Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress

1 In Duchenne muscular dystrophy (DMD) dysregulation of cytosolic calcium appears to be involved in the degeneration of skeletal muscle fibres. Therefore, we have studied the regulation of the free cytosolic calcium concentration ([Ca2+](c)) under specific stress conditions in cultured myotubes isolated from the hind limbs of wild-type (C57BL10) and dystrophin-deficient mutant mdx mice. [Ca2+](c) in the myotubes was estimated by the use of the Ca2+-sensitive fluorescent dye, fura-2. 2 Resting [Ca2+](c) was similar in mdx and normal myotubes (35+/-9 nM and 38+/-11 nM, respectively). However, when mdx myotubes were exposed to a high extracellular calcium concentration ([Ca2+](e)) of 40 mM, the [Ca2+](c) was elevated to 84+/-29 nM, compared to 49+/-7 nM in normal myotubes. 3 Lowering the osmolarity of the superfusion solution from 300 mOsm to 100 mOsm resulted also in a rise in [Ca2+](c) which was about two times higher for mdx (243+/-65 nM) than for C57BL10 (135+/-37 nM). Replacing extracellular Ca2+ by EGTA (0.2 mM) prevented the rise in [Ca2+](c) in both mdx and normal myotubes when exposed to the low osmolarity solution. 4 Gadolinium ion (50 mu M), an inhibitor of Ca2+ entry, antagonized the rise in [Ca2+](e) of myotubes superfused with 40 mM [Ca2+](e) by 20-40% for both mdx and C57BL10 cells, but did not significantly reduce the rise in [Ca2+](c) when the cells were exposed to the hypo-osmotic buffer (100 mOsm). 5 Incubation of the cell culture for 3-5 days from the onset of induction of myotube formation with the membrane permeable protease inhibitor, calpeptin (50 mu M) abolished the rise in [Ca2+](c) in mdx myotubes upon exposure to hypo-osmotic shock. 6 Treatment of the cell culture for 3-5 days with alpha-methylprednisolone (PDN, 10 mu M) attenuated the rise in [Ca2+](c) following hypo-osmotic stress for both normal and mdx myotubes by about 50%. 7 The results described here suggest an increased permeability of mdx myotubes to Ca2+ under specific stress conditions. The ameliorating effect of PDN on [Ca2+](c) could explain, at least partly, the beneficial effect of this drug on DMD patients.