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Obesity-associated exosomal miRNAs modulate glucose and lipid metabolism in mice

机译:肥胖相关的外泌体miRNA调节小鼠的葡萄糖和脂质代谢

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摘要

Obesity is frequently associated with metabolic disease. Here, we show that obesity changes the miRNA profile of plasma exosomes in mice, including increases in miR-122, miR-192, miR-27a-3p, and miR-27b-3p. Importantly, treatment of lean mice with exosomes isolated from obese mice induces glucose intolerance and insulin resistance. Moreover, administration of control exosomes transfected with obesity-associated miRNA mimics strongly induces glucose intolerance in lean mice and results in central obesity and hepatic steatosis. Expression of the candidate target gene Ppara is decreased in white adipose tissue but not in the liver of mimic-treated (MIMIC) mice, and this is accompanied by increased circulating free fatty acids and hypertriglyceridemia. Treatment with a specific siRNA targeting Ppara transfected into exosomes recapitulates the phenotype induced by obesity-associated miRNAs. Importantly, simultaneously reducing free fatty acid plasma levels in MIMIC mice with either the lipolysis inhibitor acipimox or the PPARα agonist fenofibrate partially protects against these metabolic alterations. Overall, our data highlight the central role of obesity-associated exosomal miRNAs in the etiopathogeny of glucose intolerance and dyslipidemia.
机译:肥胖经常与代谢疾病有关。在这里,我们显示肥胖会改变小鼠血浆外泌体的miRNA谱,包括增加miR-122,miR-192,miR-27a-3p和miR-27b-3p。重要的是,用从肥胖小鼠中分离的外来体处理瘦小鼠会引起葡萄糖耐量和胰岛素抵抗。而且,施用与肥胖相关的miRNA模拟物转染的对照外泌体强烈诱导了瘦小鼠的葡萄糖耐受不良,并导致中枢性肥胖和肝脂肪变性。候选目标基因Ppara的表达在白色脂肪组织中降低,但在模拟治疗(MIMIC)小鼠的肝脏中却没有降低,这伴随着循环脂肪酸和高甘油三酯血症的增加。用转染到外泌体中的靶向Ppara的特异性siRNA进行治疗,可以概括肥胖相关miRNA诱导的表型。重要的是,同时使用脂解抑制剂阿西莫司或PPARα激动剂非诺贝特降低MIMIC小鼠中的游离脂肪酸血浆水平可部分防止这些代谢改变。总体而言,我们的数据突出了与肥胖相关的外泌体miRNA在葡萄糖耐受不良和血脂异常的病因中的核心作用。

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