基于NMUR1途径探讨固本防哮饮对哮喘气道慢性炎症中NMU-ILC2s的调控作用

Exploring the Regulatory Effect of Guben Fangxiao Decoction on the NMU-ILC2s Axis in Chronic Airway Inflammation of Asthma Based on the NMUR1 Pathway

  • 摘要:
    目的 研究固本防哮饮对神经调节肽U(NMU)-第二组先天淋巴样细胞(ILC2s)信号通路的调控作用,探讨固本防哮饮改善哮喘气道慢性炎症的可能机制。
    方法 将36只雌性BALB/c小鼠随机分为空白组,模型组,固本防哮饮低、中、高剂量组和孟鲁司特钠组,每组6只。除正常组外,其余组建立哮喘缓解期模型;正常组与模型组给予蒸馏水灌胃,固本防哮饮各剂量组和孟鲁司特钠组按相应剂量灌胃给药,共给药28 d。检测小鼠肺功能,HE染色检测肺组织病理,RT-qPCR检测肺组织中神经调节肽U受体1(NMUR1)、白细胞介素-5(IL-5)、白细胞介素-13(IL-13)、GATA结合蛋白3(GATA-3)等mRNA表达,流式细胞术检测肺组织活化ILC2s细胞比例,钙调神经磷酸酶(CaN)比色法检测酶活力值,免疫荧光检测肺组织切片中NMU、磷酸化细胞外信号调节激酶1/2(p-ERK1/2)+ NMUR1、活化T细胞核因子2(NFAT2)+ NMUR1表达。
    结果 肺功能检测显示,与模型组相比,固本防哮饮低、中、高剂量组和孟鲁司特钠组小鼠Penh值显著降低(P<0.05,P<0.01)。病理学观察显示,与模型组相比,固本防哮饮各剂量组气道及周围炎症细胞浸润程度均得到改善。RT-qPCR结果显示,与模型组相比,固本防哮饮各剂量组NMUR1、IL-5、IL-13 mRNA表达量均明显下调(P<0.01)。流式细胞术显示,与模型组相比,固本防哮饮各剂量组活化型ILC2s比例明显下调(P<0.05,P<0.01)。CaN比色法显示,与模型组相比,固本防哮饮中、高剂量组CaN活力值明显下调(P<0.01)。Western blot显示,与模型组相比,固本防哮饮中、高剂量组和孟鲁司特钠组NMUR1蛋白表达下降(P<0.05,P<0.01)。免疫荧光显示,与模型组相比,固本防哮饮各剂量组NMU明显减少(P<0.05,P<0.01),p-ERK1/2+NMUR1、NFAT2+NMUR1占总NMUR1比例明显减少(P<0.01)。
    结论 固本防哮饮能改善哮喘缓解期模型小鼠2型气道炎症反应,其机制可能与参与调控肺部神经调节肽NMU分泌,从而降低ILC2s膜表面NMUR1表达和调控ILC2s内部p-ERK1/2-CaN-NFAT2信号通路,以此降低ILC2s活化程度有关。

     

    Abstract:
    OBJECTIVE To investigate the regulatory effect of Guben Fangxiao Decoction on the neuromedin U (NMU)–group 2 innate lymphoid cells (ILC2s) signaling pathway, and to explore the potential mechanism by which Guben Fangxiao Decoction alleviates chronic airway inflammation in asthma.
    METHODS Thirty-six female BALB/c mice were randomly assigned to a blank group, a model group, low-, medium-, and high-dose Guben Fangxiao Decoction groups, and a montelukast sodium group, with six mice in each group. Except for the blank group, mice in all groups were used to establish an asthma remission model. The blank and model groups were given distilled water by gavage, while the Guben Fangxiao Decoction groups and the montelukast sodium group received the corresponding drugs by gavage for 28 d. Pulmonary function was assessed, and lung histopathology was evaluated by hematoxylin and eosin (HE) staining. The mRNA expression levels of neuromedin U receptor 1 (NMUR1), interleukin-5 (IL-5), interleukin-13 (IL-13), and GATA-binding protein 3 (GATA-3) in lung tissue were determined by RT-qPCR. The proportion of activated ILC2s in lung tissue was measured by flow cytometry. Calcineurin (CaN) activity was determined using a colorimetric assay. The expression of NMU, phospho-extracellular signal-regulated1/2(p-ERK1/2)+NMUR1, and NFAT2+NMUR1 in lung tissue sections was detected by immunofluorescence staining.
    RESULTS Compared with the model group, Penh values were significantly decreased in the low-, medium-, high-dose Guben Fangxiao Decoction groups and in the montelukast sodium group (P<0.05, P<0.01). Histopathological examination showed that inflammatory cell infiltration in and around the airways was alleviated in all Guben Fangxiao Decoction groups. RT-qPCR analysis demonstrated that the mRNA expression levels of NMUR1, IL-5, and IL-13 were significantly downregulated in all Guben Fangxiao Decoction groups (P<0.01). Flow cytometry showed that the proportion of activated ILC2s was significantly decreased in all Guben Fangxiao Decoction groups compared with the model group (P<0.05, P<0.01). The colorimetric assay showed that CaN activity was significantly decreased in the medium- and high-dose Guben Fangxiao Decoction groups (P<0.01). Western blot analysis showed that compared with the model group, NMUR protein expression was reduced in the medium- and high-dose Guben Fangxiao Decoction groups and the montelukast sodium group (P<0.05, P<0.01). Immunofluorescence analysis revealed that compared with the model group, NMU levels were significantly reduced in all Guben Fangxiao Decoction groups (P<0.05, P<0.01), and the proportions of p-ERK1/2+NMUR1 and NFAT2+NMUR1 relative to total NMUR1 were significantly decreased (P<0.01).
    CONCLUSION Guben Fangxiao Decoction can alleviate type 2 airway inflammation in mice during asthma remission. The underlying mechanism may be associated with regulation of pulmonary NMU secretion, thereby downregulating NMUR1 expression on ILC2s, modulating the intracellular p-ERK1/2 and CaN-NFAT2 signaling pathways, and ultimately suppressing ILC2 activation.

     

/

返回文章
返回