Personalized phosphoproteomics of skeletal muscle insulin resistance and exercise links MINDY1 to insulin action

Type 2 diabetes is preceded by a defective insulin response, yet our knowledge of the precise mechanisms is incomplete. Here, we investigate how insulin resistance alters skeletal muscle signaling and how exercise partially counteracts this effect. We measured parallel phenotypes and phosphoproteomes of insulin-resistant (IR) and insulin-sensitive (IS) men as they responded to exercise and insulin (n = 19, 114 biopsies), quantifying over 12,000 phosphopeptides in each biopsy. Insulin resistance involves selective and time-dependent alterations to signaling, including reduced insulin-stimulated mTORC1 and non-canonical signaling responses. Prior exercise promotes insulin sensitivity even in IR individuals by "priming" a portion of insulin signaling prior to insulin infusion. This includes MINDY1 S441, which we show is an AKT substrate. We found that MINDY1 knockdown enhances insulin-stimulated glucose uptake in rat myotubes. This work delineates the signaling alterations in IR skeletal muscle and identifies MINDY1 as a regulator of insulin action.

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Publication Details

Journal
Cell Metabolism
Published
2024-11-21
DOI
https://doi.org/10.1016/j.cmet.2024.10.020
Citations
18
Primary Topic
Advanced Proteomics Techniques and Applications
Type
article
Field-Weighted Citation Impact
4.33

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article

Personalized phosphoproteomics of skeletal muscle insulin resistance and exercise links MINDY1 to insulin action

Janne R. Hingst, Alexis Díaz‐Vegas, Elise J. Needham, Erik A. Richter et al.
18 citations
Cell Metabolism
Advanced Proteomics Techniques and Applications
4.33
article

Personalized phosphoproteomics of skeletal muscle insulin resistance and exercise links MINDY1 to insulin action

Janne R. Hingst, Alexis Díaz‐Vegas, Elise J. Needham, Erik A. Richter, David Ernest James, Benjamin L. Parker, Kurt Højlund, Jørgen F. P. Wojtaszewski, Sean J. Humphrey, Kristen C. Cooke, Kohei Kido, Jonas M. Kristensen, Magnus R. Leandersson, Hannah Huckstep, Johan Onslev, Christian Pehmøller, Guang Yang
article en
18 citations

Abstract

Type 2 diabetes is preceded by a defective insulin response, yet our knowledge of the precise mechanisms is incomplete. Here, we investigate how insulin resistance alters skeletal muscle signaling and how exercise partially counteracts this effect. We measured parallel phenotypes and phosphoproteomes of insulin-resistant (IR) and insulin-sensitive (IS) men as they responded to exercise and insulin (n = 19, 114 biopsies), quantifying over 12,000 phosphopeptides in each biopsy. Insulin resistance involves selective and time-dependent alterations to signaling, including reduced insulin-stimulated mTORC1 and non-canonical signaling responses. Prior exercise promotes insulin sensitivity even in IR individuals by "priming" a portion of insulin signaling prior to insulin infusion. This includes MINDY1 S441, which we show is an AKT substrate. We found that MINDY1 knockdown enhances insulin-stimulated glucose uptake in rat myotubes. This work delineates the signaling alterations in IR skeletal muscle and identifies MINDY1 as a regulator of insulin action.

Cell MetabolismVol. 36(12)
University of Copenhagen (DK), The University of Sydney (AU), Royal Children's Hospital (AU), Pfizer (United States) (US), Murdoch Children's Research Institute (AU)
Pfizer, Australian Government, British Heart Foundation, European Foundation for the Study of Diabetes, University of Sydney, Novo Nordisk, Novo Nordisk Fonden, Medical Research Council, National Health and Medical Research Council, Japan Society for the Promotion of Science
Zero hunger
Openalex Percentile: Top 4%
Advanced Proteomics Techniques and Applications
4.33
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