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γ-促分泌酶抑制剂对毛细支气管炎模型大鼠体内 Th17细胞分化的影响

王海英 刘良宵 吴福玲 高萌

中国免疫学杂志2016,Vol.32Issue(12):1765-1768,4.
中国免疫学杂志2016,Vol.32Issue(12):1765-1768,4.DOI:10.3969/j.issn.1000-484X.2016.12.008

γ-促分泌酶抑制剂对毛细支气管炎模型大鼠体内 Th17细胞分化的影响

Affection to differentiation of Th17 cell in bronchiolitis rat models after injectingγ-secretase inhibitor

王海英 1刘良宵 1吴福玲 1高萌1

作者信息

  • 1. 滨州医学院,烟台 264003
  • 折叠

摘要

Abstract

Objective:To investigate the affection to the differentiation of Th17 cell in rat models of bronchiolitis after blocking Notch signaling by γ-secretase inhibitor and provide rationale to seek new target for bronchiolitis drug treatment. Methods:The rats were randomly divided into normal group,bronchiolitis group andγ-secretase inhibitor group. The model of bronchiolitis was established successfully by nasal dripping,and γ-secretase inhibitor(MW167) was injected into the vena caudalis. The pathological changes of the airway were observed by HE staining;the plasma level of interleukin17 ( IL-17 ) was detected by ELISA;the level of RORγt mRNA in lung tissues and peripheral blood mononuclear cells( PBMCs) was tested by real-time quantitative PCR;the levels of Notch signaling and RORγt protein in lung tissues were examined by Western blot. Results:Compared to the bronchiolitis group, the histopathologic change in MW167 intravenous injection group was significantly alleviated;the plasma level of IL-17 was decreased;the level of RORγt mRNA in lung tissues and PBMCs was lower in MW167-treated group than bronchiolitis group;the levels of Notch signaling and RORγt were decreased. Conclusion:γ-secretase inhibitor through intravenous injection suppresses the differentiation of Th17 cell and relieves the airway inflammation of bronchiolitis in rat models after blocking Notch signaling and has potential therapeutic value for treating bron-chiolitis.

关键词

毛细支气管炎/Notch/γ-促分泌酶抑制剂/Th17细胞

Key words

Bronchiolitis/Notch/γ-secretase inhibitor/Th17 cell

分类

医药卫生

引用本文复制引用

王海英,刘良宵,吴福玲,高萌..γ-促分泌酶抑制剂对毛细支气管炎模型大鼠体内 Th17细胞分化的影响[J].中国免疫学杂志,2016,32(12):1765-1768,4.

基金项目

本文受山东省自然科学基金(ZR2014HL001)和山东省医药卫生科技发展计划项目(2013WS0312)资助。 (ZR2014HL001)

中国免疫学杂志

OA北大核心CSCDCSTPCD

1000-484X

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