Presented at the AuPS (AHMRC) Symposium Integrative Aspects of Human Muscle Performance, November 2004. The papers in these proceedings were peer reviewed under the supervision of the AuPS editor. The papers are being published with the permission of AuPS and were initially published on the AuPS website http://www.aups.org.au.
EXERCISE AND SKELETAL MUSCLE GLUCOSE TRANSPORTER 4 EXPRESSION: MOLECULAR MECHANISMS
Article first published online: 16 MAR 2006
Clinical and Experimental Pharmacology and Physiology
Volume 33, Issue 4, pages 395–399, April 2006
How to Cite
McGee, S. L. and Hargreaves, M. (2006), EXERCISE AND SKELETAL MUSCLE GLUCOSE TRANSPORTER 4 EXPRESSION: MOLECULAR MECHANISMS. Clinical and Experimental Pharmacology and Physiology, 33: 395–399. doi: 10.1111/j.1440-1681.2006.04362.x
- Issue published online: 16 MAR 2006
- Article first published online: 16 MAR 2006
- Received 3 November 2005; accepted 8 November 2005.
- gene expression;
- histone deacetylase 5;
- myocyte enhancer factor 2
- 1Skeletal muscle is a highly plastic tissue that has a remarkable ability to adapt to external demands, such as exercise. Many of these adaptations can be explained by changes in skeletal muscle gene expression. A single bout of exercise is sufficient to induce the expression of some metabolic genes. We have focused our attention on the regulation of glucose transporter isoform 4 (GLUT-4) expression in human skeletal muscle.
- 2Glucose transporter isoform 4 gene expression is increased immediately following a single bout of exercise, and the GLUT-4 enhancer factor (GEF) and myocyte enhancer factor 2 (MEF2) transcription factors are required for this response. Glucose transporter isoform enhancer factor and MEF2 DNA binding activities are increased following exercise, and the molecular mechanisms regulating MEF2 in exercising human skeletal muscle have also been examined.
- 3These studies find possible roles for histone deacetylase 5 (HDAC5), adenosine monophosphate–activated protein kinase (AMPK), peroxisome proliferator-activated receptor gamma coactivator 1α (PGC-1α) and p38 mitogen-activated protein kinase (MAPK) in regulating MEF2 through a series of complex interactions potentially involving MEF2 repression, coactivation and phosphorylation.
- 4Given that MEF2 is a transcription factor required for many exercise responsive genes, it is possible that these mechanisms are responsible for regulating the expression of a variety of metabolic genes during exercise. These mechanisms could also provide targets for the treatment and management of metabolic disease states, such as obesity and type 2 diabetes, which are characterized by mitochondrial dysfunction and insulin resistance in skeletal muscle.