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Hepatic protein tyrosine phosphatase receptor gamma links obesity-induced inflammation to insulin resistance

机译:肝蛋白酪氨酸磷酸酶受体γ将肥胖引起的炎症与胰岛素抵抗联系起来

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Obesity-induced inflammation engenders insulin resistance and type 2 diabetes mellitus (T2DM) but the inflammatory effectors linking obesity to insulin resistance are incompletely understood. Here, we show that hepatic expression of Protein Tyrosine Phosphatase Receptor Gamma (PTPR-γ) is stimulated by inflammation in obese/T2DM mice and positively correlates with indices of inflammation and insulin resistance in humans. NF-κB binds to?the promoter?of?Ptprg and is required for inflammation-induced PTPR-γ expression. PTPR-γ loss-of-function lowers glycemia and insulinemia by enhancing insulin-stimulated suppression of endogenous glucose production. These phenotypes are rescued by re-expression of Ptprg only in liver of mice lacking Ptprg globally. Hepatic PTPR-γ overexpression that mimics levels found in obesity is sufficient to cause severe hepatic and systemic insulin resistance. We propose hepatic PTPR-γ as a link between obesity-induced inflammation and insulin resistance and as potential target for treatment of T2DM.
机译:肥胖引起的炎症会引起胰岛素抵抗和2型糖尿病(T2DM),但是将肥胖与胰岛素抵抗联系起来的炎症效应尚未得到完全了解。在这里,我们显示,肥胖/ T2DM小鼠的炎症刺激了蛋白酪氨酸磷酸酶受体γ(PTPR-γ)的肝表达,并且与人的炎症指数和胰岛素抵抗呈正相关。 NF-κB与Ptprg的“启动子”结合,是炎症诱导的PTPR-γ表达所必需的。 PTPR-γ功能丧失通过增强胰岛素刺激的内源性葡萄糖生成的抑制作用来降低血糖和胰岛素血症。仅在全球缺乏Ptprg的小鼠肝脏中通过Ptprg的重新表达来挽救这些表型。模仿肥胖症中发现的肝PTPR-γ过表达足以引起严重的肝和全身胰岛素抵抗。我们建议将肝脏PTPR-γ作为肥胖引起的炎症和胰岛素抵抗之间的联系,并作为治疗T2DM的潜在靶点。

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