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1 Istologia ed Embriologia Medica, Universita' di Roma "La Sapienza", Roma, RM, Italy
2 Medicina Sperimentale, Universita' di L'Aquila, L'Aquila, AQ, Italy
3 Anatomia e Fisiologia, Universita' di Padova, Padova, PD, Italy
* To whom correspondence should be addressed. E-mail: fabio.naro{at}uniroma1.it.
Cytoplasmic [Ca2+] ([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 increases of [Ca2+]i due to Ca2+ influx across the plasma membrane. Responses were not related to inositol-phosphate turnover and calcium 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 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 [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.
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