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Involvement of guanylin and GC-C in rat mesenteric macrophages in resistance to a high-fat diet

机译:鸟苷和GC-C参与大鼠肠系膜巨噬细胞对高脂饮食的抵抗

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摘要

A high-fat diet (HFD) is a well-known contributing factor in the development of obesity. Most rats fed HFDs become obese. Those that avoid obesity when fed HFDs are considered diet resistant (DR). We performed a microarray screen to identify genes specific to the mesenteric fat of DR rats and revealed high expression of guanylin and guanylyl cyclase C (GC-C) in some subjects. Our histologic studies revealed that the cellular source of guanylin and GC-C is macrophages. Therefore, we developed double-transgenic (Tg) rats overexpressing guanylin and GC-C in macrophages and found that they were resistant to the effects of HFDs. In the mesenteric fat of HFD-fed Tg rats, Fas and perilipin mRNAs were downregulated, and those of genes involved in fatty acid oxidation were upregulated, compared with the levels in HFD-fed wild-type rats. In vitro studies demonstrated that lipid accumulation was markedly inhibited in adipocytes cocultured with macrophages expressing guanylin and GC-C and that this inhibition was reduced after treatment with guanylin- and GC-C-specific siRNAs. Our results suggest that the macrophagic guanylin-GC-C system contributes to the altered expression of genes involved in lipid metabolism, leading to resistance to obesity.
机译:高脂饮食(HFD)是肥胖症发展的众所周知的因素。饲喂HFD的大多数大鼠变得肥胖。那些在喂食HFD时避免肥胖的人被认为是抗饮食(DR)的。我们进行了微阵列筛选,以鉴定DR大鼠肠系膜脂肪特异的基因,并揭示了某些受试者中鸟苷和鸟苷酸环化酶C(GC-C)的高表达。我们的组织学研究表明鸟苷和GC-C的细胞来源是巨噬细胞。因此,我们开发了在巨噬细胞中过表达鸟苷和GC-C的双转基因(Tg)大鼠,发现它们对HFD的作用具有抗性。与HFD喂养的野生型大鼠相比,在HFD喂养的Tg大鼠的肠系膜脂肪中,Fas和外周血脂mRNA的表达被下调,而与脂肪酸氧化有关的基因的Fas和perilipin mRNA的表达被上调。体外研究表明,与表达鸟苷蛋白和GC-C的巨噬细胞共培养的脂肪细胞中脂质蓄积受到显着抑制,并且在用鸟苷蛋白和GC-C特异性siRNA处理后,这种抑制作用得以降低。我们的结果表明,巨噬细胞鸟苷-GC-C系统有助于脂质代谢相关基因的表达改变,从而导致对肥胖的抵抗力。

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