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雷诺丁可使心肌钙释放通道(雷诺丁受体亚型2)对钙激活敏感,并在通道因钙耗竭而关闭时解离。

Ryanodine sensitizes the cardiac Ca(2+) release channel (ryanodine receptor isoform 2) to Ca(2+) activation and dissociates as the channel is closed by Ca(2+) depletion.

作者信息

Du G G, Guo X, Khanna V K, MacLennan D H

机构信息

Banting and Best Department of Medical Research, University of Toronto, Toronto, ON, Canada M5G 1L6.

出版信息

Proc Natl Acad Sci U S A. 2001 Nov 20;98(24):13625-30. doi: 10.1073/pnas.241516898. Epub 2001 Nov 6.

Abstract

In single-channel recordings, the rabbit cardiac Ca(2+) release channel (RyR2) is converted to a fully open subconductance state with about 50% of full conductance by micromolar concentrations of ryanodine. At +30 mV, corresponding to a luminal to cytoplasmic cation current, the probability of opening (P(o)) of ryanodine-modified channels was only marginally altered at pCa 10 (pCa = -log(10) Ca concentration). However, at -30 mV, the P(o) was highly sensitive to Ca(2+) added to the cis (cytoplasmic) side and, at pCa 10, was reduced to less than 0.27. The EC(50) value for channel opening was about pCa 8. No significant Ca(2+) inactivation was observed for ryanodine-modified channels at either -30 mV or +30 mV. The opening of unmodified Ca(2+) channels is Ca(2+) sensitive, with an EC(50) value of about pCa 6 (two orders of magnitude less sensitive than ryanodine-modified channels) and IC(50) values of pCa 2.2 at -30 mV and 2.5 at +30 mV. Mg(2+) decreased the P(o) of ryanodine-modified channels at low Ca(2+) concentrations at both -30 and +30 mV. Caffeine, ATP, and ruthenium red were modulators of the P(o) of ryanodine-modified channels. In a [(3)H]ryanodine binding assay, [(3)H]ryanodine dissociation from the high-affinity binding site was found to be Ca(2+) sensitive, with an IC(50) of pCa 7.1. High concentrations of unlabeled ryanodine prevented [(3)H]ryanodine dissociation, but ruthenium red accelerated dissociation. These results suggest that ryanodine sensitizes Ca(2+) activation of the Ca(2+) release channel and desensitizes Ca(2+) inactivation through an allosteric interaction. [(3)H]Ryanodine dissociates from the high-affinity site when the channel is closed by removal of Ca(2+), implying that high-affinity ryanodine and Ca(2+) binding sites are linked through either short- or long-range interactions, probably involving conformational changes.

摘要

在单通道记录中,微摩尔浓度的ryanodine可使兔心脏钙释放通道(RyR2)转变为一种完全开放的亚电导状态,其电导约为全电导的50%。在+30 mV时,对应于从腔内向胞质的阳离子电流,在pCa 10(pCa = -log₁₀钙浓度)时,ryanodine修饰通道的开放概率(P(o))仅略有改变。然而,在 -30 mV时,P(o)对添加到顺式(胞质)侧的Ca²⁺高度敏感,在pCa 10时,降至小于0.27。通道开放的EC₅₀值约为pCa 8。在 -30 mV或 +30 mV时,未观察到ryanodine修饰通道有明显的Ca²⁺失活现象。未修饰的Ca²⁺通道的开放对Ca²⁺敏感,EC₅₀值约为pCa 6(比ryanodine修饰通道的敏感性低两个数量级),在 -30 mV时的IC₅₀值为pCa 2.2,在 +30 mV时为2.5。在 -30 mV和 +30 mV时,低Ca²⁺浓度下,Mg²⁺降低了ryanodine修饰通道的P(o)。咖啡因、ATP和钌红是ryanodine修饰通道P(o)的调节剂。在[³H]ryanodine结合试验中,发现[³H]ryanodine从高亲和力结合位点的解离对Ca²⁺敏感,IC₅₀为pCa 7.1。高浓度的未标记ryanodine可阻止[³H]ryanodine的解离,但钌红可加速解离。这些结果表明,ryanodine通过变构相互作用使钙释放通道的Ca²⁺激活敏感化,并使Ca²⁺失活脱敏。当通过去除Ca²⁺使通道关闭时,[³H]ryanodine从高亲和力位点解离,这意味着高亲和力ryanodine和Ca²⁺结合位点通过短程或长程相互作用相联系,可能涉及构象变化。

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