期刊
ELIFE
卷 11, 期 -, 页码 -出版社
eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.80014
关键词
proteomics; signaling; muscle; Mouse
类别
资金
- National Institute of Diabetes and Digestive and Kidney Diseases [DK125260, DK111916, DK116074]
- American Heart Association [905674, 18POST34030448, 882082]
- National Heart, Lung, and Blood Institute [T32HL007057]
- National Institute on Aging [R21AG065943]
- NIH Office of the Director [K01AG05666]
The secreted protein Ism1 mitigates diabetes by increasing glucose uptake in adipocytes and skeletal muscles through the activation of the PI3K-Akt pathway. Phosphoproteomic analysis reveals overlapping and distinct signaling pathways of Ism1 and insulin. Ism1 affects protein translation, the mTOR pathway, and muscle function through unknown phosphorylation sites, and its ablation leads to altered proteostasis and reduced muscle protein content.
The secreted protein isthmin-1 (Ism1) mitigates diabetes by increasing adipocyte and skeletal muscle glucose uptake by activating the PI3K-Akt pathway. However, while both Ism1 and insulin converge on these common targets, Ism1 has distinct cellular actions suggesting divergence in downstream intracellular signaling pathways. To understand the biological complexity of Ism1 signaling, we performed phosphoproteomic analysis after acute exposure, revealing overlapping and distinct pathways of Ism1 and insulin. We identify a 53% overlap between Ism1 and insulin signaling and Ism1-mediated phosphoproteome-wide alterations in similar to 450 proteins that are not shared with insulin. Interestingly, we find several unknown phosphorylation sites on proteins related to protein translation, mTOR pathway, and, unexpectedly, muscle function in the Ism1 signaling network. Physiologically, Ism1 ablation in mice results in altered proteostasis, including lower muscle protein levels under fed and fasted conditions, reduced amino acid incorporation into proteins, and reduced phosphorylation of the key protein synthesis effectors Akt and downstream mTORC1 targets. As metabolic disorders such as diabetes are associated with accelerated loss of skeletal muscle protein content, these studies define a non-canonical mechanism by which this antidiabetic circulating protein controls muscle biology.
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