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作 者:丁红芳[1,2] 丁慧芳[1] 高欣义[1] 伊心浩[1] 鞠秀丽[2]
机构地区:[1]胜利油田中心医院儿科,山东东营257034 [2]山东大学齐鲁医院儿科,山东济南250012
出 处:《基础医学与临床》2013年第9期1186-1190,共5页Basic and Clinical Medicine
摘 要:目的探讨胎盘间充质干细胞(PDMSCs)治疗新生大鼠低氧缺血性脑病(HIBD)的效果及其作用机制。方法HIBD模型乳鼠随机分为对照组、HIBD组、HIBD+PDMSCs治疗组和HIBD+成纤维细胞治疗组。细胞治疗后14 d评估各组生长发育及神经功能,用RT-PCR法和ELISA法检测海马和外周血中TNF-α、IL-17、IFN-γ和IL-10的变化。结果 HIBD组损伤侧大脑明显萎缩、神经行为严重障碍,发育较对照组明显落后(P<0.05),PDMSCs治疗后脑萎缩、神经行为障碍均改善,且幼鼠的体质量显著升高(P<0.05)。细胞治疗后14 d,HIBD组海马和外周血中TNF-α、IL-17和IFN-γ较对照组均升高,而IL-10水平降低(P<0.05);PDMSCs治疗组TNF-α、IL-17、IFN-γ较HIBD组有所降低,而IL-10水平升高(P<0.05)。结论 PDMSCs治疗能够改善新生HIBD大鼠的神经功能和发育,其作用机制可能是通过减轻机体的炎性反应。Objective To investigate the neuroprotective effect of placenta-derived mesenchymal stem cells (PDMSCs) transplantation in rat's hypoxic-ischemic brain damage (HIBD) model and its mechanism. Methods The rats were randomly divided into four groups : sham-operated group ; only HIBD group ; HIBD + PDMSCs-treated group and HIBD + Fibroblasts-treated group. After 2 weeks of treatment, we measured inflammatory cytokines (TNF-α, IFN-γ, IL-IO and IL-17) expression in the brain and serum by appropriate methods. Results Our results indicated that pro-inflammatory cytokine gene and protein expressions increased in the HIBD group, and that PDMSCs-treated group significantly ( all P 〈 0.05 ) lower. Furthermore, PDMSCs treatment was able to increase IL-10. We also observed that motor dysfunctions in fibroblasts-treated group were not improved and the indicators were not statistically significant compared with PDMSCs-treated group. Conclusions PDMSCs treatment plays a critical role in the neuroprotection observed in this model and the mechanism may be partly through alleviating inflammatory reaction.
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