Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice

GeroScience - Tập 44 - Trang 2913-2924 - 2022
Matthew D. Campbell1, Miguel Martín-Pérez2, Jarrett D. Egertson2, Matthew J. Gaffrey3, Lu Wang4, Theo Bammler, Peter S. Rabinovitch5, Michael MacCoss2, Wei-Jun Qian3, Judit Villen2, David Marcinek1,5
1Department of Radiology, University of Washington, South Lake Union Campus, Seattle, USA
2Department of Genome Sciences, University of Washington, Seattle, USA
3Biological Sciences Division, Pacific Northwest National Laboratory, Richland, USA
4Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, USA
5Department of Laboratory Medicine and Pathology, University of Washington, Seattle, USA

Tóm tắt

The age-related decline in skeletal muscle mass and function is known as sarcopenia. Sarcopenia progresses based on complex processes involving protein dynamics, cell signaling, oxidative stress, and repair. We have previously found that 8-week treatment with elamipretide improves skeletal muscle function, reverses redox stress, and restores protein S-glutathionylation changes in aged female mice. This study tested whether 8-week treatment with elamipretide also affects global phosphorylation in skeletal muscle consistent with functional improvements and S-glutathionylation. Using female 6–7-month-old mice and 28–29-month-old mice, we found that phosphorylation changes did not relate to S-glutathionylation modifications, but that treatment with elamipretide did partially reverse age-related changes in protein phosphorylation in mouse skeletal muscle.

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