Zheng Kai, Wu Weizhen, Yang Shunliang, Huang Lianghu, Chen Jin, Gong Chungui, Fu Zhichao, Lin Ruofei, Tan Jianming
Cell and Organ Transplant Institute, Fuzhou General Hospital, Fuzhou, Fujian 350025, P.R. China.
Radiotherapy Centre, Fuzhou General Hospital, Fuzhou, Fujian 350025, P.R. China.
Exp Ther Med. 2016 Jun;11(6):2425-2431. doi: 10.3892/etm.2016.3248. Epub 2016 Apr 11.
The aim of the present study was to investigate the ability of bone marrow-derived mesenchymal stem cells (BMSCs) to repair radiation-induced acute intestinal injury, and to elucidate the underlying repair mechanism. Male Sprague-Dawley rats were subjected to whole abdominal irradiation using a single medical linear accelerator (12 Gy) and randomly assigned to two groups. Rats in the BMSC-treated group were injected with 1 ml BMSC suspension (2×10 cells/ml) via the tail vein, while the control group rats were injected with normal saline. BMSCs were identified by detecting the expression of CD29, CD90, CD34 and CD45 using flow cytometry. The expression of the cytokines stromal cell-derived factor 1 (SDF-1), prostaglandin E2 (PGE2) and interleukin (IL)-2 was detected using immunohistochemical techniques. Plasma citrulline concentrations were evaluated using an ELISA kit. Rat general conditions, including body weight, and changes in cellular morphology were also recorded. The results suggested that BMSCs exerted a protective effect on radiation-induced acute intestinal injury in rats. The histological damage was rapidly repaired in the BMSC-treated group. In addition, the BMSC-treated group showed significantly reduced radiation injury scores (P<0.01), mildly reduced body weight and plasma citrulline levels, significantly more rapid recovery (P<0.01), significantly reduced expression of the cytokines PGE2 and IL-2 (P<0.05) and significantly increased SDF-1 expression (P<0.01) compared with the control group. In summary, the present results indicate that BMSCs are able to effectively reduce inflammation and promote repair of the structure and function of intestinal tissues damaged by radiation exposure, suggesting that they may provide a promising therapeutic agent.
本研究的目的是探讨骨髓间充质干细胞(BMSCs)修复辐射诱导的急性肠道损伤的能力,并阐明其潜在的修复机制。将雄性Sprague-Dawley大鼠使用单台医用直线加速器进行全腹照射(12 Gy),并随机分为两组。BMSC治疗组的大鼠通过尾静脉注射1 ml BMSC悬液(2×10⁶细胞/ml),而对照组大鼠注射生理盐水。使用流式细胞术通过检测CD29、CD90、CD34和CD45的表达来鉴定BMSCs。使用免疫组织化学技术检测细胞因子基质细胞衍生因子1(SDF-1)、前列腺素E2(PGE2)和白细胞介素(IL)-2的表达。使用ELISA试剂盒评估血浆瓜氨酸浓度。还记录了大鼠的一般状况,包括体重,以及细胞形态的变化。结果表明,BMSCs对辐射诱导的大鼠急性肠道损伤具有保护作用。BMSC治疗组的组织学损伤得到快速修复。此外,与对照组相比,BMSC治疗组的辐射损伤评分显著降低(P<0.01),体重和血浆瓜氨酸水平轻度降低,恢复明显更快(P<0.01),细胞因子PGE2和IL-2的表达显著降低(P<0.05),SDF-1表达显著增加(P<0.01)。总之,目前的结果表明,BMSCs能够有效减轻炎症,并促进受辐射暴露损伤的肠道组织的结构和功能修复,表明它们可能是一种有前景的治疗药物。