实验研究

NF-κB在变应性鼻炎发病中的调节作用

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  • 莆田学院基础医学院解剖生理学教研室,  福建   莆田   351100
张敏(1969-),男,福建莆田人,博士,教授,研究方向:变应性疾病发病机制及干预治疗,Tel:(0564)2768812,E-mail:zm5995@sina.com

收稿日期: 2019-03-13

  网络出版日期: 2019-08-01

基金资助

莆田学院育苗基金资助课题(2014058;2016111);国家自然青年基金(81502360)

Role of NF-κB in pathogenesis of allergic rhinitis

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  • Department of Anatomy and Physiology, Basic Medical College of Putian University, Putian 351100, Fujian Province, China

Received date: 2019-03-13

  Online published: 2019-08-01

摘要

目的 探讨变应性鼻炎(allergic rhinitis,AR)病理过程中TLR-NF-κB信号传导通路的调节机制及核因子-κB(NF-κB)对嗜酸性粒细胞聚集的调节作用。  方法 50只大鼠随机分成A组(对照组)、B组(AR组)、C组(AR+PGN)、D组(AR+PGN+Pam3CSK4)、E组(AR+PGN+BEL),应用卵清蛋白建造AR模型,HE染色观察鼻黏膜形态改变并计数炎症细胞浸润数,ELISA法检测鼻腔清洗液IFN-γ、IL-4、嗜酸性粒细胞主要碱性蛋白(MBP)及IgE的含量,Real-Time PCR及Western blot法检测Toll样受体2(TLR2)、NF-κB的表达情况。  结果    B组变应性损伤明显,鼻黏膜嗜酸性粒细胞浸润数多于其他组,IL-4、MBP及IgE的表达较A组增高(P<0.05);C组鼻黏膜以中性粒细胞浸润为主,IFN-γ、TLR2及NF-κB的表达较B组增高(P<0.05);D、E组炎症细胞浸润数、IL-4、MBP及IgE的表达较B组降低(P<0.05)。  结论 调控TLR-NF-κB传导通路的表达即抑制NF-κB的过度表达,有利于调节变应性鼻炎病理过程中嗜酸性粒细胞的增值聚集。

本文引用格式

张敏, 吴聃, 刘黎星, 侯赛榕, 蔡丽希 . NF-κB在变应性鼻炎发病中的调节作用[J]. 中国临床解剖学杂志, 2019 , 37(4) : 421 -424 . DOI: 10.13418/j.issn.1001-165x.2019.04.012

Abstract

Objective To experimentally investigate a potential mechanism of the TLR-NF-κB signaling pathway in the pathogenesis of allergic rhinitis (AR), and the role of NF-κB in eosinophil aggregation. Methods A total of 50 rats were randomly divided into five groups with A (control group), B (AR group), C (group of AR+PGN), D (group of AR+PGN+Pam3CSK4), and E (group of AR +PGN+BEL). AR model was established with ovalbumin. Hematoxylin and eosin (H&E) staining was used to detect the morphologic change of nasal mucosa and count the number of infiltrated inflammatory cell. The contents of IFN-γ, IL-4, MBP and IgE in nasal cleanser were detected by ELISA. Expression of NF-κB and TLR2 was measured by Real-Time polymerase chain reaction (PCR) and Western blot. Results Obvious allergic injury was observed in AR rats (B group). The number of infiltrated eosinophils in nasal mucosa in group B was higher than in other groups. The expressions of IL-4, MBP and IgE in group B were higher than in group A (P<0.05). Neutrophil infiltration was predominant in nasal mucosa of group C, and the expression of IFN-γ, TLR2 and NF-κB was higher in group B (P<0.05). Inflammatory cell infiltration, IL-4, MBP and IgE expression in group D and E were lower than in group B (P<0.05). Conclusions Regulating the expression of TLR-NF-κB pathway and inhibiting the over-expression of NF-κB is beneficial to regulating the aggregation of eosinophils in the pathogenesis of allergic rhinitis.

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