Abstract
Muscular dysgenesis (mdg) is a spontaneous recessive lethal mutation in the mouse. The disease is characterized by a total lack of excitation-contraction coupling in embryonic skeletal muscle1–4. This developmental abnormality is associated with a drastic deficiency in the expression of voltage-sensitive Ca2+ channels in skeletal muscle3–5 without alteration of the properties of voltage-sensitive Na+ channels4 or of voltage-sensitive Ca2+ channels in cardiac3,5 and neuronal cells5. Membrane couplings between sarcoplasmic reticulum and the transverse tubules, known as triads, were also found to be drastically altered in embryonic muscle of the homozygous mutant (mdg / mdg). Triads in the mdg/mdg muscle were less numerous, disorganized and lacked spaced densities3,6. This paper shows that co-culture of mdg/mdg myotubes with normal spinal cord neurons re-establishes Ca2+ channel activity, contraction and normal triad organization. The decrease thus cannot be due to a mutation of the Ca2+ channel as previously suggested5. Normal nerve cells may supply an essential factor to mutant muscle cells.
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1. Bowden-Essien, F. Devl Biol. 27, 351–364 (1972). 2. Koenig, J., Bournaud, R., Powell, J. A. & Rieger, F. Devl Biol. 92, 188–196 (1982). 3. Pitmen-Raymond, M., Rieger, F., Fosset, M.& Lazdunski, M. Devl Biol. 112,458–466(1985). 4. Romey, G., Rieger, F., Renaud, J. F., Pin9on-Raymond, M. & Lazdunski, M. Biochem. biophys. Res. Commun. 136, 935–940 (1986). 5. Beam, K. G., Knudson, C. M. & Powell, J. A. Nature 320, 168–170 (1986). 6. Banker, B. M. J. Neuropath, exp. Neurol. 36, 100–127 (1977). 7. Bordes, M., Bernengo, J. C. & Renaud, J. F. Rev. sclent. Instrum. 54, 1053–1058 (1983). 8. Hugues, M. et al. EMBO J. 1, 1039–1042 (1982). 9. Romey, G. & Lazdunski, M. Biochem. biophys. Res. Commun. 118, 669–674 (1984). 10. Cohen, M. W. Brain Res. 41, 457–463 (1972). 11. Cognard, C., Lazdunski, M. & Romey, G. Proc. natn. Acad. Sci. U.S.A. 83, 517–521 (1986). 12. Carbone, E. & Lux, H. D. Nature 310, 501–502 (1984). 13. Nowycky, M. C., Fox, A. P. & Tsien, R. W. Nature 316, 440–442 (1985). 14. Nilius, B., Hess, P., Lansman, J. B. & Tsien, R. W. Nature 316, 443–446 (1985). 15. Bossu, J. L., Feltz, A. & Thomann, J. M. Pfliigers Arch. ges. Physiol. 403, 360–368 (1985). 16. Bean, B. P. J. gen. Physiol. 86, 1–30 (1985). 17. Hamill, P., Marty, A., Neher, E., Sakman, B. & Sigworth, F. J. Pfliigers Arch. ges. Physiol. 391,85–100 (1981). 18. Pincon-Raymond, M., Murawsky, M., Mege, R. M. & Rieger, F. Devl Biol. (in the press).
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Rieger, F., Bournaud, R., Shimahara, T. et al. Restoration of dysgenic muscle contraction and calcium channel function by co-culture with normal spinal cord neurons. Nature 330, 563–566 (1987). https://doi.org/10.1038/330563a0
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DOI: https://doi.org/10.1038/330563a0
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