Key result
Skeletal myoblast transplantation down-regulates voltage-gated ion channels in infarcted rat myocardium within two weeks.
Why the study?
The effect of the infarcted myocardial environment on voltage-gated ion channel expression in transplanted skeletal muscle myoblasts was unclear.
The infarcted myocardial environment causes significant down-regulation of voltage-gated ion channels in transplanted skeletal myoblasts, potentially affecting their electrophysiological integration.
Answers are grounded in this paper and cite their sources.
May hinder myoblast electrophysiological integration post-infarct; leaves open ion channel modulation to improve cell therapy outcomes.
We have analysed the voltage-gated ion channels and fusion competence of skeletal muscle myoblasts labelled with green fluorescent protein (GFP) and the membrane dye PKH transplanted into the infarcted myocardium of syngenic rats. After cell transplantation the animals were killed and GFP(+)-PKH(+) myoblasts enzymatically isolated for subsequent studies of ionic currents through voltage-gated sodium, calcium and potassium channels. A down-regulation of all three types of ion channels after engraftment was observed. The fraction of cells with calcium (68%) and sodium channels (65%) declined to zero within 24 h and 1 week, respectively. Down-regulation of potassium currents (90% in control) occurred within 2 weeks to about 30%. Before injection myoblasts expressed predominantly transient outward potassium channels whereas after isolation from the myocardium exclusively rapid delayed rectifier channels. The currents recovered completely between 1 and 6 weeks under cell culture conditions. The down-regulation of ion channels and changes in potassium current kinetics suggest that the environment provided by infarcted myocardium affects expression of voltage-gated ion channels of skeletal myoblasts.
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Ott et al. (2004) studied infarcted myocardium. skeletal muscle myoblast transplantation vs. pre-injection/control myoblasts was evaluated on expression of voltage-gated ion channels. Transplantation of skeletal myoblasts into infarcted rat myocardium resulted in the down-regulation of voltage-gated calcium, sodium, and potassium channels within 1 to 2 weeks.
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