Sodium/calcium exchange in amphibian skeletal muscle fibers and isolated transverse tubules

Author:

Cifuentes Fredy1,Vergara Julio2,Hidalgo Cecilia13

Affiliation:

1. Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Santiago 7;

2. Department of Physiology, University of California Los Angeles, Los Angeles, California 90024

3. Centro de Estudios Cientı́ficos, Valdivia, Chile; and

Abstract

The Na+/Ca2+ exchanger participates in Ca2+ homeostasis in a variety of cells and has a key role in cardiac muscle physiology. We studied in this work the exchanger of amphibian skeletal muscle, using both isolated inside-out transverse tubule vesicles and single muscle fibers. In vesicles, increasing extravesicular (intracellular) Na+ concentration cooperatively stimulated Ca2+ efflux (reverse mode), with the Hill number equal to 2.8. In contrast to the stimulation of the cardiac exchanger, increasing extravesicular (cytoplasmic) Ca2+ concentration ([Ca2+]) inhibited this reverse activity with an IC50 of 91 nM. Exchanger-mediated currents were measured at 15°C in single fibers voltage clamped at −90 mV. Photolysis of a cytoplasmic caged Ca2+ compound activated an inward current (forward mode) of 23 ± 10 nA ( n = 3), with an average current density of 0.6 μA/μF. External Na+ withdrawal generated an outward current (reverse mode) with an average current density of 0.36 ± 0.17 μA/μF ( n = 6) but produced a minimal increase in cytosolic [Ca2+]. These results suggest that, in skeletal muscle, the main function of the exchanger is to remove Ca2+ from the cells after stimulation.

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

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