Abstract

IntroductionSkeletal muscle mass and function decline with aging, and more precipitously after the age 75 y. To help provide insights into biologically relevant mechanisms for preserving muscle mass and function in advanced age, in this study we performed proteomics on skeletal muscle of world class octogenarian track and field athletes in comparison to healthy octogenarian non‐athletes.MethodsMuscle cross‐sectional area by MRI and a vastus lateralis muscle biopsy were performed in 15 octogenarian world class track and field athletes (8 of whom were world record holders in their discipline at the time of testing) and 14 non‐athlete age‐ and sex‐matched non‐athlete controls. From these subjects, a portion of muscle from a subset of 12 master athletes (MA mean age 81.19 ± 5.1 y) and 12 non‐athlete controls (NA mean age 80.94 ± 4.5 y) was used for liquid‐chromatography mass spectrometry to generate quantitative tandem mass tag proteomics data. In addition, we measured mtDNA copy number, COX/SDH histochemistry to identify respiratory compromised fibers, and Western blot of mitochondrial inner and outer membrane proteins.ResultsMuscle cross‐sectional area was higher in MA. Tandem mass spectrometry identified over 6000 proteins, and significant differences in abundance were found between NA controls and MA for more than 800 proteins. A pathway analysis revealed that pathways involved in mitochondria (e.g., TCA cycle, respiratory electron transport, cristae formation, sirtuins) were higher in MA, while proteins in pathways involved in the spliceosome and nuclear pore were downregulated in MA. Finally, 8 mtDNA‐encoded proteins that were included in the analysis were elevated in MA versus NA. These proteomics data are consistent with phenotypic data showing MA have higher mtDNA copy number, fewer respiratory chain compromised muscle fibers, and an increased ratio of ETC subunits (inner mitochondrial membrane proteins) relative to VDAC (outer mitochondrial membrane protein), suggesting an increase in cristae formation.ConclusionOur data underscore that mitochondrial pathways are key to maintaining a high level of physical function in advanced age. With the current study design we cannot determine the degree to which these differences are attributable to the physical activity habits of MA, but it is likely to play a role.Support or Funding InformationCIHR (MOP 125986 to RTH)NIA Intramural Research program

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