BMC Gastroenterology: 间充质干细胞通过抑制小鼠中Toll样受体-4的活性来改善小鼠慢性结肠炎症

2018-09-16 MedSci MedSci原创

目前已知多种肠外表现(EIM)包括肝胆并发症,都与与炎性肠病(IBD)有关。也有报道显示间充质干细胞(MSC)移植在IBD的治疗中发挥有潜在的疗效。因此,本研究旨在探讨间充质干细胞(MSC)在使用硫酸葡聚糖钠(DSS)诱导的小鼠慢性结肠炎模型的改善作用。

背景
目前已知多种肠外表现(EIM)包括肝胆并发症,都与与炎性肠病(IBD)有关。也有报道显示间充质干细胞(MSC)移植在IBD的治疗中发挥有潜在的疗效。因此,本研究旨在探讨间充质干细胞(MSC)在使用硫酸葡聚糖钠(DSS)诱导的小鼠慢性结肠炎模型的改善作用。

方法
研究人员先建立DSS诱导的小鼠慢性结肠炎模型,并用MSC治疗。采用疾病活动指数(DAI),体重(BW),结肠长度和组织病理学来评估结肠炎的严重程度。通过细胞裂解物测试(LAL-测试)检测血清脂多糖(LPS)水平。同时对小鼠的组织学和肝功能进行相关检测。研究人员同时对血清LPS水平和肠系膜淋巴结(MLN)的细菌移位进行了分析。本项研究中定义的促炎细胞因子包括肿瘤坏死因子-α(TNF-α),干扰素-γ(IFN-γ),白细胞介素-1β(IL-1β),白细胞介素-17A(IL-17A),Toll受体4(TLR4),并分别用免疫组化染色,免疫印迹分析和实时荧光定量PCR检测TNF受体相关因子6(TRAF6)和核因子κB(NF-κB)的浓度。

结果
DSS诱导的慢性结肠炎小鼠模型的特征表现在于BW减少,DAI升高,组织学炎症恶化,以及高水平的LPS和大肠杆菌易位。DSS给药后研究人员观察到小鼠肝脏组织出现病理学损伤,肝功能受损,蛋白质和TNF-α,IFN-γ,IL-1β,IL-17A,TLR4,TRAF6和NF-κB的mRNA水平升高。对小鼠进行MSCs移植后,MSCs通过降低LPS水平,降低TNF-α,IFN-γ,IL-1β,IL-17A,TLR4,TRAF6和NF-κB的蛋白和mRNA表达,显着改善了结肠和肝脏的病理的表现。

结论
MSCs可通过LPS / TLR4途径抑制肠源性内毒素血症和肝脏炎症,改善慢性结肠炎相关肝胆并发症。MSCs将来可能会成为慢性结肠炎相关肝胆并发症的新型治疗方法。

原始出处:

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    2018-09-17 kafei

    学习了谢谢

    0

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