Open Access
Article
Junctional membrane structure and store operated calcium entry in muscle cells
Jianjie Ma1,Zui Pan1
1
Department of Physiology and Biophysics, UMDNJ-Robert Wood Johnson Medical School, 675 Hoes Lane, Piscataway, NJ 08854, USA. maj2@umdnj.edu
DOI: 10.2741/977 Volume 8 Issue 4, pp.242-255
Published: 01 January 2003
(This article belongs to the Special Issue The structure and function of calcium release channels)
Abstract

The store-operated Ca2+ channel (SOC) located on the plasma membrane (PM) mediates capacitative entry of extracellular Ca2+ following depletion of intracellular Ca2+ stores in the endoplasmic or sarcoplasmic reticulum (ER/SR). It plays important roles in a variety of cell signaling processes, including proliferation, apoptosis, gene regulation and motility. In skeletal muscle, the L-type Ca2+ channel on the surface membrane has slow kinetics of activation in response to voltage stimulation, and therefore does not support entry of extracellular Ca2+. Recent studies have provided functional evidence for the existence of SOC in muscle cells. Severe dysfunction of SOC is identified in muscle cells lacking either ryanodine receptors located on the SR membrane, or mitsugumin 29 - a membrane protein located in the triad junction of skeletal muscle. These results indicate that SOC activation requires an intact interaction between PM and SR, and is linked to conformational changes of ryanodine receptors. The cumulative entry of Ca2+ through SOC not only provides the mechanism for refilling of intracellular Ca2+ stores, but may also add to the Ca2+ needed for muscle contraction under conditions of intensive exercise and fatigue. The proper coupling of PM with ER/SR, in the triad junction in skeletal muscle or dyad junction in cardiac muscle, is essential not only for the membrane excitation-induced intracellular Ca2+ release but also for the store depletion-initiated capacitative Ca2+ entry.

Share and Cite
Jianjie Ma, Zui Pan. Junctional membrane structure and store operated calcium entry in muscle cells. Frontiers in Bioscience-Landmark. 2003. 8(4); 242-255.