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

The purpose of this study was to compare the excitability and contractility of three-dimensional skeletal muscle constructs, termed myooids, engineered from C2C12 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 approximately 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 C2C12-10T1/2 cells exhibited greater rheobase, time to peak tension, and one-half relaxation time than myooids engineered from adult rodent cultures, and myooids from C2C12-10T1/2 and neonatal rat cells had greater resting baseline forces than myooids from adult rodent cultures.

[1]  H. Vandenburgh,et al.  Space travel directly induces skeletal muscle atrophy , 1999, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[2]  M S Kolodney,et al.  Isometric contraction by fibroblasts and endothelial cells in tissue culture: a quantitative study , 1992, The Journal of cell biology.

[3]  R. Close Dynamic properties of fast and slow skeletal muscles of the rat during development , 1964, The Journal of physiology.

[4]  D W James,et al.  The stress developed by sheets of chick fibroblasts in vitro. , 1969, Experimental cell research.

[5]  A. Irintchev,et al.  Ectopic skeletal muscles derived from myoblasts implanted under the skin. , 1998, Journal of cell science.

[6]  W. LaFramboise,et al.  Myosin isoforms in neonatal rat extensor digitorum longus, diaphragm, and soleus muscles. , 1990, The American journal of physiology.

[7]  Michael H. Kutner Applied Linear Statistical Models , 1974 .

[8]  H. Vandenburgh,et al.  A simplified method for tissue engineering skeletal muscle organoids in vitro , 1997, In Vitro Cellular & Developmental Biology - Animal.

[9]  H. Vandenburgh,et al.  Tissue-engineered human bioartificial muscles expressing a foreign recombinant protein for gene therapy. , 1999, Human gene therapy.

[10]  T. Matsuda,et al.  Tissue engineered skeletal muscle: preparation of highly dense, highly oriented hybrid muscular tissues. , 1998, Cell transplantation.

[11]  R. Mayne,et al.  Fibroblasts promote the formation of a continuous basal lamina during myogenesis in vitro , 1986, The Journal of cell biology.

[12]  P. V. van Wachem,et al.  Absence of muscle regeneration after implantation of a collagen matrix seeded with myoblasts. , 1999, Biomaterials.

[13]  A. Tassin,et al.  Biosynthesis of laminin and fibronectin by rat satellite cells during myogenesis in vitro. , 1985, Cell biology international reports.

[14]  H. Vandenburgh,et al.  Bioreactor perfusion system for the long-term maintenance of tissue-engineered skeletal muscle organoids , 1998, In Vitro Cellular & Developmental Biology - Animal.

[15]  N Imbert,et al.  Appearance and evolution of calcium currents and contraction during the early post-fusional stages of rat skeletal muscle cells developing in primary culture. , 1993, Development.

[16]  Cellular and molecular biology of muscle development , 2022 .

[17]  R. Simmons Cellular and molecular biology of muscle development : Edited by L.H. Kedes and F.E. Stockdale; Alan R. Liss; New York, 1989; xxxv + 1059 pages, $195.00 , 1990 .

[18]  V. Barnett,et al.  Applied Linear Statistical Models , 1975 .

[19]  Robert G. Dennis,et al.  Excitability and isometric contractile properties of mammalian skeletal muscle constructs engineered in vitro , 2000, In Vitro Cellular & Developmental Biology - Animal.

[20]  H. Vandenburgh,et al.  Attenuation of skeletal muscle wasting with recombinant human growth hormone secreted from a tissue-engineered bioartificial muscle. , 1998, Human gene therapy.

[21]  D. Turner Cell-cell and cell-matrix interactions in the morphogenesis of skeletal muscle. , 1986 .

[22]  H. Vandenburgh,et al.  Tissue-engineered skeletal muscle organoids for reversible gene therapy. , 1996, Human gene therapy.

[23]  J. S. Rao,et al.  Proteoglycan synthesis by clonal skeletal muscle cells during in vitro myogenesis: Differences detected in the types and patterns from primary cultures , 1991, International Journal of Developmental Neuroscience.

[24]  D. M. Johnston,et al.  Development of a mammalian fast muscle: dynamic and biochemical properties correlated. , 1973, The Journal of physiology.

[25]  R. Moss,et al.  Functional significance of myosin transitions in single fibers of developing soleus muscle. , 1988, The American journal of physiology.

[26]  R. Mayne,et al.  Formation of highly organized skeletal muscle fibers in vitro. Comparison with muscle development in vivo. , 1992, Journal of cell science.

[27]  R. Woledge,et al.  Neither changes in phosphorus metabolite levels nor myosin isoforms can explain the weakness in aged mouse muscle. , 1993, The Journal of physiology.

[28]  H. Vandenburgh,et al.  Computer‐aided mechanogenesis of skeletal muscle organs from single cells in vitro , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[29]  R. Close Dynamic properties of mammalian skeletal muscles. , 1972, Physiological reviews.

[30]  P. V. van Wachem,et al.  Myoblast seeding in a collagen matrix evaluated in vitro. , 1996, Journal of biomedical materials research.

[31]  J. Faulkner,et al.  Temperature-dependent physiological stability of rat skeletal muscle in vitro. , 1985, The American journal of physiology.