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Am J Physiol Regul Integr Comp Physiol 293: R1595-R1607, 2007. First published July 11, 2007; doi:10.1152/ajpregu.00157.2007
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NEUROHUMORAL CONTROL OF CARDIOVASCULAR FUNCTION

Interaction between myosin heavy chain and troponin isoforms modulate cardiac myofiber contractile dynamics

Murali Chandra, Matthew L. Tschirgi, Steven J. Ford, Bryan K. Slinker, and Kenneth B. Campbell

Department of Veterinary and Comparative Anatomy, Pharmacology, and Physiology, Washington State University, Pullman, Washington

Submitted 2 March 2007 ; accepted in final form 9 July 2007

Coordinated expression of species-specific myosin heavy chain (MHC) and troponin (Tn) isoforms may bring about a dynamic complementarity to match muscle contraction speed with species-specific heart rates. Contractile system function and dynamic force-length measurements were made in muscle fibers from mouse and rat hearts and in muscle fibers after reconstitution with either recombinant homologous Tn or orthologous Tn. The rate constants of length-mediated cross-bridge (XB) recruitment (b) and tension redevelopment (ktr) of mouse fibers were significantly faster than those of rat fibers. Both the tension cost (ATPase/tension) and rate constant of length-mediated XB distortion (c) were higher in the mouse than in the rat. Thus the mouse fiber was faster in all dynamic and functional aspects than the rat fiber. Mouse Tn significantly increased b and ktr in rat fibers; conversely, rat Tn significantly decreased b and ktr in mouse fibers. Thus the length-mediated recruitment of force-bearing XB occurs much more rapidly in the presence of mouse Tn than in the presence of rat Tn, demonstrating that the speed of XB recruitment is regulated by Tn. There was a significant interaction between Tn and MHC such that changes in either Tn or MHC affected the speed of XB recruitment. Our data demonstrate that the dynamics of myocardial contraction are different in the mouse and rat hearts because of sequence heterogeneity in MHC and Tn. At the myofilament level, coordinated expression of complementary regulatory contractile proteins produces a functional dynamic phenotype that allows the cardiovascular systems to function effectively at different heart rates.

myofiber dynamics; contraction speed; heart rate



Address for reprint requests and other correspondence: M. Chandra, 205 Wegner Hall, Dept. of VCAPP, Washington State Univ., WA 99164 (e-mail: murali{at}vetmed.wsu.edu)




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Cardiovasc Res, March 1, 2008; 77(4): 619 - 626.
[Abstract] [Full Text] [PDF]




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