In this study we investigated the role of extracellular 5' guanosine-triphosphate (GTP) on early phases of skeletal muscle differentiation using the widely used C2C12 mouse cells as a myogenic model. We show that extracellular GTP binding to specific sites activates a metabotropic cascade that leads to a transient intracellular Ca2+ mobilization, consequent activation of the intermediate Ca2+ -activated K+ channels (IKCa), and hyperpolarization of the plasma membrane.We further show that in differentiating C2C12 myoblasts GTP induces a proliferative boost, and increases the number of cells positive for the myosin heavy chain (MyHC) proteins. These effects were shown to be mediated by the IKCa channel-dependent hyperpolarization, as evidenced by their disappearance when myoblasts were incubatedwith theIKCa channel inhibitor charybdotoxin. These data give new insights into nucleotide purinergic signalling pathways, and address the role of the GTP-dependent IKCa channel activation and hyperpolarization in myogenesis.
Extracellular guanosine-5'triphosphate modulates myogenesis via intermediate Ca2+-activated K+ currents on C2C12 mouse cells
PIETRANGELO, Tiziana;MANCINELLI, Rosa;FANO' ILLIC', Giorgio;FULLE, Stefania
2006-01-01
Abstract
In this study we investigated the role of extracellular 5' guanosine-triphosphate (GTP) on early phases of skeletal muscle differentiation using the widely used C2C12 mouse cells as a myogenic model. We show that extracellular GTP binding to specific sites activates a metabotropic cascade that leads to a transient intracellular Ca2+ mobilization, consequent activation of the intermediate Ca2+ -activated K+ channels (IKCa), and hyperpolarization of the plasma membrane.We further show that in differentiating C2C12 myoblasts GTP induces a proliferative boost, and increases the number of cells positive for the myosin heavy chain (MyHC) proteins. These effects were shown to be mediated by the IKCa channel-dependent hyperpolarization, as evidenced by their disappearance when myoblasts were incubatedwith theIKCa channel inhibitor charybdotoxin. These data give new insights into nucleotide purinergic signalling pathways, and address the role of the GTP-dependent IKCa channel activation and hyperpolarization in myogenesis.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.