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J Physiol ; 541(Pt 3): 835-47, 2002 Jun 15.
Article in English | MEDLINE | ID: mdl-12068044

ABSTRACT

Contractile activity imposed by chronic electrical stimulation of a primary skeletal muscle cell culture grown on microcarriers over several days led to an increase of slow myosin heavy chain I (MHCI) and a decrease of fast MHCII expression at mRNA and protein levels, indicating an ongoing fast-to-slow transformation. Only patterns with periods of continuous stimulation of > or = 5 min in a 45 min cycle were capable of inducing a fibre type transformation, and this was independent of the applied stimulation frequency over the range 1-10 Hz. We have shown before that the calcineurin-NFATc1 signalling pathway is indispensable in mediating MHCI upregulation during fibre type transformation. Therefore, subcellular localization of NFATc1 was studied immunocytochemically. This revealed that only one stimulation train lasting for > or = 5 min was sufficient to induce nuclear import of this factor, which was about complete after 20 min of continuous stimulation. For both induction of NFATc1 import and MHCI mRNA upregulation, the minimum stimulation interval of > or = 5 min was sufficient and stimulation frequency was not crucial between 1 and 10 Hz. Repetition of stimulation cycles, with pauses (40 min) shorter than the time required for complete export of NFATc1, led to an accumulation of NFATc1 in the nuclei with each cycle and thus to an amplification of the transformation signal during extended periods of electrostimulation. The temporal behaviour of NFATc import/export appears to determine the effectiveness of various electrostimulation protocols in inducing fast-to-slow fibre transformation.


Subject(s)
Cell Nucleus/metabolism , DNA-Binding Proteins/metabolism , Muscle Fibers, Fast-Twitch/physiology , Muscle Fibers, Slow-Twitch/physiology , Muscle, Skeletal/metabolism , Nuclear Proteins , Transcription Factors/metabolism , Animals , Animals, Newborn , Blotting, Northern , Cells, Cultured , Electric Stimulation , Electrophoresis, Polyacrylamide Gel , Fluorescent Antibody Technique , Isomerism , Kinetics , Membrane Potentials/physiology , Muscle, Skeletal/cytology , Myosin Heavy Chains/chemistry , Myosin Heavy Chains/metabolism , NFATC Transcription Factors , Rabbits
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