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AMP-activated protein kinase is required for exercise-induced peroxisome proliferator-activated receptor co-activator 1 translocation to subsarcolemmal mitochondria in skeletal muscle.
- Source :
-
The Journal of physiology [J Physiol] 2013 Mar 15; Vol. 591 (6), pp. 1551-61. Date of Electronic Publication: 2013 Jan 07. - Publication Year :
- 2013
-
Abstract
- In skeletal muscle, mitochondria exist as two subcellular populations known as subsarcolemmal (SS) and intermyofibrillar (IMF) mitochondria. SS mitochondria preferentially respond to exercise training, suggesting divergent transcriptional control of the mitochondrial genomes. The transcriptional co-activator peroxisome proliferator-activated receptor γ co-activator 1α (PGC-1α) and mitochondrial transcription factor A (Tfam) have been implicated in the direct regulation of the mitochondrial genome in mice, although SS and IMF differences may exist, and the potential signalling events regulating the mitochondrial content of these proteins have not been elucidated. Therefore, we examined the potential for PGC-1α and Tfam to translocate to SS and IMF mitochondria in human subjects, and performed experiments in rodents to identify signalling mechanisms regulating these translocation events. Acute exercise in humans and rats increased PGC-1α content in SS but not IMF mitochondria. Acute exposure to 5-aminoimidazole-4-carboxamide-1-β-ribofuranoside in rats recapitulated the exercise effect of increased PGC-1α protein within SS mitochondria only, suggesting that AMP-activated protein kinase (AMPK) signalling is involved. In addition, rendering AMPK inactive (AMPK kinase dead mice) prevented exercise-induced PGC-1α translocation to SS mitochondria, further suggesting that AMPK plays an integral role in these translocation events. In contrast to the conserved PGC-1α translocation to SS mitochondria across species (humans, rats and mice), acute exercise only increased mitochondrial Tfam in rats. Nevertheless, in rat resting muscle PGC-1α and Tfam co-immunoprecipate with α-tubulin, suggesting a common cytosolic localization. These data suggest that exercise causes translocation of PGC-1α preferentially to SS mitochondria in an AMPK-dependent manner.
- Subjects :
- AMP-Activated Protein Kinases genetics
Animals
Cytosol metabolism
Humans
Male
Mice
Mice, Knockout
Mitochondria, Muscle classification
Muscle, Skeletal physiology
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
Physical Exertion
Protein Transport
Rats
Rats, Sprague-Dawley
Sarcolemma metabolism
Signal Transduction
Species Specificity
Trans-Activators metabolism
Young Adult
AMP-Activated Protein Kinases metabolism
Exercise
Heat-Shock Proteins metabolism
Mitochondria, Muscle metabolism
Muscle, Skeletal metabolism
RNA-Binding Proteins metabolism
Transcription Factors metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1469-7793
- Volume :
- 591
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- The Journal of physiology
- Publication Type :
- Academic Journal
- Accession number :
- 23297307
- Full Text :
- https://doi.org/10.1113/jphysiol.2012.245944