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MiR-493-5p inhibits Th9 cell differentiation in allergic asthma by targeting FOXO1

The role of micro RNAs (miRNAs) in asthma remains unclear. In this study, we examined the role of miRNA in targeting FOXO1 in asthma. Results showed that miR-493-5p was one of the differentially expressed miRNAs in the PBMCs of asthmatic children, and was also associated with Th cell differentiation...

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Detalles Bibliográficos
Autores principales: Rao, Xingyu, Dong, Heting, Zhang, Weili, Sun, Huiming, Gu, Wenjing, Zhang, Xinxing, Huang, Li, Yan, Yongdong, Hao, Chuangli, Ji, Wei, Zhu, Canhong, Chen, Zhengrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578235/
https://www.ncbi.nlm.nih.gov/pubmed/36253857
http://dx.doi.org/10.1186/s12931-022-02207-2
Descripción
Sumario:The role of micro RNAs (miRNAs) in asthma remains unclear. In this study, we examined the role of miRNA in targeting FOXO1 in asthma. Results showed that miR-493-5p was one of the differentially expressed miRNAs in the PBMCs of asthmatic children, and was also associated with Th cell differentiation. The miR-493-5p expression decreased significantly in the OVA-induced asthma mice than the control groups. The miR-493-5p mimic inhibited the expression of the IL-9, IRF4 and FOXO1, while the inhibitor restored these effects. Moreover, the Dual-Luciferase analysis results showed FOXO1 as a novel valid target of miR-493-5p. According to the rescue experiment, miR-493-5p inhibited Th9 cell differentiation by targeting FOXO1. Then the exosomes in association with the pathogenesis of asthma was identified. Various inflammatory cells implicated in asthmatic processes including B and T lymphocytes, DCs, mast cells, and epithelial cells can release exosomes. Our results demonstrated that the DC-derived exosomes can inhibit Th9 cell differentiation through miR-493-5p, thus DC-derived exosomal miR-493-5p/FOXO1/Th9 may serve as a potential therapeutic target in the development of asthma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-022-02207-2.