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环状RNA-0001454通过吸附miR-770-5p并调控cbl-b减轻哮喘气道炎症和重塑

circ-0001454 alleviates asthma airway inflammation and remodeling via sponging miR-770-5p and regulating cbl-b.

作者信息

Liu Ruobai, Song Yilan, Wang Zhiguang, Dai Longzhu, Bai Qiaoyun, Li Yan, Piao Hongmei, Wang Chongyang, Yan Guanghai

机构信息

Jilin Key Laboratory for Immune and Targeting Research on Common Allergic Diseases, Yanbian University, Yanji, China.

Department of Anatomy, Histology and Embryology, Yanbian University Medical College, Yanji, China.

出版信息

Front Cell Dev Biol. 2025 Apr 8;13:1566223. doi: 10.3389/fcell.2025.1566223. eCollection 2025.

Abstract

Bronchial asthma is a chronic inflammatory disease that has long been a severe threat to human physical and mental health. Circular RNAs (circRNAs) and microRNAs (miRNAs) are involved in regulating various processes in asthma. However, the mechanisms by which these molecules influence the pathophysiological processes of asthma through target gene regulation remain unclear. Our study found that inhibition of miR-770-5p alleviated airway inflammation and remodeling in asthmatic mice. Furthermore, bioinformatics analysis revealed that circ-0001454 harbors binding sites for miR-770-5p, acting as a sponge to adsorb miR-770-5p and function as a competing endogenous RNA (ceRNA), thereby negatively regulating the expression of miR-770-5p. Circ-0001454 not only alleviated airway inflammation and remodeling in asthmatic mice, but also participated in modulating the HDM-induced inflammatory response in BEAS-2B cells. It mitigated bronchial epithelial cell inflammatory damage, reduced oxidative stress, apoptosis, and mitochondrial membrane potential loss. Mechanistically, we observed that circ-0001454 partially alleviated the inflammatory damage of epithelial cells caused by miR-770-5p overexpression excessive reactive oxygen species (ROS) production, apoptosis, and mitochondrial membrane potential disruption. Lastly, we found that circ-0001454 targets miR-770-5p and participates in regulating the expression of cbl-b, which in turn modulates the levels of EGFR, AKT1, and MAPK1 proteins, thereby alleviating inflammation in airway epithelial cells. These findings reveal the role of miR-770-5p in asthma, and how circ-0001454, by binding to miR-770-5p and targeting the gene cbl-b, contributes to the attenuation of airway inflammation, reduction of ROS levels, inhibition of apoptosis, and restoration of mitochondrial membrane potential. This regulation of cbl-b, EGFR, AKT1, and MAPK1 suggests new potential therapeutic targets for asthma treatment.

摘要

支气管哮喘是一种慢性炎症性疾病,长期以来一直严重威胁着人类的身心健康。环状RNA(circRNAs)和微小RNA(miRNAs)参与调节哮喘的各种过程。然而,这些分子通过靶基因调控影响哮喘病理生理过程的机制仍不清楚。我们的研究发现,抑制miR-770-5p可减轻哮喘小鼠的气道炎症和重塑。此外,生物信息学分析显示,circ-0001454含有miR-770-5p的结合位点,可作为海绵吸附miR-770-5p,并作为竞争性内源RNA(ceRNA)发挥作用,从而负向调节miR-770-5p的表达。Circ-0001454不仅减轻了哮喘小鼠的气道炎症和重塑,还参与调节了屋尘螨(HDM)诱导的BEAS-2B细胞炎症反应。它减轻了支气管上皮细胞的炎症损伤,降低了氧化应激、细胞凋亡和线粒体膜电位丧失。机制上,我们观察到circ-0001454部分减轻了miR-770-5p过表达引起的上皮细胞炎症损伤、过量活性氧(ROS)产生、细胞凋亡和线粒体膜电位破坏。最后,我们发现circ-0001454靶向miR-770-5p并参与调节cbl-b的表达,进而调节表皮生长因子受体(EGFR)、蛋白激酶B(AKT1)和丝裂原活化蛋白激酶1(MAPK1)蛋白水平,从而减轻气道上皮细胞炎症。这些发现揭示了miR-770-5p在哮喘中的作用,以及circ-0001454如何通过与miR-770-5p结合并靶向cbl-b基因,有助于减轻气道炎症、降低ROS水平、抑制细胞凋亡和恢复线粒体膜电位。对cbl-b、EGFR、AKT1和MAPK1的这种调节提示了哮喘治疗的新潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a0/12011828/4e9fea23f328/fcell-13-1566223-g001.jpg

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