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肥胖症中脂肪组织和血清 CCDC80 及其与相关代谢性疾病的关系。

Adipose tissue and serum CCDC80 in obesity and its association with related metabolic disease.

机构信息

CIBER de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM)-Instituto de Salud Carlos III, Spain.

Departament de Bioquímica i Biologia Molecular, Institut de Biomedicina de la Universitat de Barcelona, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.

出版信息

Mol Med. 2017 Oct;23:225-234. doi: 10.2119/molmed.2017.00067. Epub 2017 Aug 23.

Abstract

Coiled-coil domain-containing 80 (CCDC80) is an adipocyte-secreted protein that modulates glucose homeostasis in response to diet-induced obesity in mice. The objective of this study is to analyze the link between human CCDC80 and obesity. CCDC80 protein expression was assessed in paired visceral (VAT) and subcutaneous (SAT) adipose tissue from 10 subjects (BMI range 22.4-38.8 kg/m). Circulating CCDC80 levels were quantified in serum samples from two independent cross-sectional cohorts comprising 33 lean and 15 obese (cohort 1) and 32 morbid obese (cohort 2) male subjects. Insulin sensitivity, insulin secretion and blood neutrophil count were quantified in serum samples from both cohorts. Additionally, circulating free IGF-1 levels and oral glucose tolerance tests (OGTT) were assessed in cohort 1 whereas C-reactive protein levels and degree of atherosclerosis and hepatic steatosis were studied in cohort 2. In lean subjects, total CCDC80 protein content assessed by immunoblotting was lower in VAT than in SAT. In obese patients, CCDC80 was increased in VAT (<0.05), but equivalent in SAT compared with lean counterparts. In cohort 1, serum CCDC80 correlated negatively with the acute insulin response to glucose and IGF1 levels, and positively with blood neutrophil count, independently of BMI, but not with insulin sensitivity. In cohort 2, serum CCDC80 was positively linked to the inflammatory biomarker C-reactive protein (r=0.46; =0.009), atherosclerosis (carotid intima-media thickness, r=0.62; <0.001) and hepatic steatosis (ANOVA =0.025). Overall, these results suggest for the first time that CCDC80 may be a component of the obesity-altered secretome in VAT and could act as an adipokine whose circulant levels are linked to glucose tolerance derangements and related to inflammation-associated chronic complications.

摘要

卷曲螺旋结构域蛋白 80(CCDC80)是一种脂肪细胞分泌的蛋白,可调节小鼠饮食诱导肥胖时的葡萄糖稳态。本研究旨在分析人类 CCDC80 与肥胖之间的关系。评估了 10 名受试者(BMI 范围为 22.4-38.8kg/m²)配对的内脏(VAT)和皮下(SAT)脂肪组织中的 CCDC80 蛋白表达。在两个独立的横断面队列的血清样本中定量了循环 CCDC80 水平,这些队列包括 33 名瘦人和 15 名肥胖者(队列 1)和 32 名病态肥胖者(队列 2)男性受试者。在两个队列的血清样本中定量了胰岛素敏感性、胰岛素分泌和血液中性粒细胞计数。此外,在队列 1 中评估了循环游离 IGF-1 水平和口服葡萄糖耐量试验(OGTT),而在队列 2 中研究了 C-反应蛋白水平以及动脉粥样硬化和肝脂肪变性的程度。在瘦受试者中,通过免疫印迹法评估的总 CCDC80 蛋白含量在 VAT 中低于 SAT。在肥胖患者中,VAT 中的 CCDC80 增加(<0.05),但与瘦受试者相比,SAT 中的 CCDC80 相当。在队列 1 中,血清 CCDC80 与葡萄糖的急性胰岛素反应和 IGF1 水平呈负相关,与血液中性粒细胞计数呈正相关,与 BMI 无关,但与胰岛素敏感性无关。在队列 2 中,血清 CCDC80 与炎症生物标志物 C-反应蛋白(r=0.46;=0.009)、动脉粥样硬化(颈动脉内膜-中层厚度,r=0.62;<0.001)和肝脂肪变性(ANOVA =0.025)呈正相关。总的来说,这些结果首次表明 CCDC80 可能是 VAT 中肥胖改变的分泌组的一个组成部分,并且可以作为一种脂肪因子发挥作用,其循环水平与葡萄糖耐量紊乱有关,并与炎症相关的慢性并发症有关。

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