Department of Pediatrics, The Second Hospital of Shandong University, Jinan, China.
Central Research Laboratory, Institute of Medical Science, The Second Hospital of Shandong University, Jinan, China.
J Cell Mol Med. 2018 Nov;22(11):5759-5763. doi: 10.1111/jcmm.13843. Epub 2018 Aug 30.
The aim of this study is to optimize the timing of erythropoietin gene modified mesenchymal stem cells (EPO-MSCs) transplantation for bronchopulmonary dysplasia (BPD). Three weeks post-operation, the results indicated that the damage of airway structure and apoptosis were significantly decreased, the proliferation was increased in three EPO-MSCs transplantation groups as compared with BPD mice. Moreover, the inflammation cytokines were improvement in early EPO-MSCs injection mice than in BPD mice, but there was no significant difference between late injection and BPD groups. Furthermore, the protein expression ratio of p-p38/p38MAPK was down-regulation in early mice but not in late transplantation mice. Our findings suggest that EPO-MSCs maybe attenuate BPD injury in early than in late administration by inhibiting inflammation response through down-regulation of the p38MAPK signalling pathway.
本研究旨在优化促红细胞生成素基因修饰间充质干细胞(EPO-MSCs)移植治疗支气管肺发育不良(BPD)的时机。术后 3 周,结果表明,与 BPD 小鼠相比,EPO-MSCs 移植组的气道结构损伤和细胞凋亡明显减少,增殖增加。此外,早期 EPO-MSCs 注射组的炎症细胞因子水平改善优于 BPD 组,但晚期注射组与 BPD 组之间无显著差异。此外,早期组的 p-p38/p38MAPK 蛋白表达比值下调,而晚期移植组则无此变化。我们的研究结果表明,EPO-MSCs 可能通过下调 p38MAPK 信号通路抑制炎症反应,在早期治疗中减轻 BPD 损伤,而不是在晚期治疗中。