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J Physiol Volume 546, Number 3, 677-689, February 1, 2003 DOI: 10.1113/jphysiol.2002.027375
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J Physiol (2003), 546.3, pp. 677-689
© Copyright 2002 D 2003 The Physiological Society
DOI: 10.1113/jphysiol.2002.027375

Orthologous myosin isoforms and scaling of shortening velocity with body size in mouse, rat, rabbit and human muscles

M. A. Pellegrino, M. Canepari, R. Rossi, G. D'Antona, C. Reggiani* and R. Bottinelli

Department of Experimental Medicine, Human Physiology Unit, University of Pavia, Pavia and *Department of Anatomy and Physiology, University of Padova, Padova, Italy

Maximum shortening velocity (V0) was determined in single fibres dissected from hind limb skeletal muscles of rabbit and mouse and classified according to their myosin heavy chain (MHC) isoform composition. The values for rabbit and mouse V0 were compared with the values previously obtained in man and rat under identical experimental conditions. Significant differences in V0 were found between fibres containing corresponding myosin isoforms in different species: as a general rule for each isoform V0 decreased with body mass. Myosin isoform distributions of soleus and tibialis anterior were analysed in mouse, rat, rabbit and man: the proportion of slow myosin generally increased with increasing body size. The diversity between V0 of corresponding myosin isoforms and the different myosin isoform composition of corresponding muscles determine the scaling of shortening velocity of whole muscles with body size, which is essential for optimisation of locomotion. The speed of actin translocation (Vf) in in vitro motility assay was determined with myosins extracted from single muscle fibres of all four species: significant differences were found between myosin isoforms in each species and between corresponding myosin isoforms in different species. The values of V0 and Vf determined for each myosin isoform were significantly correlated, strongly supporting the view that the myosin isoform expressed is the major determinant of maximum shortening velocity in muscle fibres.



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