Fujita Hideaki, Labeit Dietmar, Gerull Brenda, Labeit Siegfried, Granzier Henk L
Dept. of Veterinary and Comparative Anatomy, Pharmacology, and Physiology, Washington State Univ., Pullman, WA 99164, USA.
Am J Physiol Heart Circ Physiol. 2004 Dec;287(6):H2528-34. doi: 10.1152/ajpheart.00553.2004.
We studied the effects of Ca2+ on titin (connectin)-based passive tension in skinned myocardium expressing either predominantly N2B titin (rat right ventricle, RRV) or predominantly N2BA titin (bovine left atrium, BLA). Actomyosin-based tension was abolished to undetectably low levels by selectively removing the thin filaments with a Ca2+-insensitive gelsolin fragment (FX-45). Myocardium was stretched in the presence and absence of Ca2+, and passive tension was measured. Ca2+ significantly increased passive tension during and after stretch in the BLA. The increase was insensitive to the actomyosin inhibitor 2,3-butanedione 2-monoxime, supporting the conclusion that the effect is titin based. Passive tension did not respond to calcium in the RRV, indicating that passive tension developed by N2B titin is calcium insensitive. Western blot analysis and immunofluorescence studies indicated that N2BA titin expresses E-rich PEVK motifs, whereas they are absent from N2B titin, supporting earlier single molecule studies that reported that E-rich motifs are required for calcium sensitivity. We conclude that calcium affects passive myocardial tension in a titin isoform-dependent manner.
我们研究了钙离子对表达主要为N2B肌联蛋白(大鼠右心室,RRV)或主要为N2BA肌联蛋白(牛左心房,BLA)的去表皮心肌中基于肌联蛋白(连接蛋白)的被动张力的影响。通过用对钙离子不敏感的凝溶胶蛋白片段(FX - 45)选择性去除细肌丝,将基于肌动球蛋白的张力消除到无法检测到的低水平。在有钙离子和无钙离子的情况下对心肌进行拉伸,并测量被动张力。钙离子显著增加了BLA拉伸期间和拉伸后的被动张力。这种增加对肌动球蛋白抑制剂2,3 - 丁二酮单肟不敏感,支持了该效应基于肌联蛋白的结论。RRV中的被动张力对钙离子无反应,表明由N2B肌联蛋白产生的被动张力对钙离子不敏感。蛋白质免疫印迹分析和免疫荧光研究表明,N2BA肌联蛋白表达富含E的PEVK基序,而N2B肌联蛋白中不存在这些基序,这支持了早期的单分子研究报告,即富含E的基序是钙离子敏感性所必需的。我们得出结论,钙离子以肌联蛋白异构体依赖性方式影响心肌被动张力。