首页|MiR-181a过表达参与调控Treg细胞对儿童变应性鼻炎的机制研究

MiR-181a过表达参与调控Treg细胞对儿童变应性鼻炎的机制研究

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目的:探讨miR-181a在AR儿童血清中的表达,并分析miR-181a对AR患儿Treg细胞分化和功能的调控作用。方法:选择20例AR患儿和20例年龄相近,无过敏史的儿童为研究对象。Pearson相关分析外周血Treg数量与miR-181a表达之间关系。从AR患儿外周血中分离纯化Tregs。将miR-181a模拟物和抑制剂转染到Tregs细胞中。用流式细胞仪和ELISA法评价Tregs的功能。用卵清蛋白建立AR小鼠模型,然后通过功能增益和功能损失法确定miR-181a在AR中的作用。结果:与对照组相比,AR患儿外周血Treg数量减少,并且miR-181a表达显著降低。Pearson相关分析显示外周血Treg数量与 miR-181a表达呈显著正相关(R2=0。335,P<0。001)。miR-181a模拟物促进了 Tregs的增殖,并上调了 IL-10和TGF-β的mRNA表达。荧光素酶报告试验表明,miR-181a直接靶向OPN的3'UTR。在动物实验中,与AR和AR+miR-NC组相比,AR+miR-181a模拟组炎症减轻,AR+miR-181a抑制剂组炎症更严重。重组OPN蛋白显著逆转了 miR-181a模拟物的抗炎作用。此外,AR组小鼠Treg细胞明显减少,miR-181a模拟物显著增加了 AR小鼠的Treg细胞,而重组OPN蛋白显著逆转了miR-181a模拟物诱导的Treg细胞增多。结论:miR-181a的上调显著降低了 OPN的表达,进而减少了嗜酸性粒细胞和增强Treg功能,减轻了 AR发病过程中气道炎症的发生。
The Mechanism Study of miR-181a Overexpression in Regulating Treg Cells in Children Allergic Rhinitis
Objective:To investigate the expression of miR-181a in the serum of AR children and to analyze the regulatory effect of miR-181a on the differentiation and function of Treg cells in AR patients.Methods:Totally,20 children with AR and 20 children of similar age without allergic history were selected as the study subjects.Pearson correlation analysis was used to analyze the relationship between the number of pe-ripheral blood Tregs and miR-181a expression.Tregs were purified from the peripheral blood of AR children.miR-181a mimics and inhibitors were transfected into Tregs cells.The function of Tregs was evaluated by flow cytometry and ELISA.An ovalbumin-induced AR mouse model was established,and then the role of miR-181a in AR was determined by gain-of-function and loss-of-function methods.Results:Compared with the control group,the number of peripheral blood Tregs in AR children was decreased,and the expression of miR-181a was significantly decreased.Pearson correlation analysis showed that the number of peripheral blood Tregs was positively correlated with miR-181a expression(R2=0.335,P<0.001).miR-181a mimics pro-moted the proliferation of Tregs and up-regulated the mRNA expression of IL-10 and TGF-β.Luciferase re-porter assay showed that miR-181a directly targeted the 3'UTR of OPN.In animal experiments,compared with the AR and AR+miR-NC groups,the AR+miR-181a mimic group had less inflammation,and the AR+miR-181a inhibitor group had more severe inflammation.Recombinant OPN protein significantly reversed the anti-inflammatory effect of miR-181a mimics.In addition,the number of Treg cells in AR mice was signifi-cantly decreased,miR-181a mimics significantly increased the number of Treg cells in AR mice,and recom-binant OPN protein significantly reversed the increase of Treg cells induced by miR-181a mimics.Conclu-sion:The up-regulation of miR-181a significantly reduced the expression of OPN,thereby reducing eosino-phils and enhancing Treg function,alleviating the occurrence of airway inflammation during the development of AR.

Allergic rhinitisMiR-181aMiceTregOsteopontin

高旭栋、丁瑜、赵博、张瑾、杨颖

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陕西省人民医院/西安交通大学第三附属医院/西北工业大学附属医院/西安医学院附属医院耳鼻咽喉头颈外科,陕西 西安 710068

变应性鼻炎 MiR-181a 小鼠 Treg 骨桥蛋白

陕西省卫生健康科研项目

201911864

2024

河北医学
河北省医学会

河北医学

CSTPCD
影响因子:1.915
ISSN:1006-6233
年,卷(期):2024.30(7)
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