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CILAIR-Based Secretome Analysis of Obese Visceral and Subcutaneous Adipose Tissues Reveals Distinctive ECM Remodeling and Inflammation Mediators

机译:基于CILAIR的肥胖内脏和皮下脂肪组织的分泌素分析显示了独特的ECM重塑和炎症介体

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摘要

In the context of obesity, strong evidences support a distinctive pathological contribution of adipose tissue depending on its anatomical site of accumulation. Therefore, subcutaneous adipose tissue (SAT) has been lately considered metabolically benign compared to visceral fat (VAT), whose location is associated to the risk of developing cardiovascular disease, insulin resistance, and other associated comorbidities. Under the above situation, the chronic local inflammation that characterizes obese adipose tissue, has acquired a major role on the pathogenesis of obesity. In this work, we have analyzed for the first time human obese VAT and SAT secretomes using an improved quantitative proteomic approach for the study of tissue secretomes, Comparison of Isotope-Labeled Amino acid Incorporation Rates (CILAIR). The use of double isotope-labeling-CILAIR approach to analyze VAT and SAT secretomes allowed the identification of location-specific secreted proteins and its differential secretion. Additionally to the very high percentage of identified proteins previously implicated in obesity or in its comorbidities, this approach was revealed as a useful tool for the study of the obese adipose tissue microenvironment including extracellular matrix (ECM) remodeling and inflammatory status. The results herein presented reinforce the fact that VAT and SAT depots have distinct features and contribute differentially to metabolic disease.
机译:在肥胖的背景下,有力的证据支持脂肪组织在解剖学上的积累,这是脂肪组织独特的病理学贡献。因此,与内脏脂肪(VAT)相比,近来皮下脂肪组织(SAT)在代谢方面被认为是良性的,内脏脂肪(VAT)的位置与发生心血管疾病,胰岛素抵抗和其他相关合并症的风险有关。在上述情况下,以肥胖的脂肪组织为特征的慢性局部炎症已在肥胖的发病机理中发挥了重要作用。在这项工作中,我们首次使用改良的定量蛋白质组学方法研究人肥胖的VAT和SAT分泌组,以研究组织分泌组,即同位素标记的氨基酸掺入率的比较(CILAIR)。使用双重同位素标记-CILAIR方法分析VAT和SAT分泌组可以鉴定出位置特异性分泌蛋白及其差异分泌。除了以前与肥胖症或合并症有关的鉴定蛋白质的比例很高以外,这种方法还被认为是研究肥胖脂肪组织微环境(包括细胞外基质(ECM)重塑和炎症状态)的有用工具。本文提供的结果加强了以下事实:增值税和SAT库具有独特的特征,并在代谢疾病中有不同的贡献。

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