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首页> 外文期刊>Stem cells international >Mechanically Stretched Mesenchymal Stem Cells Can Reduce the Effects of LPS-Induced Injury on the Pulmonary Microvascular Endothelium Barrier
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Mechanically Stretched Mesenchymal Stem Cells Can Reduce the Effects of LPS-Induced Injury on the Pulmonary Microvascular Endothelium Barrier

机译:机械拉伸的间充质干细胞可以减少LPS诱导损伤对肺部微血管内皮屏障的影响

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Mesenchymal stem cells (MSCs) may improve the treatment of acute respiratory distress syndrome (ARDS). However, few studies have investigated the effects of mechanically stretched -MSCs (MS-MSCs) in in vitro models of ARDS. The aim of this study was to evaluate the potential therapeutic effects of MS-MSCs on pulmonary microvascular endothelium barrier injuries induced by LPS. We introduced a cocultured model of pulmonary microvascular endothelial cell (EC) and MSC medium obtained from MSCs with or without mechanical stretch. We found that Wright-Giemsa staining revealed that MSC morphology changed significantly and cell plasma shrank separately after mechanical stretch. Cell proliferation of the MS-MSC groups was much lower than the untreated MSC group; expression of cell surface markers did not change significantly. Compared to the medium from untreated MSCs, inflammatory factors elevated statistically in the medium from MS-MSCs. Moreover, the paracellular permeability of endothelial cells treated with LPS was restored with a medium from MS-MSCs, while LPS-induced EC apoptosis decreased. In addition, protective effects on the remodeling of intercellular junctions were observed when compared to LPS-treated endothelial cells. These data demonstrated that the MS-MSC groups had potential therapeutic effects on the LPS-treated ECs; these results might be useful in the treatment of ARDS.
机译:间充质干细胞(MSCs)可改善急性呼吸窘迫综合征(ARDS)的治疗。然而,很少有研究已经研究了机械拉伸-MSCs(MS-MSCs)在ARDS体外模型中的影响。本研究的目的是评估MS-MSCs对LPS诱导的肺部微血管内皮阻隔损伤的潜在治疗效果。我们介绍了一种来自MSCs的肺部微血管内皮细胞(EC)和MSC培养基的共同化模型,其中没有机械拉伸。我们发现Wright-Giemsa染色显示,MSC形态显着变化,电池血浆在机械拉伸后分别缩小。 MS-MSC基团的细胞增殖远低于未处理的MSC组;细胞表面标记的表达并没有显着变化。与来自未处理的MSC的培养基相比,炎症因子在MS-MSCs的培养基中统计上升高。此外,用来自MS-MSC的培养基恢复用LPS处理的内皮细胞的肺细胞渗透性,而LPS诱导的EC细胞凋亡降低。此外,与LPS处理的内皮细胞相比,观察到对细胞间结的重塑的保护作用。这些数据表明,MS-MSC基团对LPS处理的ECS具有潜在的治疗效果;这些结果可能有助于治疗ARDS。

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