Cardiac titin isoforms are coexpressed in the half-sarcomere and extend independently

被引:74
作者
Trombitás, K
Wu, Y
Labeit, D
Labeit, S
Granzier, H [1 ]
机构
[1] Washington State Univ, Pullman, WA 99164 USA
[2] Univ Hosp Mannheim, D-68135 Mannheim, Germany
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2001年 / 281卷 / 04期
关键词
diastole; elasticity; structure; mechanics; physiology;
D O I
10.1152/ajpheart.2001.281.4.H1793
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Titin, the third myofilament type of cardiac muscle, contains a molecular spring segment that gives rise to passive forces in stretched myocardium and to restoring forces in shortened myocardium. We studied cardiac titin isoforms (N2B and N2BA) that contain length variants of the molecular spring segment. We investigated how coexpression of isoforms takes place at the level of the half-sarcomere, and whether coexpression affects the extensibility of the isoforms. Immunoelectron microscopy was used to study local coexpression of isoforms in a range of species. It was found that the cardiac sarcomere of large mammals coexpresses N2B and N2BA titin isoforms at the level of the half-sarcomere, and that when coexpressed, the isoforms act independently of one another. Coexpressing isoforms at varying ratios results in modulation of the passive mechanical behavior of the sarcomere without impacting other functions of titin and allows for adjustment of the diastolic properties of the myocardium.
引用
收藏
页码:H1793 / H1799
页数:7
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