 7.3 at 100 nM Ca2+, about 7-fold higher IP3 concentration was required to release half of the Ca2+ in the store within 15 s. This pH-dependent change in the IP3 sensitivity was smaller at 1 microM Ca2+ and was indiscernible in the absence of Ca2+. 5. These results suggest that H+ may inhibit binding of IP3 and Ca2+ to the modulator sites of the Ca2+ release mechanism. However, these effects on the binding sites may not fully explain the complex effect of pH, and there may be pH-dependent step(s) involved in the gating mechanism of IP3 channels. The present study demonstrates the importance of pH as a modulator of IP3-induced Ca2+ release.
摘要
  1. 使用荧光指示剂fura-2监测豚鼠门静脉皂素透化平滑肌细胞中肌醇1,4,5-三磷酸(IP3)诱导的Ca2+释放对pH的依赖性。2. 在6.7至7.3之间提高pH值,可增强所有高于30 nM的Ca2+浓度下IP3诱导的Ca2+释放速率,且不会改变Ca2+释放速率对Ca2+浓度的钟形依赖性,峰值接近300 nM。3. 在pH 7.3时,双相Ca2+依赖性的上升支略微向较低的Ca2+浓度偏移,表明在较高pH值下IP3诱导的Ca2+释放的Ca2+敏感性增加。4. 在100 nM Ca2+条件下,当pH从6.7升高到7.3时,在15秒内释放储存中一半Ca2+所需的IP3浓度大约高出7倍。在1 microM Ca2+时,这种IP3敏感性的pH依赖性变化较小,而在无Ca2+时则无法分辨。5. 这些结果表明,H+可能抑制IP3和Ca2+与Ca2+释放机制调节位点的结合。然而,这些对结合位点的影响可能无法完全解释pH的复杂作用,并且在IP3通道的门控机制中可能存在pH依赖性步骤。本研究证明了pH作为IP3诱导的Ca2+释放调节剂的重要性。

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