Zhang Ting, Chen Yu-Ting, Shi Jin-Rui, Sun Tian-Tian, Lu Wen-Yi, Xu Kai-Lin, Zeng Ling-Yu
Department of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Department of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China,E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Jun;28(3):1019-1024. doi: 10.19746/j.cnki.issn.1009-2137.2020.03.050.
To investigate the effects of combined infusion of mesenchymal stem cells (MSC) and endothelial progenitor cells (EPC) on lung injury after hematopoietic stem cell transplantation (HSCT).
The experiment was divided into normal control group, irradiation group, bone marrow cell transplantation group (BMT group), BMT+EPC group, BMT+MSC group and BMT+EPC+MSC group. The model of HSCT was established, on the 30th day after transplantation, the mice were sacrificed. Then lung tissue was taken for testing. The mRNA expression levels of VEGF, IL-18, IL-12b were detected by RT-PCR, and protein expression level of NLRP3 was detected by Western blot. The expression of MPO and CD146 was observed by immunohistochemistry assay.
The expression level of VEGF gene in BMT+EPC+MSC group was significantly higher than that in other groups (P<0.01). The expression level of IL-18 and IL-12b gene was the highest in BMT group and the lowest in BMT+EPC+MSC group, and the difference was statistically significant (P<0.05). HSCT could increase the expression of NLRP3 protein, and the BMT+EPC+MSC could significantly reduce the level of NLRP3 protein in lung cells, tending to normal. Compared with normal tissues, the BMT+EPC+MSC could improve the lung tissue structure more effectively, the expression of MPO positive cells was lower, and the expression of VEGF positive cells was higher.
The combined infusion of MSC and EPC can promote capillary regeneration, alleviate inflammation and promote lung repair after HSCT, which is superior to single EPC or MSC infusion.
探讨间充质干细胞(MSC)与内皮祖细胞(EPC)联合输注对造血干细胞移植(HSCT)后肺损伤的影响。
实验分为正常对照组、照射组、骨髓细胞移植组(BMT组)、BMT+EPC组、BMT+MSC组和BMT+EPC+MSC组。建立HSCT模型,移植后第30天处死小鼠,取肺组织进行检测。采用RT-PCR检测VEGF、IL-18、IL-12b的mRNA表达水平,采用Western blot检测NLRP3的蛋白表达水平,采用免疫组织化学法观察MPO和CD146的表达。
BMT+EPC+MSC组VEGF基因表达水平显著高于其他组(P<0.01)。IL-18和IL-12b基因表达水平在BMT组最高,在BMT+EPC+MSC组最低,差异有统计学意义(P<0.05)。HSCT可增加NLRP3蛋白表达,BMT+EPC+MSC可显著降低肺细胞中NLRP3蛋白水平,趋于正常。与正常组织相比,BMT+EPC+MSC能更有效地改善肺组织结构,MPO阳性细胞表达较低,VEGF阳性细胞表达较高。
MSC与EPC联合输注可促进HSCT后毛细血管再生,减轻炎症反应,促进肺修复,优于单一输注EPC或MSC。