Myofilament length dependent activation

被引:217
作者
de Tombe, Pieter P. [1 ]
Mateja, Ryan D. [1 ]
Tachampa, Kittipong [1 ]
Mou, Younss Ait [1 ]
Farman, Gerrie P. [1 ]
Irving, Thomas C. [2 ,3 ]
机构
[1] Loyola Univ, Stritch Sch Med, Dept Cell & Mol Physiol, Maywood, IL 60153 USA
[2] IIT, CSRRI, Chicago, IL 60616 USA
[3] IIT, Dept Biol Chem & Phys Sci, Chicago, IL 60616 USA
基金
美国国家卫生研究院;
关键词
Frank-Starling Law of The Heart; Length-Tension Relationship; Sarcomere length; Regulation; RABBIT SKELETAL-MUSCLE; X-RAY-DIFFRACTION; REGULATORY UNIT INTERACTIONS; THIN FILAMENT ACTIVATION; SKINNED CARDIAC-MUSCLE; MYOFIBRILLAR ADENOSINE-TRIPHOSPHATASE; FORCE REDEVELOPMENT KINETICS; FRANK-STARLING RELATIONSHIP; MAGNESIUM BINDING-SITES; GIANT PROTEIN TITIN;
D O I
10.1016/j.yjmcc.2009.12.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Frank-Starling law of the heart describes the interrelationship between end-diastolic volume and cardiac ejection volume, a regulatory system that operates on a beat-to-beat basis. The main cellular mechanism that underlies this phenomenon is an increase in the responsiveness of cardiac myofilaments to activating Ca2+ ions at a longer sarcomere length, commonly referred to as myofilament length-dependent activation. This review focuses on what molecular mechanisms may underlie myofilament length dependency. Specifically, the roles of inter-filament spacing, thick and thin filament based regulation, as well as sarcomeric regulatory proteins are discussed. Although the "Frank-Starling law of the heart" constitutes a fundamental cardiac property that has been appreciated for well over a century, it is still not known in muscle how the contractile apparatus transduces the information concerning sarcomere length to modulate ventricular pressure development. (C) 2009 Elsevier Ltd. All rights reserved.
引用
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页码:851 / 858
页数:8
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