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Intratracheal administration of adipose derived mesenchymal stem cells alleviates chronic asthma in a mouse model

机译:气管内给予脂肪间充质干细胞可缓解小鼠模型中的慢性哮喘

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Adipose-derived mesenchymal stem cell (ASCs) exerts immunomodulatory roles in asthma. However, the underlying mechanism remains unclear. The present study aimed to explore the effects and mechanisms of ASCs on chronic asthma using an ovalbumin (OVA)-sensitized asthmatic mouse model. Murine ASCs (mASCs) were isolated from male Balb/c mice and identified by the expression of surface markers using flow cytometry. The OVA-sensitized asthmatic mouse model was established and then animals were treated with the mASCs through intratracheal delivery. The therapy effects were assessed by measuring airway responsiveness, performing immuohistochemical analysis, and examining bronchoalveolar lavage fluid (BALF). Additionally, the expression of inflammatory cytokines and lgE was detected by CHIP and ELISA, respectively. The mRNA levels of serum indices were detected using qRT-PCR. The mASCs grew by adherence with fibroblast-like morphology, and showed the positive expression of CD90, CD44, and CD29 as well as the negative expression of CD45 and CD34, indicating that the mASCs were successfully isolated. Administering mASCs to asthmatic model animals through intratracheal delivery reduced airway responsiveness, the number of lymphocytes (P?
机译:脂肪来源的间充质干细胞(ASC)在哮喘中发挥免疫调节作用。但是,其潜在机制仍不清楚。本研究旨在使用卵清蛋白(OVA)致敏的哮喘小鼠模型探讨ASC对慢性哮喘的影响和机制。从雄性Balb / c小鼠中分离出鼠ASC(mASC),并使用流式细胞术通过表面标志物的表达进行鉴定。建立了OVA致敏的哮喘小鼠模型,然后通过气管内递送用mASC处理动物。通过测量气道反应性,进行免疫组织化学分析并检查支气管肺泡灌洗液(BALF)评估治疗效果。另外,分别通过CHIP和ELISA检测炎性细胞因子和IgE的表达。使用qRT-PCR检测血清指标的mRNA水平。 mASC通过遵循成纤维细胞样形态而生长,并显示CD90,CD44和CD29的阳性表达以及CD45和CD34的阴性表达,表明成功分离了mASC。通过气管内给药向哮喘模型动物施用mASC会降低气道反应性,淋巴细胞数量(P 0.01)和lgE(P 0.01),IL-1β(P 0.05),IL-的表达4(P 0.001)和IL-17F(P 0.001),以及血清IL-10和Foxp3水平的升高,以及CD4β+βCD25β+βFoxp3+ Tregs的百分比升高。脾脏,降低IL-17(P 0.05)和RORγ的表达。在OVA致敏哮喘模型中,气管内施用mASC可减轻气道炎症,改善气道重塑并减轻气道高反应性,这可能与mASC还原Th1 / Th2细胞平衡有关。

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