...
首页> 外文期刊>Cell metabolism >PGRN is a key adipokine mediating high fat diet-induced insulin resistance and obesity through IL-6 in adipose tissue
【24h】

PGRN is a key adipokine mediating high fat diet-induced insulin resistance and obesity through IL-6 in adipose tissue

机译:PGRN是通过脂肪组织中的IL-6介导高脂饮食诱导的胰岛素抵抗和肥胖症的主要脂肪因子

获取原文
获取原文并翻译 | 示例
           

摘要

Adipose tissue secretes adipokines that mediate insulin resistance, a characteristic feature of obesity and type 2 diabetes. By differential proteome analysis of cellular models of insulin resistance, we identified progranulin (PGRN) as an adipokine induced by TNF-α and dexamethasone. PGRN in blood and adipose tissues was markedly increased in obese mouse models and was normalized with treatment of pioglitazone, an insulin-sensitizing agent. Ablation of PGRN (Grn -/-) prevented mice from high fat diet (HFD)-induced insulin resistance, adipocyte hypertrophy, and obesity. Grn deficiency blocked elevation of IL-6, an inflammatory cytokine, induced by HFD in blood and adipose tissues. Insulin resistance induced by chronic administration of PGRN was suppressed by neutralizing IL-6 in vivo. Thus, PGRN is a key adipokine that mediates HFD-induced insulin resistance and obesity through production of IL-6 in adipose tissue, and may be a promising therapeutic target for obesity.
机译:脂肪组织分泌介导胰岛素抵抗的肥胖因子,肥胖和2型糖尿病的特征之一。通过胰岛素抵抗细胞模型的差异蛋白质组分析,我们确定了颗粒蛋白(PGRN)是由TNF-α和地塞米松诱导的脂肪因子。在肥胖小鼠模型中,血液和脂肪组织中的PGRN显着增加,并通过胰岛素增敏剂吡格列酮治疗使其正常化。 PGRN(Grn-/-)的消融可防止小鼠遭受高脂饮食(HFD)诱导的胰岛素抵抗,脂肪细胞肥大和肥胖。 Grn缺乏会阻止血液和脂肪组织中HFD诱导的炎性细胞因子IL-6升高。通过体内中和IL-6抑制了PGRN的长期给药所诱导的胰岛素抵抗。因此,PGRN是通过脂肪组织中IL-6的产生介导HFD诱导的胰岛素抵抗和肥胖的关键脂肪因子,并且可能是肥胖的有希望的治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号