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Regulation of skeletal muscle mitochondrial function: genes to proteins Lanza IR; Sreekumaran Nair KActa Physiol (Oxf) 2010[Aug]; 199 (4): 529-47The impact of ageing on mitochondrial function and the deterministic role of mitochondria on senescence continue to be topics of vigorous debate. Many studies report that skeletal muscle mitochondrial content and function are reduced with ageing and metabolic diseases associated with insulin resistance. However, an accumulating body of literature suggests that physical inactivity typical of ageing may be a more important determinant of mitochondrial function than chronological age, per se. Reports of age-related declines in mitochondrial function have spawned a vast body of literature devoted to understanding the underlying mechanisms. These mechanisms include decreased abundance of mtDNA, reduced mRNA levels, as well as decreased synthesis and expression of mitochondrial proteins, ultimately resulting in decreased function of the whole organelle. Effective therapies to prevent, reverse or delay the onset of the aforementioned mitochondrial changes, regardless of their inevitability or precise underlying causes, require an intimate understanding of the processes that regulate mitochondrial biogenesis, which necessitates the coordinated regulation of nuclear and mitochondrial genomes. Herein we review the current thinking on regulation of mitochondrial biogenesis by transcription factors and transcriptional co-activators and the role of hormones and exercise in initiating this process. We review how exercise may help preserve mitochondrial content and functionality across the lifespan, and how physical inactivity is emerging as a major determinant of many age-associated changes at the level of the mitochondrion. We also review evidence that some mitochondrial changes with ageing are independent of exercise or physical activity and appear to be inevitable consequences of old age.|*Muscle, Skeletal/cytology/metabolism[MESH]|Adenosine Triphosphate/metabolism[MESH]|Aging/physiology[MESH]|Animals[MESH]|Cellular Senescence/physiology[MESH]|DNA, Mitochondrial/metabolism[MESH]|Exercise/*physiology[MESH]|Heat-Shock Proteins/metabolism[MESH]|Hormones/metabolism[MESH]|Humans[MESH]|Mitochondria, Muscle/*physiology[MESH]|Mitochondrial Proteins/metabolism[MESH]|Muscle Proteins/metabolism[MESH]|Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha[MESH]|Physical Endurance/physiology[MESH]|Signal Transduction/physiology[MESH]|Transcription Factors/metabolism[MESH] |
