Research Paper Volume 3, Issue 6 pp 621—634
Store-Operated Ca2+ Entry (SOCE) Contributes to Normal Skeletal Muscle Contractility in young but not in aged skeletal muscle
- 1 Department of Physiology & Biophysics, Robert Wood Johnson Medical School and
- 2 Rutgers University Physiology and Integrative Biology and Department of Biomedical Engineering, Piscataway, New Jersey, 08854
- 3 The Muscle Biology Research Group-MUBIG, Schools of Nursing and Medicine, University of Missouri-Kansas City, Missouri, Kansas City, Missouri, 64108
- 4 Departments of Anesthesiology and Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine and Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, 15122
- 5 Department of Physiology & Biophysics, Case Western Reserve University, Cleveland, Ohio, 44106
- 6 Department of Physiology & Biophysics, University of Kentucky, Lexington, Kentucky, 40504
- 7 In Memoriam of Brian Hardin
Received: May 30, 2011 Accepted: June 4, 2011 Published: June 6, 2011
https://doi.org/10.18632/aging.100335How to Cite
Abstract
Muscle atrophy alone is insufficient to explain the significant decline in contractile force of skeletal muscle during normal aging. One contributing factor to decreased contractile force in aging skeletal muscle could be compromised excitation-contraction (E-C) coupling, without sufficient available Ca2+ to allow for repetitive muscle contractility, skeletal muscles naturally become weaker. Using biophysical approaches, we previously showed that store-operated Ca2+ entry (SOCE) is compromised in aged skeletal muscle but not in young ones. While important, a missing component from previous studies is whether or not SOCE function correlates with contractile function during aging. Here we test the contribution of extracellular Ca2+ to contractile function of skeletal muscle during aging. First, we demonstrate graded coupling between SR Ca2+ release channel-mediated Ca2+ release and activation of SOCE. Inhibition of SOCE produced significant reduction of contractile force in young skeletal muscle, particularly at high frequency stimulation, and such effects were completely absent in aged skeletal muscle. Our data indicate that SOCE contributes to the normal physiological contractile response of young healthy skeletal muscle and that defective extracellular Ca2+ entry through SOCE contributes to the reduced contractile force characteristic of aged skeletal muscle.