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Bone marrow-derived mesenchymal stem cells protect against lung injury in a mouse model of bronchopulmonary dysplasia

机译:骨髓源性间充质干细胞在支气管肺发育不良的小鼠模型中预防肺损伤

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摘要

The aim of the present study was to investigate the effect of bone marrow-derived mesenchymal stem cells (BMSCs) in the treatment of lung injury in a mouse model of bronchopulmonary dysplasia (BPD) and examine the underlying mechanisms. A mouse model of BPD was created using continuous exposure to high oxygen levels for 14 days. BMSCs were isolated, cultured and then labeled with green fluorescent protein. Cells (1x10(6)) were subsequently injected intravenously 1 h prior to high oxygen treatment. Animals were randomly divided into three groups (n=5 in each): Control group, BPD model group and BMSC injection group. At two weeks post-treatment, the expression of transforming growth factor-beta 1 (TGF-beta 1), vascular endothelial growth factor (VEGF) and von Willebrand factor (vWF) was detected using immunohistochemical staining and immunofluorescence. Compared with the BPD model group, the body weight, airway structure and levels of TGF-beta 1 and VEGF were significantly improved in the BMSC-treated group. Immunofluorescence observations indicated that BMSCs were able to differentiate into cells expressing vWF and VEGF, which are markers of vascular tissues. The present study demonstrated that intravenous injection of BMSCs significantly improved lung damage in a neonatal mouse model of BPD at 14 days following hyperoxia-indueed injury. This provides novel information which may be used to guide further investigation into the use of stem cells in BPD.
机译:本研究的目的是在支气管肺发育不良(BPD)小鼠模型中研究骨髓来源的间充质干细胞(BMSC)在治疗肺损伤中的作用并探讨其潜在机制。通过连续暴露于高氧水平14天来创建BPD小鼠模型。分离,培养BMSC,然后用绿色荧光蛋白标记。随后在高氧治疗前1小时静脉内注射细胞(1x10(6))。将动物随机分为三组(每组n = 5):对照组,BPD模型组和BMSC注射组。在治疗后两周,使用免疫组织化学染色和免疫荧光检测转化生长因子-β1(TGF-β1),血管内皮生长因子(VEGF)和血管性血友病因子(vWF)的表达。与BPD模型组相比,BMSC治疗组的体重,气道结构以及TGF-β1和VEGF的水平均有明显改善。免疫荧光观察表明,BMSCs能够分化成表达vWF和VEGF的细胞,而vWF和VEGF是血管组织的标志物。本研究表明,在高氧血症引起的损伤后第14天,静脉注射BMSC可以显着改善BPD新生小鼠模型的肺损伤。这提供了新颖的信息,可用于指导进一步研究BPD中干细胞的使用。

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