Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
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
Descripción
Sumario: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.