Notch配体Jagged1和Delta4在慢性哮喘小鼠模型中Th17/Treg免疫失衡中的作用。

IF 1.5 4区 医学 Q3 RESPIRATORY SYSTEM
Experimental Lung Research Pub Date : 2021-05-01 Epub Date: 2021-06-07 DOI:10.1080/01902148.2021.1933653
Zhen He, Jirong Wu, Xiaoli Zeng, Hairong Bao, Xiaoju Liu
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引用次数: 6

摘要

目的:哮喘与T辅助细胞(Th)17/调节性T细胞(Treg)免疫失衡有关,其中Notch信号通路起着至关重要的作用。本研究旨在探讨Notch配体Jagged1和Delta4在慢性哮喘小鼠Th17/Treg免疫失衡中的作用。方法:实验动物被随机分配到生理盐水、卵清蛋白(OVA)和OVA + γ-分泌酶抑制剂(GSI)组。通过OVA致敏和激发诱导慢性哮喘小鼠模型。GSI在OVA激发前在OVA中腹膜内注射 + GSI集团。肺功能、肺组织病理学和免疫组织化学以评估气道炎症,酶联免疫吸附测定以测量细胞因子水平,流式细胞术以测量CD4+T细胞中Th17(Th17%)和Treg%的比例,定量实时聚合酶链式反应和western印迹以测量肺组织中Jagged1和Delta4的mRNA和蛋白水平,并进行相关分析。结果:慢性哮喘小鼠的肺功能和组织病理学以及支气管肺泡灌洗液(BALF)中的IL-4、IL-13和IFN-γ水平显示出哮喘的特征性变化。OVA组的Th17%、Th17/Treg比率、BALF和血清IL-17水平以及IL-17/IL-10比率显著增加,而Treg%和IL-10水平显著降低。Jagged1和Delta4的mRNA和蛋白表达水平显著增加。GSI可降低慢性哮喘小鼠Th17%、Th17/Treg比率、IL-17、IL-17/IL-10比率和Jagged1的表达。在OVA组中,Jagged1和Delta4的mRNA和蛋白水平与Th17/Treg比率呈正相关,而在OVA中,只有Jagged 1的mRNA和蛋白质水平与Th17-Treg比率正相关 + GSI集团。结论:在慢性哮喘小鼠中,Th17/Treg比例增加,Notch配体Jagged1和Delta4过度活跃,并正调节Th17/Treg+失衡。GSI部分抑制Jagged1并缓解Th17/Treg失衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of the Notch ligands Jagged1 and Delta4 in Th17/Treg immune imbalance in a mouse model of chronic asthma.

Purpose: Asthma is associated with a T helper (Th)17/regulatory T (Treg) cells immune imbalance where the Notch signaling pathway contributes vitally. This study aimed to explore the role of Notch ligands Jagged1 and Delta4 in the Th17/Treg immune imbalance of chronic asthmatic mice.

Methods: The experimental animals were randomly assigned to the Saline, ovalbumin (OVA), and OVA + γ-secretase inhibitor (GSI) groups. A mouse model of chronic asthma was induced by OVA sensitization and challenge. GSI was injected intraperitoneally before the OVA challenge in the OVA + GSI group. Lung function, lung histopathology and immunohistochemistry to assess airway inflammation, enzyme-linked immunosorbent assay to measure cytokines levels, flow cytometry to measure the proportions of Th17 (Th17%) and Treg% in CD4+T cells, quantitative real-time polymerase chain reaction and western blot to measure mRNA and protein levels of Jagged1 and Delta4 in lung tissue, and correlation analysis were performed.

Results: Lung function and histopathology and IL-4, IL-13, and IFN-γ levels in the bronchoalveolar lavage fluid (BALF) of chronic asthmatic mice showed characteristic changes of asthma. The Th17%, Th17/Treg ratio, BALF and serum IL-17 levels, and IL-17/IL-10 ratio increased significantly in the OVA group, while the Treg% and IL-10 level significantly decreased. mRNA and protein expression levels of Jagged1 and Delta4 increased significantly. GSI could reduce the Th17%, Th17/Treg ratio, IL-17, IL-17/IL-10 ratio, and Jagged1 expression in chronic asthmatic mice. The mRNA and protein levels of Jagged1 and Delta4 were positively correlated with the Th17/Treg ratio in the OVA group, while only those of Jagged1 were positively correlated with the Th17/Treg ratio in the OVA + GSI group.

Conclusions: In chronic asthmatic mice, the Th17/Treg ratio increased, and the Notch ligands Jagged1 and Delta4 were overactive and positively regulated the Th17/Treg imbalance. GSI partially inhibited Jagged1 and relieved the Th17/Treg imbalance.

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来源期刊
Experimental Lung Research
Experimental Lung Research 医学-呼吸系统
CiteScore
3.80
自引率
0.00%
发文量
23
审稿时长
2 months
期刊介绍: Experimental Lung Research publishes original articles in all fields of respiratory tract anatomy, biology, developmental biology, toxicology, and pathology. Emphasis is placed on investigations concerned with molecular, biochemical, and cellular mechanisms of normal function, pathogenesis, and responses to injury. The journal publishes reports on important methodological advances on new experimental modes. Also published are invited reviews on important and timely research advances, as well as proceedings of specialized symposia. Authors can choose to publish gold open access in this journal.
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