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Perilipin-2 deletion promotes carbohydrate-mediated browning of white adipose tissue at ambient temperature

机译:Perilipin-2缺失促进环境温度下碳水化合物介导的白色脂肪组织褐变

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摘要

Mice lacking perilipin-2 (Plin2-null) are resistant to obesity, insulin resistance, and fatty liver induced by Western or high-fat diets. In the current study, we found that, compared with WT mice on Western diet, Plin2-null adipose tissue was more insulin sensitive and inguinal subcutaneous white adipose tissue (iWAT) exhibited profound browning and robust induction of thermogenic and carbohydrate-responsive genetic programs at room temperature. Surprisingly, these Plin2-null responses correlated with the content of simple carbohydrates, rather than fat, in the diet, and were independent of adipose Plin2 expression. To define Plin2 and sugar effects on adipose browning, WT and Plin2-null mice were placed on chow diets containing 20% sucrose in their drinking water for 6 weeks. Compared with WT mice, iWAT of Plin2-null mice exhibited pronounced browning and striking increases in the expression of thermogenic and insulin-responsive genes on this diet. Significantly, Plin2-null iWAT browning was associated with reduced sucrose intake and elevated serum fibroblast growth factor (FGF)21 levels, which correlated with greatly enhanced hepatic FGF21 production. These data identify Plin2 actions as novel mediators of sugar-induced adipose browning through indirect effects of hepatic FGF21 expression, and suggest that adipose browning mechanisms may contribute to Plin2-null resistance to obesity.
机译:缺乏periplin-2(Plin2-null)的小鼠对西方饮食或高脂饮食诱导的肥胖,胰岛素抵抗和脂肪肝具有抵抗力。在当前的研究中,我们发现,与西方饮食中的WT小鼠相比,Plin2无脂肪组织对胰岛素更敏感,腹股沟皮下白色脂肪组织(iWAT)表现出深褐色并强烈诱导产热和碳水化合物反应性遗传程序。室内温度。令人惊讶的是,这些Plin2无效反应与饮食中简单碳水化合物而不是脂肪的含量相关,并且与脂肪Plin2表达无关。为了确定Plin2和糖对脂肪褐变的影响,将WT和Plin2-null小鼠置于其饮食中含20%蔗糖的低脂饮食6周。与WT小鼠相比,Plin2-null小鼠的iWAT在这种饮食中表现出明显的褐变,并显着增加了致热和胰岛素反应基因的表达。值得注意的是,Plin2无效的iWAT褐变与蔗糖摄入减少和血清成纤维细胞生长因子(FGF)21水平升高有关,这与肝FGF21的产生大大增加有关。这些数据通过肝FGF21表达的间接作用将Plin2的作用鉴定为糖诱导的脂肪褐变的新介体,并表明脂肪褐变的机制可能有助于Plin2对肥胖的抵抗。

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