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Publication : Inverse regulation of the cytosolic Ca²⁺ buffer parvalbumin and mitochondrial volume in muscle cells via SIRT1/PGC-1α axis.

First Author  Ducreux S Year  2012
Journal  PLoS One Volume  7
Issue  9 Pages  e44837
PubMed ID  23028640 Mgi Jnum  J:191868
Mgi Id  MGI:5463506 Doi  10.1371/journal.pone.0044837
Citation  Ducreux S, et al. (2012) Inverse regulation of the cytosolic Ca(2)(+) buffer parvalbumin and mitochondrial volume in muscle cells via SIRT1/PGC-1alpha axis. PLoS One 7(9):e44837
abstractText  Skeletal muscles show a high plasticity to cope with various physiological demands. Different muscle types can be distinguished by the force, endurance, contraction/relaxation kinetics (fast-twitch vs. slow-twitch muscles), oxidative/glycolytic capacity, and also with respect to Ca(2)(+)-signaling components. Changes in Ca(2)(+) signaling and associated Ca(2)(+)-dependent processes are thought to underlie the high adaptive capacity of muscle fibers. Here we investigated the consequences and the involved mechanisms caused by the ectopic expression of the Ca(2)(+)-binding protein parvalbumin (PV) in C2C12 myotubes in vitro, and conversely, the effects caused by its absence in in fast-twitch muscles of parvalbumin null-mutant (PV(-)/(-)) mice in vivo. The absence of PV in fast-twitch muscle tibialis anterior (TA) resulted in an increase in the peroxisome proliferator-activated receptor gamma coactivator 1alpha (PGC-1alpha) and of its positive regulator, the deacetylase sirtuin 1 (SIRT1). TA muscles from PV(-)/(-) mice also have an increased mitochondrial volume. Mild ionophore treatment of control (PV-devoid) C2C12 myotubes causing a moderate elevation in [Ca(2)(+)](c) resulted in an increase in mitochondrial volume, together with elevated PGC-1alpha and SIRT1 expression levels, whilst it increased PV expression levels in myotubes stably transfected with PV. In PV-expressing myotubes the mitochondrial volume, PGC-1alpha and SIRT1 were significantly lower than in control C2C12 myotubes already at basal conditions and application of ionophore had no effect on either one. SIRT1 activation causes a down-regulation of PV in transfected myotubes, whilst SIRT1 inhibition has the opposite effect. We conclude that PV expression and mitochondrial volume in muscle cells are inversely regulated via a SIRT1/PGC-1alpha signaling axis.
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