Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice

被引:0
作者
Matthew D. Campbell
Miguel Martín-Pérez
Jarrett D. Egertson
Matthew J. Gaffrey
Lu Wang
Theo Bammler
Peter S. Rabinovitch
Michael MacCoss
Wei-Jun Qian
Judit Villen
David Marcinek
机构
[1] University of Washington,Department of Radiology
[2] South Lake Union Campus,Department of Genome Sciences
[3] University of Washington,Biological Sciences Division
[4] Pacific Northwest National Laboratory,Department of Environmental and Occupational Health Sciences
[5] University of Washington,Department of Laboratory Medicine and Pathology
[6] University of Washington,undefined
来源
GeroScience | 2022年 / 44卷
关键词
Aging; Mitochondria; Sarcopenia; Phosphorylation; Proteomics; S-Glutathionylation;
D O I
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中图分类号
学科分类号
摘要
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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页码:2913 / 2924
页数:11
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