4.7 Article

Proteomic Signatures of Human Visceral and Subcutaneous Adipocytes

期刊

出版社

ENDOCRINE SOC
DOI: 10.1210/clinem/dgab756

关键词

adipose tissue; visceral adipose tissue; subcutaneous adipose tissue; obesity; adipocytes; metabolism

资金

  1. CETOCOEN PLUS project [CZ.02.1.01/0.0/0.0/15_003/0000469 (CEP: EF15_003/0000469)]
  2. RECETOX research infrastructure (Ministry of Education, Youth and Sports of the Czech Republic) [LM2018121]
  3. CETOCOEN EXCELLENCE Teaming 2 project by Horizon2020 [857560]
  4. Ministry of Education, Youth and Sports of the Czech Republic [02.1.01/0.0/0.0/18_046/0015975, MUNI/A/1307/2019, MUNI/A/1246/2020]
  5. MEYS CR infrastructure project [LM2018127]
  6. e-Infrastruktura CZ project within the program Projects of Large Research, Development and Innovations Infrastructures [e-INFRA LM2018140]
  7. [MUNI/A/1615/2020]

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The study compared the proteomic profiles of mature adipocytes from different adipose tissue depots, with findings showing that subcutaneous adipocytes are more active in vesicular transport, secretion, and lipid metabolism, while visceral adipocytes have higher protein expression related to mitochondrial energy metabolism and translational or biosynthetic activity.
Context: Adipose tissue distribution is a key factor influencing metabolic health and risk in obesity-associated comorbidities. Objective: Here we aim to compare the proteomic profiles of mature adipocytes from different depots. Methods: Abdominal subcutaneous (SA) and omental visceral adipocytes (VA) were isolated from paired adipose tissue biopsies obtained during bariatric surgery on 19 severely obese women (body mass index > 30 kg/m(2)) and analyzed using state-of-the-art mass spectrometry. Differential expression analysis and weighted gene co-expression network analysis (WGCNA) were performed to investigate proteome signature properties and to examine a possible association of the protein expression with the clinical data. Results: We identified 3686 protein groups and found 1140 differentially expressed proteins (adj. P value < 0.05), of which 576 proteins were upregulated in SA and 564 in VA samples. We provide a global protein profile of abdominal SA and omental VA, present the most differentially expressed pathways and processes distinguishing SA from VA, and correlate them with clinical and body composition data. We show that SA are significantly more active in processes linked to vesicular transport and secretion, and to increased lipid metabolism activity. Conversely, the expression of proteins involved in the mitochondria! energy metabolism and translational or biosynthetic activity is higher in VA. Conclusion: Our analysis represents a valuable resource of protein expression profiles in abdominal SA and omental VA, highlighting key differences in their role in obesity.

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