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Damage to developing mouse skeletal muscle myotubes in culture: protective effect of heat shock proteins
Author(s) -
Maglara A. A.,
Vasilaki A.,
Jackson M. J.,
McArdle A.
Publication year - 2003
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.2003.00837.x
Subject(s) - pacemaker potential , anatomy , skeletal muscle , syncytium , chemistry , myogenesis , electrophysiology , ion channel , peristalsis , biology , medicine , microbiology and biotechnology , neuroscience , receptor , cell , biochemistry
Damage to skeletal muscle occurs following excessive exercise, upon reperfusion following ischaemia and in disease states, such as muscular dystrophy. Key mechanisms by which damage is thought to occur include a loss of intracellular calcium homeostasis, loss of energy supply to the cell, increased activity of oxidising free radical‐mediated reactions and activation of apoptosis pathways. An increased cellular content of heat shock proteins (HSPs) has been shown to protect skeletal muscle against some forms of damage, although the mechanistic basis of this protection is not clearly understood. The aim of this study was to establish a cell culture‐based model of damage to C 2 C 12 skeletal muscle cells using the calcium ionophore, A23187 and the mitochondrial uncoupler, 2,4‐dinitrophenol (DNP) as damaging agents. Treatment of cells with 1 m m DNP for 60 min resulted in the release of 63.5 % of intracellular creatine kinase (CK) activity over the 3 h experimental period. Treatment of cells with 10 μ m A23187 for 30 min resulted in the release of 47.9 % of CK activity. Exposure of myotubes to a period of hyperthermia resulted in a significant increase in their content of HSP25, HSP60, HSC70 (heat shock cognate) and HSP70. This increase in HSPs was associated with significant protection against both DNP‐induced and A23187‐induced damage to the myotubes. These results indicate that an increased content of HSPs may provide protection against the muscle damage that occurs by a pathological increase in intracellular calcium or uncoupling of the mitochondrial respiratory chain.