Suppr超能文献

钒酸钠对心肌中横桥结合、力重建及Ca2+激活的力抑制作用。

The effects of force inhibition by sodium vanadate on cross-bridge binding, force redevelopment, and Ca2+ activation in cardiac muscle.

作者信息

Martyn D A, Smith L, Kreutziger K L, Xu S, Yu L C, Regnier M

机构信息

Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.

出版信息

Biophys J. 2007 Jun 15;92(12):4379-90. doi: 10.1529/biophysj.106.096768. Epub 2007 Mar 30.

Abstract

Strongly bound, force-generating myosin cross-bridges play an important role as allosteric activators of cardiac thin filaments. Sodium vanadate (Vi) is a phosphate analog that inhibits force by preventing cross-bridge transition into force-producing states. This study characterizes the mechanical state of cross-bridges with bound Vi as a tool to examine the contribution of cross-bridges to cardiac contractile activation. The K(i) of force inhibition by Vi was approximately 40 microM. Sinusoidal stiffness was inhibited with Vi, although to a lesser extent than force. We used chord stiffness measurements to monitor Vi-induced changes in cross-bridge attachment/detachment kinetics at saturating [Ca(2+)]. Vi decreased chord stiffness at the fastest rates of stretch, whereas at slow rates chord stiffness actually increased. This suggests a shift in cross-bridge population toward low force states with very slow attachment/detachment kinetics. Low angle x-ray diffraction measurements indicate that with Vi cross-bridge mass shifted away from thin filaments, implying decreased cross-bridge/thin filament interaction. The combined x-ray and mechanical data suggest at least two cross-bridge populations with Vi; one characteristic of normal cycling cross-bridges, and a population of weak-binding cross-bridges with bound Vi and slow attachment/detachment kinetics. The Ca(2+) sensitivity of force (pCa(50)) and force redevelopment kinetics (k(TR)) were measured to study the effects of Vi on contractile activation. When maximal force was inhibited by 40% with Vi pCa(50) decreased, but greater force inhibition at higher [Vi] did not further alter pCa(50). In contrast, the Ca(2+) sensitivity of k(TR) was unaffected by Vi. Interestingly, when force was inhibited by Vi k(TR) increased at submaximal levels of Ca(2+)-activated force. Additionally, k(TR) is faster at saturating Ca(2+) at [Vi] that inhibit force by > approximately 70%. The effects of Vi on k(TR) imply that k(TR) is determined not only by the intrinsic properties of the cross-bridge cycle, but also by cross-bridge contribution to thin filament activation.

摘要

紧密结合、产生力量的肌球蛋白横桥作为心脏细肌丝的变构激活剂发挥着重要作用。钒酸钠(Vi)是一种磷酸类似物,它通过阻止横桥转变为产生力量的状态来抑制力量。本研究将结合Vi的横桥的力学状态作为一种工具来表征横桥对心脏收缩激活的贡献。Vi对力量抑制的K(i)约为40 microM。正弦刚度受到Vi的抑制,尽管程度小于力量。我们使用弦刚度测量来监测在饱和[Ca(2+)]时Vi诱导的横桥附着/脱离动力学变化。Vi在最快拉伸速率下降低弦刚度,而在慢速时弦刚度实际上增加。这表明横桥群体向具有非常缓慢附着/脱离动力学的低力量状态转变。低角度X射线衍射测量表明,存在Vi时横桥质量从细肌丝移开,这意味着横桥/细肌丝相互作用减少。X射线和力学数据相结合表明,存在Vi时至少有两种横桥群体;一种是正常循环横桥的特征,另一种是结合Vi且附着/脱离动力学缓慢的弱结合横桥群体。测量了力量的Ca(2+)敏感性(pCa(50))和力量再发展动力学(k(TR))以研究Vi对收缩激活的影响。当最大力量被Vi抑制40%时,pCa(50)降低,但在更高[Vi]下更大的力量抑制并未进一步改变pCa(50)。相比之下,k(TR)的Ca(2+)敏感性不受Vi影响。有趣的是,当力量被Vi抑制时,在亚最大水平的Ca(2+)激活力量下k(TR)增加。此外,在抑制力量>约70%的[Vi]下,饱和Ca(2+)时k(TR)更快。Vi对k(TR)的影响意味着k(TR)不仅由横桥循环的内在特性决定,还由横桥对细肌丝激活的贡献决定。

相似文献

引用本文的文献

本文引用的文献

6
Single particle analysis of relaxed and activated muscle thin filaments.松弛和激活状态下肌肉细肌丝的单颗粒分析
J Mol Biol. 2005 Feb 25;346(3):761-72. doi: 10.1016/j.jmb.2004.12.013. Epub 2005 Jan 11.

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