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去表皮犬心脏浦肯野细胞肌浆网钙诱导钙释放激活和失活的时间及钙依赖性

Time and calcium dependence of activation and inactivation of calcium-induced release of calcium from the sarcoplasmic reticulum of a skinned canine cardiac Purkinje cell.

作者信息

Fabiato A

出版信息

J Gen Physiol. 1985 Feb;85(2):247-89. doi: 10.1085/jgp.85.2.247.

Abstract

Microprocessor-controlled changes of [free Ca2+] at the outer surface of the sarcoplasmic reticulum (SR) wrapped around individual myofibrils of a skinned canine cardiac Purkinje cell and aequorin bioluminescence recording were used to study the mechanism of Ca2+-induced release of Ca2+ from the SR. This Ca2+ release is triggered by a rapid increase of [free Ca2+] at the outer surface of the SR of a previously quiescent skinned cell. Ca2+-induced release of Ca2+ occurred under conditions that prevented any synthesis of ATP from ADP, was affected differentially by interventions that depressed the SR Ca2+ pump about equally, and required ionic conditions incompatible with all known Ca2+-releasing, uncoupled, partial reactions of the Ca2+ pump. Increasing the [free Ca2+]trigger up to an optimum increased the amount of Ca2+ released. A supraoptimum increase of [free Ca2+] trigger inactivated Ca2+-induced release of Ca2+, but partial inactivation was also observed at [free Ca2+] below that necessary for its activation. The amplitude of the Ca2+ release induced by a given increase of [free Ca2+] decreased when the rate of this increase was diminished. These results suggest that Ca2+-induced release of Ca2+ is through a channel across the SR membrane with time- and Ca2+-dependent activation and inactivation. The inactivating binding site would have a higher affinity for Ca2+ but a lower rate constant than the activating site. Inactivation appeared to be a first-order kinetic reaction of Ca2+ binding to a single site at the outer face of the SR with a Q10 of 1.68. The removal of inactivation was the slowest step of the cycle, responsible for a highly temperature-dependent (Q10 approximately 4.00) refractory period.

摘要

利用微处理器控制包裹在去表皮犬心脏浦肯野细胞单个肌原纤维周围的肌浆网(SR)外表面的[游离Ca2+]变化以及水母发光蛋白生物发光记录,研究Ca2+诱导的Ca2+从SR释放的机制。这种Ca2+释放是由先前静止的去表皮细胞的SR外表面的[游离Ca2+]快速增加触发的。Ca2+诱导的Ca2+释放在阻止ADP合成ATP的条件下发生,受到同等程度抑制SR Ca2+泵的干预的不同影响,并且需要与所有已知的Ca2+释放、解偶联、Ca2+泵的部分反应不兼容的离子条件。将[游离Ca2+]触发值增加到最佳值会增加Ca2+释放量。[游离Ca2+]触发值超最佳增加会使Ca2+诱导的Ca2+释放失活,但在低于其激活所需的[游离Ca2+]时也观察到部分失活。当[游离Ca2+]给定增加的速率减小时,由其增加诱导的Ca2+释放幅度减小。这些结果表明,Ca2+诱导的Ca2+释放是通过SR膜上的一个通道进行的,具有时间和Ca2+依赖性的激活和失活。失活结合位点对Ca2+的亲和力较高,但速率常数低于激活位点。失活似乎是Ca2+与SR外表面单个位点结合的一级动力学反应,Q10为1.68。失活的消除是循环中最慢的步骤,导致高度温度依赖性(Q10约为4.00)的不应期。

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