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首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >SPARC is over-expressed in adipose tissues of diet-induced obese rats and causes insulin resistance in 3T3-L1 adipocytes
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SPARC is over-expressed in adipose tissues of diet-induced obese rats and causes insulin resistance in 3T3-L1 adipocytes

机译:SPARC在饮食诱导的肥胖大鼠的脂肪组织中过度表达,并引起3T3-L1脂肪细胞的胰岛素抵抗

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摘要

Secreted protein acidic and rich in cysteine (SPARC) is a secretory multifunctional matricellular glycoprotein. High circulating levels of SPARC have been reported to be associated with obesity and insulin resistance. The aim of the present study was to investigate whether SPARC induces insulin resistance and mitochondrial dysfunction in adipocytes. Our results showed that feeding high fat diet to rats for 12 weeks significantly increased SPARC expression in adipose tissues at both mRNA and protein levels. Moreover, SPARC overexpression in stably transfected 3T3-L1 cells induced insulin resistance and mitochondrial dysfunction, as evidenced by inhibition of insulin-stimulated glucose transport, lower ATP synthesis and mitochondrial membrane potential, reduced expression of glucose transporter 4 (GLUT4), and increased levels of reactive oxygen species (ROS) in mature adipocytes. Finally, overexpression of SPARC also modulated the expression levels of several inflammatory cytokines, which play important roles in insulin resistance, glucose and lipid metabolism during adipogenesis. In conclusion, our data suggest that SPARC is involved in obesity-induced adipose insulin resistance and may serve as a potential target in the treatment of obesity and obesity-related insulin resistance.
机译:分泌的酸性蛋白,富含半胱氨酸(SPARC),是一种分泌型多功能基质细胞糖蛋白。据报道,SPARC的高循环水平与肥胖症和胰岛素抵抗有关。本研究的目的是调查SPARC是否诱导脂肪细胞中的胰岛素抵抗和线粒体功能障碍。我们的结果表明,给大鼠喂高脂饮食12周可显着增加mRNA和蛋白质水平下脂肪组织中SPARC的表达。此外,稳定转染的3T3-L1细胞中SPARC的过表达诱导胰岛素抵抗和线粒体功能异常,这可以通过抑制胰岛素刺激的葡萄糖转运,降低ATP合成和线粒体膜电位,降低葡萄糖转运蛋白4(GLUT4)的表达以及提高水平来证明。脂肪细胞中活性氧(ROS)的分布最后,SPARC的过表达还调节了几种炎症细胞因子的表达水平,这些因子在脂肪生成过程中对胰岛素抵抗,葡萄糖和脂质代谢起着重要作用。总之,我们的数据表明SPARC参与肥胖诱导的脂肪胰岛素抵抗,并且可能成为肥胖和与肥胖相关的胰岛素抵抗治疗的潜在靶标。

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