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1 Dipartimento di Istologia ed Embriologia Medica, Università "La Sapienza," 00161 Rome; 2 Dipartimento di Medicina Sperimentale, Università di L'Aquila, 60710 L'Aquila; and 3 Dipartimento di Anatomia e Fisiologia, Università di Padova, 35131 Padua, Italy
Cytoplasmic Ca2+ concentration ([Ca2+]i) variation is a key event in myoblast differentiation, but the mechanism by which it occurs is still debated. Here we show that increases of extracellular Ca2+ concentration ([Ca2+]o) produced membrane hyperpolarization and a concentration-dependent increase of [Ca2+]i due to Ca2+ influx across the plasma membrane. Responses were not related to inositol phosphate turnover and Ca2+-sensing receptor. [Ca2+]o-induced [Ca2+]i increase was inhibited by Ca2+ channel inhibitors and appeared to be modulated by several kinase activities. [Ca2+]i increase was potentiated by depletion of intracellular Ca2+ stores and depressed by inactivation of the Na+/Ca2+ exchanger. The response to arginine vasopressin (AVP), which induces inositol 1,4,5-trisphosphate-dependent [Ca2+]i increase in L6-C5 cells, was not modified by high [Ca2+]o. On the contrary, AVP potentiated the [Ca2+]i increase in the presence of elevated [Ca2+]o. Other clones of the L6 line as well as the rhabdomyosarcoma RD cell line and the satellite cell-derived C2-C12 line expressed similar responses to high [Ca2+]o, and the amplitude of the responses was correlated with the myogenic potential of the cells.
calcium; myogenesis; calcium channels; sodium-calcium exchanger
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B. Fioretti, T. Pietrangelo, L. Catacuzzeno, and F. Franciolini Intermediate-conductance Ca2+-activated K+ channel is expressed in C2C12 myoblasts and is downregulated during myogenesis Am J Physiol Cell Physiol, July 1, 2005; 289(1): C89 - C96. [Abstract] [Full Text] [PDF] |
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