Titin-based tension in the cardiac sarcomere: Molecular origin and physiological adaptations

被引:63
作者
Anderson, Brian R. [1 ,2 ]
Granzier, Henk L. [1 ]
机构
[1] Univ Arizona, Dept Physiol, Sarver Heart Ctr, Mol Cardiovasc Res Progrum, Tucson, AZ 85724 USA
[2] Univ Arizona, Dept Phys, Tucson, AZ 85724 USA
关键词
Passive tension; Connectin; Entropic force; Mechanical signaling; MUSCLE PROTEIN TITIN; SKELETAL-MUSCLE; DILATED CARDIOMYOPATHY; PASSIVE STIFFNESS; HEART-FAILURE; HYPERTROPHIC CARDIOMYOPATHY; ISOFORM EXPRESSION; LIM PROTEIN; PEVK DOMAIN; M-LINE;
D O I
10.1016/j.pbiomolbio.2012.08.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The passive stiffness of cardiac muscle plays a critical role in ventricular filling during diastole and is determined by the extracellular matrix and the sarcomeric protein titin. Titin spans from the Z-disk to the M-band of the sarcomere and also contains a large extensible region that acts as a molecular spring and develops passive force during sarcomere stretch. This extensible segment is titin's I-band region, and its force-generating mechanical properties determine titin-based passive tension. The properties of titin's I-band region can be modulated by isoform splicing and post-translational modification and are intimately linked to diastolic function. This review discusses the physical origin of titin-based passive tension, the mechanisms that alter titin stiffness, and titin's role in stress-sensing signaling pathways. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:204 / 217
页数:14
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