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促红细胞生成素修饰间充质基质细胞移植治疗实验性支气管肺发育不良的时机。

Timing of erythropoietin modified mesenchymal stromal cell transplantation for the treatment of experimental bronchopulmonary dysplasia.

机构信息

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.

出版信息

J Cell Mol Med. 2018 Nov;22(11):5759-5763. doi: 10.1111/jcmm.13843. Epub 2018 Aug 30.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e68/6201357/5509d3c3f57b/JCMM-22-5759-g001.jpg

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