Suppr超能文献

内质网腔Ca2+对绵羊心脏肌浆网Ca(2+)释放通道门控的调节

Regulation of the gating of the sheep cardiac sarcoplasmic reticulum Ca(2+)-release channel by luminal Ca2+.

作者信息

Sitsapesan R, Williams A J

机构信息

Department of Cardiac Medicine, National Heart and Lung Institute, London, United Kingdom.

出版信息

J Membr Biol. 1994 Feb;137(3):215-26. doi: 10.1007/BF00232590.

Abstract

We investigated the effects of changes in luminal [Ca2+] on the gating of native and purified sheep cardiac sarcoplasmic reticulum (SR) Ca(2+)-release channels reconstituted into planar phospholipid bilayers. The open probability (Po) of channels activated solely by cytosolic Ca2+ was greater at positive than negative holding potentials. Channels activated solely by 10 microM cytosolic Ca2+ exhibited no change in steady-state Po or in the relationship between Po and voltage when the luminal [Ca2+] was increased from nanomolar to millimolar concentrations. In the absence of activating concentrations of cytosolic Ca2+, the channel can be activated by the phosphodiesterase inhibitor sulmazole (AR-L 115BS). However, cytosolic Ca(2+)-independent activation of the channel by sulmazole requires luminal Ca2+. In the presence of sulmazole, at picomolar luminal [Ca2+] the channel remains completely closed. Increasing the luminal [Ca2+] to millimolar levels markedly increases the Po via an increase in the duration of open events. The Po and duration of the sulmazole-activated, luminal Ca(2+)-dependent channel openings are voltage dependent. In the presence of micromolar luminal Ca2+, the Po and duration of sulmazole-activated openings are greater at negative voltages. However, at millimolar luminal [Ca2+], long openings are also observed at positive voltages and the Po appears to be similar at positive and negative voltages. Our findings indicate that the regulation of channel gating by luminal Ca2+ depends on the mechanism of channel activation.

摘要

我们研究了管腔[Ca2+]变化对重构于平面磷脂双分子层中的天然和纯化绵羊心脏肌浆网(SR)Ca(2+)释放通道门控的影响。仅由胞质Ca2+激活的通道,其开放概率(Po)在正的钳制电位下比负的钳制电位下更高。当管腔[Ca2+]从纳摩尔浓度增加到毫摩尔浓度时,仅由10微摩尔胞质Ca2+激活的通道在稳态Po或Po与电压的关系上没有变化。在没有激活浓度的胞质Ca2+时,通道可被磷酸二酯酶抑制剂舒马唑(AR-L 115BS)激活。然而,舒马唑对通道的非胞质Ca(2+)依赖性激活需要管腔Ca2+。在存在舒马唑的情况下,在皮摩尔管腔[Ca2+]时通道保持完全关闭。将管腔[Ca2+]增加到毫摩尔水平会通过增加开放事件的持续时间显著增加Po。舒马唑激活的、管腔Ca(2+)依赖性通道开放的Po和持续时间是电压依赖性的。在存在微摩尔管腔Ca2+时,舒马唑激活开放的Po和持续时间在负电压下更大。然而,在毫摩尔管腔[Ca2+]时,在正电压下也观察到长时间开放,并且Po在正电压和负电压下似乎相似。我们的研究结果表明,管腔Ca2+对通道门控的调节取决于通道激活机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验