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Subtype-Specific Surface Proteins on Adipose Tissue Macrophages and Their Association to Obesity-Induced Insulin Resistance.

Authors :
Strand K
Stiglund N
Haugstøyl ME
Kamyab Z
Langhelle V
Lawrence-Archer L
Busch C
Cornillet M
Hjellestad ID
Nielsen HJ
Njølstad PR
Mellgren G
Björkström NK
Fernø J
Source :
Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2022 Apr 11; Vol. 13, pp. 856530. Date of Electronic Publication: 2022 Apr 11 (Print Publication: 2022).
Publication Year :
2022

Abstract

A chronic low-grade inflammation, originating in the adipose tissue, is considered a driver of obesity-associated insulin resistance. Macrophage composition in white adipose tissue is believed to contribute to the pathogenesis of metabolic diseases, but a detailed characterization of pro- and anti-inflammatory adipose tissue macrophages (ATMs) in human obesity and how they are distributed in visceral- and subcutaneous adipose depots is lacking. In this study, we performed a surface proteome screening of pro- and anti-inflammatory ATMs in both subcutaneous- (SAT) and visceral adipose tissue (VAT) and evaluated their relationship with systemic insulin resistance. From the proteomics screen we found novel surface proteins specific to M1-like- and M2-like macrophages, and we identified depot-specific immunophenotypes in SAT and VAT. Furthermore, we found that insulin resistance, assessed by HOMA-IR, was positively associated with a relative increase in pro-inflammatory M1-like macrophages in both SAT and VAT.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Strand, Stiglund, Haugstøyl, Kamyab, Langhelle, Dyer, Busch, Cornillet, Hjellestad, Nielsen, Njølstad, Mellgren, Björkström and Fernø.)

Details

Language :
English
ISSN :
1664-2392
Volume :
13
Database :
MEDLINE
Journal :
Frontiers in endocrinology
Publication Type :
Academic Journal
Accession number :
35480482
Full Text :
https://doi.org/10.3389/fendo.2022.856530