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Expression Level of MiRNA-126 in Serum Exosomes of Allergic Asthma Patients ai Lung Tissues of Asthmatic Mice

机译:哮喘小鼠的过敏性哮喘患者血清外泌体中miRNA-126的表达水平

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Background: To investigate MiRNA-126 amounts in serum exosomes from allergic asthma patients as well as lung tissues of asthmatic mice, evaluating the expression of its target gene DNMT1 in mouse specimens.Methods: MiRNA-126 amounts in serum exosomes from asthmatic patients were detected by real-time PCR. The mouse model of allergic asthma was established by OVA-sensitization, and allergic symptoms were recorded; serum IL-4 and sIgE level evaluation (ELISA), broncho alveolar lavage fluid (BALF) cell count and H&E staining were performed to assess airway inflammation. MiRNA-126 and DNMT1 levels in the lung of asthmatic and control mice were detected by real-time PCR; DNMT1 protein levels were detected by immunoblot. Results: MiRNA-126 amounts in peripheral blood exosomes from patients with allergic asthma were significantly higher than that of healthy volunteers (P< 0.05). The frequencies of scratching of both sides of the nose and sneezing were elevated within 10 min of excitation in asthmatic rats compared with controls. Meanwhile, OVA-sIgE and IL-4 levels were significantly higher in asthmatic animals than controls (P<0.05). In the asthma group, narrowed bronchial lumen and thickened wall were observed, and bronchial and peripheral vessels showed overt inflammatory cell infiltration. Eosinophil, neutrophil and mast cell amounts in the BALF of asthmatic mice were significantly higher than control values. Furthermore, lung miRNA-126 expression in asthmatic mice was significantly higher than that of controls. Finally, DNMT1 mRNA and protein levels were significantly lower in asthmatic animals compared with controls (P< 0.01). Conclusion: MiRNA-126 is highly expressed in serum exosomes from allergic asthma patients and lung tissues of asthmatic mice, suggesting that it may be involved in the pathogenesis of bronchial asthma.
机译:背景:探讨来自过敏性哮喘患者的血清外泌体以及哮喘小鼠的肺组织的miRNA-126量,评价其靶基因DNMT1在小鼠标本中的表达。方法:检测到来自哮喘患者的血清外泌体的miRNA-126量通过实时PCR。通过OVA致敏建立过敏性哮喘的小鼠模型,并记录过敏症状;进行血清IL-4和SiGe水平评估(ELISA),支气管肺泡灌洗液(BALF)细胞计数和H&E染色以评估气道炎症。通过实时PCR检测哮喘和对照小鼠的肺部肺中的miRNA-126和DNMT1水平;免疫印迹检测DNMT1蛋白水平。结果:来自过敏性哮喘患者的外周血外来血肿的MiRNA-126显着高于健康志愿者(P <0.05)。与对照相比,在哮喘大鼠的激发中,鼻子和打喷嚏两侧的两侧和打喷嚏的频率升高。同时,哮喘动​​物的OVA-SiGe和IL-4水平明显高于对照(P <0.05)。在哮喘组中,观察到狭窄的支气管内腔和增稠的壁,支气管和周围血管显示出明显的炎症细胞浸润。哮喘小鼠BALF中的嗜酸性粒细胞,中性粒细胞和肥大细胞量明显高于控制值。此外,哮喘小鼠中的肺miRNA-126表达明显高于对照物。最后,与对照相比,哮喘动物的DNMT1 mRNA和蛋白质水平显着降低(P <0.01)。结论:MiRNA-126在来自哮喘小鼠的过敏性哮喘患者和肺组织的血清外泌体中高度表达,表明它可能参与支气管哮喘的发病机制。

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