Temporal Expression of Calcium Channel Subunits in Satellite Cells and Bone Marrow Mesenchymal Cells

Bone marrow-derived mesenchymal stem cells (MSC) can be differentiated into myocytes, as well as adipocytes, chondrocytes, and osteocytes in culture. Calcium channels mediate excitation-contraction coupling and are essential for the function of muscle. However, little is known about the expression o...

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Veröffentlicht in:Stem cell reviews 2015-06, Vol.11 (3), p.408-422
Hauptverfasser: Grajales, Liliana, Lach, Lawrence E., Janisch, Patrick, Geenen, David L., García, Jesús
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Sprache:eng
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Zusammenfassung:Bone marrow-derived mesenchymal stem cells (MSC) can be differentiated into myocytes, as well as adipocytes, chondrocytes, and osteocytes in culture. Calcium channels mediate excitation-contraction coupling and are essential for the function of muscle. However, little is known about the expression of calcium channel subunits and calcium handling in stem cells. We examined whether the expression of calcium channel subunits in MSC is similar to that of skeletal muscle satellite cells and if their levels of expression are modified after treatment with bone morphogenetic protein-4 (BMP4). We found that during myogenic differentiation, MSC first express the α2δ1 subunit and the cardiac channel subunit Ca v 1.2. In contrast to the α2δ1 subunit levels, the Ca v 1.2 subunit decreases rapidly with time. The skeletal channel subunit Ca v 1.1 is detected at day 3 but its expression increases considerably, resembling more closely the expression of the subunits in satellite cells. Treatment of MSC with BMP4 caused a significant increase in expression of Ca v 1.2, a delay in expression of Ca v 1.1, and a reduction in the duration of calcium transients when extracellular calcium was removed. Calcium currents and transients followed a pattern related to the expression of the cardiac (Ca v 1.2) or skeletal (Ca v 1.1) α1subunits. These results indicate that differentiation of untreated MSC resembles differentiation of skeletal muscle and that BMP4 reduces skeletal muscle calcium channel expression and promotes the expression of cardiac calcium channels during myogenic differentiation.
ISSN:1550-8943
2629-3269
1558-6804
2629-3277
DOI:10.1007/s12015-014-9566-4