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Mesenchymal Stem Cells Attenuate Renal Fibrosis Through Immune Modulation and Remodeling Properties in a Rat Remnant Kidney Model

机译:间充质干细胞通过大鼠残肾模型中的免疫调节和重塑特性减轻肾纤维化

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摘要

Mesenchymal stem cells (MSCs) have regenerative properties in acute kidney injury, but their role in chronic kidney diseases is still unknown. More specifically, it is not known whether MSCs halt fibrosis. The purpose of this work was to investigate the role of MSCs in fibrogenesis using a model of chronic renal failure. MSCs were obtained from the tibias and femurs of male Wistar-EPM rats. Female Wistar rats were subjected to the remnant model, and 2 vertical bar x vertical bar 10(5) MSCs were intravenously administrated to each rat every other week for 8 weeks or only once and followed for 12 weeks. SRY gene expression was observed in female rats treated with male MSCs, and immune localization of CD73(+)CD90(+) cells at 8 weeks was also assessed. Serum and urine analyses showed an amelioration of functional parameters in MSC-treated animals at 8 weeks, but not at 12 weeks. Masson`s trichrome and Sirius red staining demonstrated reduced levels of fibrosis in MSC-treated animals. These results were corroborated by reduced vimentin, type I collagen, transforming growth factor beta, fibroblast specific protein 1 (FSP-1), monocyte chemoattractant protein 1, and Smad3 mRNA expression and alpha smooth muscle actin and FSP-1 protein expression. Renal interleukin (IL)-6 and tumor necrosis factor alpha mRNA expression levels were significantly decreased after MSC treatment, whereas IL-4 and IL-10 expression levels were increased. All serum cytokine expression levels were decreased in MSC-treated animals. Taken together, these results suggested that MSC therapy can indeed modulate the inflammatory response that follows the initial phase of a chronic renal injury. The immunosuppressive and remodeling properties of MSCs may be involved in the decreased fibrosis in the kidney. STEM CELLS 2009;27:3063-3073
机译:间充质干细胞(MSCs)在急性肾脏损伤中具有再生特性,但在慢性肾脏疾病中的作用仍然未知。更具体地,尚不清楚MSC是否停止纤维化。这项工作的目的是使用慢性肾衰竭模型研究MSC在纤维发生中的作用。从雄性Wistar-EPM大鼠的胫骨和股骨中获得MSC。将雌性Wistar大鼠置于残余模型中,每隔一周每只大鼠静脉注射2根竖条x竖条10(5)MSC,连续8周或仅一次,然后连续12周。在雄性MSC处理的雌性大鼠中观察到SRY基因表达,并评估了8周时CD73(+)CD90(+)细胞的免疫定位。血清和尿液分析显示,经MSC处理的动物在8周时(而非12周时)功能参数得到改善。 Masson的三色和Sirius红染色表明,经MSC处理的动物的纤维化水平降低。这些结果得到波形蛋白,I型胶原蛋白,转化生长因子β,成纤维细胞特异性蛋白1(FSP-1),单核细胞趋化蛋白1和Smad3 mRNA表达以及α平滑肌肌动蛋白和FSP-1蛋白表达降低的证实。 MSC治疗后,肾白细胞介素(IL)-6和肿瘤坏死因子αmRNA表达水平显着降低,而IL-4和IL-10表达水平升高。在MSC治疗的动物中所有血清细胞因子表达水平均降低。综上所述,这些结果表明,MSC治疗确实可以调节慢性肾脏损伤初期的炎症反应。 MSC的免疫抑制和重塑特性可能与肾脏纤维化减少有关。干细胞2009; 27:3063-3073

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