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Angiotensin II- and glucose-stimulated extracellular matrix production: mediation by the insulin-like growth factor (IGF) axis in a murine mesangial cell line

机译:血管紧张素II和葡萄糖刺激的细胞外基质产生:在小鼠系膜细胞系中由胰岛素样生长因子(IGF)轴介导

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In diabetic nephropathy, glomerular mesangial cells exhibit aberrant anabolic activity that includes excessive production of extracellular matrix (ECM) proteins, leading to crowding of filtration surface areas and possible renal failure. In the present study, a murine mesangial cell line (MES-13 cells) was studied to determine the roles of the renin-angiotensin system (RAS) and the insulin-like growth factor (IGF) axis in the anabolic response to elevated glucose levels. Culture of MES-13 cells in medium containing supra-physiological glucose concentrations (>5.5 mmol/l) resulted in increased production of ECM proteins including laminin, fibronectin, and heparan sulfate proteoglycan with concurrent increases in IGF-binding protein (IGFBP)-2 production. These responses were blocked by the angiotensin receptor antagonists saralasin and losartan, while exogenous angiotensin II (Ang II) treatment directly stimulated increases in ECM and IGFBP-2. In all experiments, IGFBP-2 levels were correlated with anabolic activity implicating IGFBP-2 as a possible mediator in cellular responses to high glucose and Ang II. Such mediation appears to involve IGFBP-2 modulation of IGF-I signaling, since all responses to high glucose or Ang II were blocked by immuno-neutralization of IGF-I. These data suggest alterations in the IGF axis as key mechanisms underlying nephropathic responses of mesangial cells to Ang II and high glucose.
机译:在糖尿病性肾病中,肾小球系膜细胞表现出异常的合成代谢活性,其中包括细胞外基质(ECM)蛋白的过量产生,导致滤过表面区域拥挤和可能的肾衰竭。在本研究中,研究了鼠系膜细胞系(MES-13细胞),以确定肾素-血管紧张素系统(RAS)和胰岛素样生长因子(IGF)轴在合成代谢对葡萄糖水平升高的反应中的作用。在含有超生理葡萄糖浓度(> 5.5 mmol / l)的培养基中培养MES-13细胞会导致ECM蛋白(包括层粘连蛋白,纤连蛋白和硫酸乙酰肝素蛋白聚糖)的产生增加,同时IGF结合蛋白(IGFBP)-2也会增加生产。这些反应被血管紧张素受体拮抗剂saralasin和losartan阻断,而外源性血管紧张素II(Ang II)治疗直接刺激了ECM和IGFBP-2的增加。在所有实验中,IGFBP-2水平与合成代谢活性相关,这暗示IGFBP-2可能是细胞对高葡萄糖和Ang II反应的介导因子。这种介导似乎涉及IGF-1信号转导的IGFBP-2调节,因为对高葡萄糖或Ang II的所有应答均被IGF-1的免疫中和作用所阻断。这些数据表明,IGF轴的改变是肾小球系膜细胞对Ang II和高血糖肾病反应的关键机制。

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