Circ_0070934 promotes MGAT3 expression and inhibits epithelial-mesenchymal transition in bronchial epithelial cells by sponging miR-199a-5p.

IF 2.6 4区 医学 Q2 ALLERGY
Ziqi Ding, Xinru Xiao, Liang Fan, Zhengdao Mao, Chuang Sun, Na Li, Qian Zhang
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引用次数: 0

Abstract

Background: Circular RNA (circRNA) has the potential to serve as a crucial regulator in the progression of bronchial asthma. The objective of this investigation was to elucidate the functional dynamics of the circ_0070934/miR-199a-5p/Mannoside acetylglucosaminyltransferase 3 (MGAT3) axis in the development of asthma.

Methods: Circ_0070934, miR-199a-5p and MGAT3 in peripheral venous blood of 38 asthmatic patients and 43 healthy controls were detected by qRT-PCR, and the expression of MGAT3 protein was examined by ELISA. The GSE148000 dataset was analyzed for differences in MGAT3. The BEAS-2B cells were transfected with circ_0070934 plasmid and small interfering RNA, miR-199a-5p mimics and inhibitors. The apoptosis level was detected by flow cytometry and MGAT3 was detected by qRT-PCR and Western blot. The expression of E-cadherin, N-cadherin, Vimentin was examined by Western blot. Interleukin-4 (IL-4) and IL-13 were used to co-stimulate BEAS-2B cells as an asthmatic airway epithelial cell model. BEAS-2B cells exposed to type 2 cytokines (IL-4 and IL-13) were treated with circ_0070934 plasmid, and the expression of E-cadherin, N-cadherin, and Vimentin was detected by Western blot. The binding relationships were verified using dual-luciferase reporter assay and miRNA pull-down assay.

Results: The expression of circ_0070934 and MGAT3 in peripheral venous blood of asthmatic patients was down-regulated, and the expression of miR-199a-5p was up-regulated. And the expression of MGAT3 was reduced in sputum of asthma patients. Down-regulating the expression of circ_0070934 could promote apoptosis of BEAS-2B cells and increase epithelial-mesenchymal transition (EMT), and this effect can be partially reversed by down-regulating miR-199a-5p. Circ_0070934 could inhibit the process of epithelial mesenchymal transition induced by IL-4 and IL-13 in BEAS-2B cells. In addition, miR-199a-5p could respectively bind to circ_0070934 and MGAT3.

Conclusion: The findings of this study indicate that circ_0070934 may function as a competitive endogenous RNA (ceRNA) of miR-199a-5p, thereby modulating the expression of MGAT3 and impacting the process of EMT in bronchial epithelial cells. These results contribute to the establishment of a theoretical framework for advancing the prevention and treatment strategies for asthma.

Circ_0070934 通过海绵状 miR-199a-5p 促进支气管上皮细胞中 MGAT3 的表达并抑制上皮-间质转化。
背景:环状 RNA(circRNA)可能是支气管哮喘进展过程中的关键调节因子。本研究旨在阐明 circ_0070934/miR-199a-5p/Mannoside acetylglucosaminyltransferase 3 (MGAT3) 轴在哮喘发病过程中的功能动态:通过 qRT-PCR 检测 38 名哮喘患者和 43 名健康对照者外周静脉血中的 Circ_0070934、miR-199a-5p 和 MGAT3,并通过 ELISA 检测 MGAT3 蛋白的表达。GSE148000 数据集分析了 MGAT3 的差异。用 circ_0070934 质粒、小干扰 RNA、miR-199a-5p 模拟物和抑制剂转染 BEAS-2B 细胞。流式细胞仪检测细胞凋亡水平,qRT-PCR 和 Western 印迹检测 MGAT3。通过 Western 印迹检测了 E-cadherin、N-cadherin 和 Vimentin 的表达。用白细胞介素-4(IL-4)和 IL-13 共同刺激 BEAS-2B 细胞作为哮喘气道上皮细胞模型。用 circ_0070934 质粒处理暴露于 2 型细胞因子(IL-4 和 IL-13)的 BEAS-2B 细胞,并通过 Western 印迹检测 E-cadherin、N-cadherin 和 Vimentin 的表达。利用双荧光素酶报告实验和 miRNA 拉取实验验证了两者的结合关系:结果:哮喘患者外周静脉血中 circ_0070934 和 MGAT3 的表达下调,miR-199a-5p 的表达上调。而在哮喘患者的痰液中,MGAT3 的表达有所降低。下调circ_0070934的表达可促进BEAS-2B细胞的凋亡并增加上皮-间质转化(EMT),而下调miR-199a-5p可部分逆转这种效应。Circ_0070934能抑制IL-4和IL-13诱导的BEAS-2B细胞上皮间质转化过程。此外,miR-199a-5p可分别与circ_0070934和MGAT3结合:结论:本研究结果表明,circ_0070934可能是miR-199a-5p的竞争性内源性RNA(ceRNA),从而调节MGAT3的表达,影响支气管上皮细胞的EMT过程。这些结果有助于建立一个理论框架,以推进哮喘的预防和治疗策略。
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来源期刊
CiteScore
4.30
自引率
3.70%
发文量
96
审稿时长
12 weeks
期刊介绍: Allergy, Asthma & Clinical Immunology (AACI), the official journal of the Canadian Society of Allergy and Clinical Immunology (CSACI), is an open access journal that encompasses all aspects of diagnosis, epidemiology, prevention and treatment of allergic and immunologic disease. By offering a high-visibility forum for new insights and discussions, AACI provides a platform for the dissemination of allergy and clinical immunology research and reviews amongst allergists, pulmonologists, immunologists and other physicians, healthcare workers, medical students and the public worldwide. AACI reports on basic research and clinically applied studies in the following areas and other related topics: asthma and occupational lung disease, rhinoconjunctivitis and rhinosinusitis, drug hypersensitivity, allergic skin diseases, urticaria and angioedema, venom hypersensitivity, anaphylaxis and food allergy, immunotherapy, immune modulators and biologics, immune deficiency and autoimmunity, T cell and B cell functions, regulatory T cells, natural killer cells, mast cell and eosinophil functions, complement abnormalities.
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