Excitability and contractility of skeletal muscle engineered from primary cultures and cell lines

1  Muscle Mechanics Laboratory, Institute of Gerontology, University of Michigan, Ann Arbor 48109-2007; and 2  Gilbert Engineering, Inc., Ann Arbor, Michigan 48103-9005 The purpose of this study was to compare the excitability and contractility of three-dimensional skeletal muscle constructs, termed...

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Veröffentlicht in:American Journal of Physiology: Cell Physiology 2001-02, Vol.280 (2), p.C288-C295
Hauptverfasser: Dennis, Robert G, Kosnik, Paul E., II, Gilbert, Mark E, Faulkner, John A
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Sprache:eng
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Zusammenfassung:1  Muscle Mechanics Laboratory, Institute of Gerontology, University of Michigan, Ann Arbor 48109-2007; and 2  Gilbert Engineering, Inc., Ann Arbor, Michigan 48103-9005 The purpose of this study was to compare the excitability and contractility of three-dimensional skeletal muscle constructs, termed myooids, engineered from C 2 C 12 myoblast and 10T1/2 fibroblast cell lines, primary muscle cultures from adult C3H mice, and neonatal and adult Sprague-Dawley rats. Myooids were 12 mm long, with diameters of 0.1-1 mm, were excitable by transverse electrical stimulation, and contracted to produce force. After ~30 days in culture, myooid cross-sectional area, rheobase, chronaxie, resting baseline force, twitch force, time to peak tension, one-half relaxation time, and peak isometric force were measured. Specific force was calculated by dividing peak isometric force by cross-sectional area. The specific force generated by the myooids was 2-8% of that generated by skeletal muscles of control adult rodents. Myooids engineered from C 2 C 12 -10T1/2 cells exhibited greater rheobase, time to peak tension, and one-half relaxation time than myooids engineered from adult rodent cultures, and myooids from C 2 C 12 -10T1/2 and neonatal rat cells had greater resting baseline forces than myooids from adult rodent cultures. tissue engineering; myooid; myogenesis; isometric force; rodent tissue culture
ISSN:0363-6143
1522-1563
DOI:10.1152/ajpcell.2001.280.2.c288