Relevance of omental pericellular adipose tissue collagen in the pathophysiology of human abdominal obesity and related cardiometabolic risk

被引:32
|
作者
Michaud, A. [1 ,2 ,3 ]
Tordjman, J. [4 ,5 ]
Pelletier, M. [1 ]
Liu, Y. [4 ,5 ]
Laforest, S. [1 ,2 ,3 ]
Noel, S. [6 ]
Le Naour, G. [7 ]
Bouchard, C. [6 ]
Clement, K. [4 ,5 ]
Tchernof, A. [1 ,2 ,3 ]
机构
[1] Univ Laval, CHU Quebec, Dept Endocrinol & Nephrol, 2705 Laurier Blvd,R 4779, Quebec City, PQ G1V 4G2, Canada
[2] Univ Laval, Sch Nutr, Quebec City, PQ, Canada
[3] Quebec Heart & Lung Inst, Quebec City, PQ, Canada
[4] Hop La Pitie Salpetriere, AP HP, Dept Nutr, Inst Cardiometab & Nutr, Paris, France
[5] UPMC Univ Paris 06, Sorbonne Univ, Paris, France
[6] Univ Laval, Med Ctr, Gynecol Unit, Ville De Quebec, PQ, Canada
[7] UPMC Univ Paris 06, Dept Pathol, Pitie Salpetriere Hosp, AP HP,UIMAP, Paris, France
基金
加拿大健康研究院;
关键词
EXTRACELLULAR-MATRIX; MACROPHAGE INFILTRATION; INSULIN-RESISTANCE; FIBROSIS; DIFFERENTIATION; VI; ACCUMULATION; ADIPOCYTES; EXPRESSION; COL6A3;
D O I
10.1038/ijo.2016.173
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Adipose tissue fibrosis is a relatively new notion and its relationship with visceral obesity and cardiometabolic alterations remains unclear, particularly in moderate obesity. OBJECTIVE: Our objective was to examine if total and pericellular collagen accumulation are relevant for the pathophysiology of visceral obesity and related cardiometabolic risk. SUBJECTS AND METHODS: Surgical omental (OM) and subcutaneous (SC) fat samples were obtained in 56 women (age: 47.2 +/- 5.8 years; body mass index (BMI): 27.1 +/- 4.4 kg/m(2)). Body composition and fat distribution were measured by dual-energy X-ray absorptiometry and computed tomography, respectively. Total and pericellular collagen were measured using picrosirius red staining. CD68+ cells (total macrophages) and CD163+ cells (M2-macrophages) were identified using immunohistochemistry. RESULTS: We found that only pericellular collagen percentage, especially in OM fat, was associated with higher BMI, body fat mass and adipose tissue areas as well as lower radiologic attenuation of visceral adipose tissue and altered cardiometabolic risk variables. Strong correlations between peri-adipocyte collagen percentage and total or M2-macrophage percentages were observed in both depots. Total collagen percentage in either compartment was not related to adiposity, fat distribution or cardiometabolic risk. CONCLUSIONS: As opposed to whole tissue-based assessments of adipose tissue fibrosis, collagen deposition around the adipocyte, especially in the OM fat compartment is related to total and regional adiposity as well as altered cardiometabolic risk profile.
引用
收藏
页码:1823 / 1831
页数:9
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