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High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue
White adipose tissue (WAT) is important for metabolic homeostasis. We established the differential proteomic signatures of WAT in glucose-tolerant lean and obese individuals and patients with type 2 diabetes (T2D) and the response to 8 weeks of high-intensity interval training (HIIT). Using a high-t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686561/ https://www.ncbi.nlm.nih.gov/pubmed/38019916 http://dx.doi.org/10.1126/sciadv.adi7548 |
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author | Larsen, Jeppe Kjærgaard Kruse, Rikke Sahebekhtiari, Navid Moreno-Justicia, Roger Gomez Jorba, Gerard Petersen, Maria H. de Almeida, Martin E. Ørtenblad, Niels Deshmukh, Atul S. Højlund, Kurt |
author_facet | Larsen, Jeppe Kjærgaard Kruse, Rikke Sahebekhtiari, Navid Moreno-Justicia, Roger Gomez Jorba, Gerard Petersen, Maria H. de Almeida, Martin E. Ørtenblad, Niels Deshmukh, Atul S. Højlund, Kurt |
author_sort | Larsen, Jeppe Kjærgaard |
collection | PubMed |
description | White adipose tissue (WAT) is important for metabolic homeostasis. We established the differential proteomic signatures of WAT in glucose-tolerant lean and obese individuals and patients with type 2 diabetes (T2D) and the response to 8 weeks of high-intensity interval training (HIIT). Using a high-throughput and reproducible mass spectrometry–based proteomics pipeline, we identified 3773 proteins and found that most regulated proteins displayed progression in markers of dysfunctional WAT from lean to obese to T2D individuals and were highly associated with clinical measures such as insulin sensitivity and HbA1c. We propose that these distinct markers could serve as potential clinical biomarkers. HIIT induced only minor changes in the WAT proteome. This included an increase in WAT ferritin levels independent of obesity and T2D, and WAT ferritin levels were strongly correlated with individual insulin sensitivity. Together, we report a proteomic signature of WAT related to obesity and T2D and highlight an unrecognized role of human WAT iron metabolism in exercise training adaptations. |
format | Online Article Text |
id | pubmed-10686561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106865612023-11-30 High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue Larsen, Jeppe Kjærgaard Kruse, Rikke Sahebekhtiari, Navid Moreno-Justicia, Roger Gomez Jorba, Gerard Petersen, Maria H. de Almeida, Martin E. Ørtenblad, Niels Deshmukh, Atul S. Højlund, Kurt Sci Adv Biomedicine and Life Sciences White adipose tissue (WAT) is important for metabolic homeostasis. We established the differential proteomic signatures of WAT in glucose-tolerant lean and obese individuals and patients with type 2 diabetes (T2D) and the response to 8 weeks of high-intensity interval training (HIIT). Using a high-throughput and reproducible mass spectrometry–based proteomics pipeline, we identified 3773 proteins and found that most regulated proteins displayed progression in markers of dysfunctional WAT from lean to obese to T2D individuals and were highly associated with clinical measures such as insulin sensitivity and HbA1c. We propose that these distinct markers could serve as potential clinical biomarkers. HIIT induced only minor changes in the WAT proteome. This included an increase in WAT ferritin levels independent of obesity and T2D, and WAT ferritin levels were strongly correlated with individual insulin sensitivity. Together, we report a proteomic signature of WAT related to obesity and T2D and highlight an unrecognized role of human WAT iron metabolism in exercise training adaptations. American Association for the Advancement of Science 2023-11-29 /pmc/articles/PMC10686561/ /pubmed/38019916 http://dx.doi.org/10.1126/sciadv.adi7548 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Larsen, Jeppe Kjærgaard Kruse, Rikke Sahebekhtiari, Navid Moreno-Justicia, Roger Gomez Jorba, Gerard Petersen, Maria H. de Almeida, Martin E. Ørtenblad, Niels Deshmukh, Atul S. Højlund, Kurt High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue |
title | High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue |
title_full | High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue |
title_fullStr | High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue |
title_full_unstemmed | High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue |
title_short | High-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue |
title_sort | high-throughput proteomics uncovers exercise training and type 2 diabetes–induced changes in human white adipose tissue |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686561/ https://www.ncbi.nlm.nih.gov/pubmed/38019916 http://dx.doi.org/10.1126/sciadv.adi7548 |
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