Modifications in the myogenic program induced by in vivo and in vitro aging

• Published in: Gene 2005-02, Vol.347 (1), p.65-72
• Main Authors: Bortoli, Sylvie, Renault, Valérie, Mariage-Samson, Régine, Eveno, Eric, Auffray, Charles, Butler-Browne, Gill, Piétu, Geneviève
• Format: Article
• Language: English
• Subjects: Aged; Aging - genetics; Aging - physiology; Carbohydrate Metabolism; Cell Differentiation - genetics; Cell Differentiation - physiology; Cell Proliferation; Cells, Cultured; Cellular Senescence - genetics; Cellular Senescence - physiology; Child, Preschool; Citric Acid Cycle - genetics; Citric Acid Cycle - physiology; Electron Transport - genetics; Electron Transport - physiology; Female; Gene Expression Profiling; Gene Expression Regulation - genetics; Gene Expression Regulation - physiology; Glycolysis - genetics; Glycolysis - physiology; Humans; Life Sciences; Macroarrays; Male; Middle Aged; Mitochondria, Muscle - genetics; Mitochondria, Muscle - metabolism; Mitochondrial Proton-Translocating ATPases - genetics; Mitochondrial Proton-Translocating ATPases - metabolism; Muscle Development - genetics; Muscle Development - physiology; Muscle Fibers, Skeletal - metabolism; Muscle, Skeletal - physiology; Oligonucleotide Array Sequence Analysis; Satellite Cells, Skeletal Muscle - physiology; Skeletal muscle; Transcriptome
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/j.gene.2004.12.029

In this study, we have used high density cDNA arrays to assess age-related changes in gene expression in the myogenic program of human satellite cells and to elucidate modifications in differentiation capacity that could occur throughout in vitro cellular aging. We have screened a collection of 2016 clones from a human skeletal muscle 3′-end cDNA library in order to investigate variations in the myogenic program of myotubes formed by the differentiation of myoblasts of individuals with different ages (5 days old, 52 years old and 79 years old) and induced to differentiate at different stages of their lifespan (early proliferation, presenescence and senescence). Although our analysis has not been able to underline specific changes in the expression of genes encoding proteins involved in muscle structure and/or function, we have demonstrated an age-related induction of genes involved in stress response and a down-regulation of genes involved both in mitochondrial electron transport/ATP synthase and in glycolysis/TCA cycle. From this global approach of post-mitotic cell aging, we have identified 2 potential new markers of presenescence for human myotubes, both strongly linked to carbohydrate metabolism, which could be useful in developing therapeutic strategies.