TY - JOUR
T1 - Physical activity associated proteomics of skeletal muscle
T2 - Being proteomics of skeletal muscle: Being physically active in daily life may protect skeletal muscle from aging
AU - Ubaida-Mohien, Ceereena
AU - Gonzalez-Freire, Marta
AU - Lyashkov, Alexey
AU - Moaddel, Ruin
AU - Chia, Chee W.
AU - Simonsick, Eleanor M.
AU - Sen, Ranjan
AU - Ferrucci, Luigi
N1 - Funding Information:
This work was supported by the Intramural Research Program of the National Institute on Aging, NIH, Baltimore, MD, United States.
Publisher Copyright:
© 2019 Ubaida-Mohien, Gonzalez-Freire, Lyashkov, Moaddel, Chia, Simonsick, Sen and Ferrucci.
PY - 2019
Y1 - 2019
N2 - Muscle strength declines with aging and increasing physical activity is the only intervention known to attenuate this decline. In order to adequately investigate both preventive and therapeutic interventions against sarcopenia, a better understanding of the biological changes that are induced by physical activity in skeletal muscle is required. To determine the effect of physical activity on the skeletal muscle proteome, we utilized liquid-chromatography mass spectrometry to obtain quantitative proteomics data on human skeletal muscle biopsies from 60 well-characterized healthy individuals (20-87 years) who reported heterogeneous levels of physical activity (not active, active, moderately active, and highly active). Over 4,000 proteins were quantified, and higher self-reported physical activity was associated with substantial overrepresentation of proteins associated with mitochondria, TCA cycle, structural and contractile muscle, and genome maintenance. Conversely, proteins related to the spliceosome, transcription regulation, immune function, and apoptosis, DNA damage, and senescence were underrepresented with higher self-reported activity. These differences in observed protein expression were related to different levels of physical activity in daily life and not intense competitive exercise. In most instances, differences in protein levels were directly opposite to those reported in the literature observed with aging. These data suggest that being physically active in daily life has strong and biologically detectable beneficial effects on muscle.
AB - Muscle strength declines with aging and increasing physical activity is the only intervention known to attenuate this decline. In order to adequately investigate both preventive and therapeutic interventions against sarcopenia, a better understanding of the biological changes that are induced by physical activity in skeletal muscle is required. To determine the effect of physical activity on the skeletal muscle proteome, we utilized liquid-chromatography mass spectrometry to obtain quantitative proteomics data on human skeletal muscle biopsies from 60 well-characterized healthy individuals (20-87 years) who reported heterogeneous levels of physical activity (not active, active, moderately active, and highly active). Over 4,000 proteins were quantified, and higher self-reported physical activity was associated with substantial overrepresentation of proteins associated with mitochondria, TCA cycle, structural and contractile muscle, and genome maintenance. Conversely, proteins related to the spliceosome, transcription regulation, immune function, and apoptosis, DNA damage, and senescence were underrepresented with higher self-reported activity. These differences in observed protein expression were related to different levels of physical activity in daily life and not intense competitive exercise. In most instances, differences in protein levels were directly opposite to those reported in the literature observed with aging. These data suggest that being physically active in daily life has strong and biologically detectable beneficial effects on muscle.
KW - DNA damage
KW - Immunity
KW - Mass spectrometry
KW - Mitochondria
KW - Physical activity
KW - Proteomics
KW - Skeletal muscle
KW - Spliceosome
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U2 - 10.3389/fphys.2019.00312
DO - 10.3389/fphys.2019.00312
M3 - Article
C2 - 30971946
AN - SCOPUS:85066626703
SN - 1664-042X
VL - 10
JO - Frontiers in Physiology
JF - Frontiers in Physiology
IS - MAR
M1 - 312
ER -