High-throughput proteomics uncovers exercise training and type 2 diabetes-induced changes in human white adipose tissue.
Jeppe Kjærgaard LarsenRikke KruseNavid SahebekhtiariRoger Moreno-JusticiaGerard Gomez JorbaMaria H PetersenMartin Eisemann de AlmeidaNiels ØrtenbladAtul Shahaji DeshmukhKurt HøjlundPublished in: Science advances (2023)
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.
Keyphrases
- adipose tissue
- type diabetes
- insulin resistance
- high throughput
- mass spectrometry
- metabolic syndrome
- weight loss
- endothelial cells
- high fat diet
- high intensity
- skeletal muscle
- liquid chromatography
- induced pluripotent stem cells
- high fat diet induced
- bariatric surgery
- weight gain
- glycemic control
- blood pressure
- single cell
- bone mineral density
- body mass index
- ms ms
- dna methylation
- pluripotent stem cells
- climate change
- gestational age
- capillary electrophoresis
- diabetic rats