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Mesenchymal stem cells transplantation ameliorates glomerular injury in streptozotocin-induced diabetic nephropathy in rats via inhibiting oxidative stress

机译:间充质干细胞移植通过抑制氧化应激改善链脲佐菌素诱导的糖尿病性肾病大鼠肾小球损伤

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Aims: Mesenchymal stem cells (MSCs) have been demonstrated to be protective in diabetic nephropathy (DN) by reducing albuminuria and attenuating glomerular injury. However, the mechanisms remain unclear. The aim of this study was to explore the effects of MSCs on oxidative stress in DN. Materials/methods: Streptozotocin-induced diabetic rats received no treatment or treatment with MSCs (2×106, via tail vein) for two continuous weeks. Two other control groups received the antioxidant-probucol or insulin. Eight weeks after treatment, physical, biochemical, renal functional and morphological parameters were measured. Glomerular mesangial cells were cultured for the in vitro experiment. Results: Green fluorescent protein-labeled MSCs were only detected around the glomeruli and near vessels in the kidney. MSCs treatment dramatically reduced blood glucose, urinary albumin excretion, creatinine clearance and renal mass index. The glomerulosclerosis as revealed by periodic acid Schiff staining and expression of collagen I and fibronectin was significantly reduced by MSC treatment. Oxidative stress was also markedly inhibited in the MSCs group. Furthermore, the expression of TGF-β and membrane localization of GLUT1 were also down-regulated by MSCs. MSCs secreted a significant amount of hepatocyte growth factor (HGF). In vitro, MSC conditioned medium inhibited up-regulation of TGF-β expression stimulated by high glucose and HGF neutralizing antibody blocked the inhibitory effect of MSC conditioned medium. Conclusions: MSC treatment reduced urinary albumin excretion and ameliorated glomerulosclerosis. The mechanisms underlying these effects involved reduced blood glucose levels and cellular glucose uptake mediated by GLUT1, thus inhibiting oxidative stress.
机译:目的:间充质干细胞(MSC)已被证明可通过减少白蛋白尿和减轻肾小球损伤来保护糖尿病性肾病(DN)。但是,机制尚不清楚。这项研究的目的是探讨MSC对DN氧化应激的影响。材料/方法:链脲佐菌素诱导的糖尿病大鼠连续两周未接受任何治疗或用MSC(2×106,经尾静脉)治疗。另外两个对照组接受抗氧化剂-普罗布考或胰岛素。治疗八周后,测量身体,生化,肾功能和形态参数。培养肾小球系膜细胞用于体外实验。结果:仅在肾小球周围和血管附近检测到绿色荧光蛋白标记的MSC。 MSCs治疗可显着降低血糖,尿白蛋白排泄,肌酐清除率和肾脏质量指数。高碘酸席夫氏染色显示的肾小球硬化和胶原I和纤连蛋白的表达通过MSC处理显着降低。 MSCs组的氧化应激也被显着抑制。此外,MSCs也下调了TGF-β的表达和GLUT1的膜定位。 MSC分泌了大量的肝细胞生长因子(HGF)。在体外,MSC条件培养基抑制了高葡萄糖刺激的TGF-β表达的上调,而HGF中和抗体阻断了MSC条件培养基的抑制作用。结论:MSC治疗可减少尿白蛋白排泄并改善肾小球硬化。这些作用的潜在机制涉及降低血糖水平和由GLUT1介导的细胞葡萄糖摄取,从而抑制氧化应激。

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