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细颗粒物通过细胞外囊泡包裹的 Let-7i-5p 介导的 MAPK 信号通路调控诱导儿童哮喘发作。

Fine Particulate Matter Induces Childhood Asthma Attacks via Extracellular Vesicle-Packaged Let-7i-5p-Mediated Modulation of the MAPK Signaling Pathway.

机构信息

Department of Genetic Toxicology, The Key Laboratory of Modern Toxicology of Ministry of Education, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, 211166, China.

Department of Environmental Genomics, Jiangsu Key Laboratory of Cancer Biomarkers, Prevention and Treatment, Collaborative Innovation Center for Cancer Personalized Medicine, Nanjing Medical University, Nanjing, 211166, China.

出版信息

Adv Sci (Weinh). 2022 Jan;9(3):e2102460. doi: 10.1002/advs.202102460. Epub 2021 Nov 23.

Abstract

Fine particulate matter less than 2.5 µm in diameter (PM ) is a major risk factor for acute asthma attacks in children. However, the biological mechanism underlying this association remains unclear. In the present study, PM -treated HBE cells-secreted extracellular vesicles (PM -EVs) caused cytotoxicity in "horizontal" HBE cells and increased the contractility of "longitudinal" sensitive human bronchial smooth muscle cells (HBSMCs). RNA sequencing showed that let-7i-5p is significantly overexpressed in PM -EVs and asthmatic plasma; additionally, its level is correlated with PM exposure in children with asthma. The combination of EV-packaged let-7i-5p and the traditional clinical biomarker IgE exhibits the best diagnostic performance (area under the curve [AUC] = 0.855, 95% CI = 0.786-0.923). Mechanistically, let-7i-5p is packaged into PM -EVs by interacting with ELAVL1 and internalized by both "horizontal" recipient HBE cells and "longitudinal" recipient-sensitive HBSMCs, with subsequent activation of the MAPK signaling pathway via suppression of its target DUSP1. Furthermore, an injection of EV-packaged let-7i-5p into PM -treated juvenile mice aggravated asthma symptoms. This comprehensive study deciphered the remodeling of the extracellular environment mediated by the secretion of let-7i-5p-enriched EVs during PM -induced asthma attacks and identified plasma EV-packaged let-7i-5p as a novel predictor of childhood asthma.

摘要

直径小于 2.5μm 的细颗粒物(PM )是儿童急性哮喘发作的主要危险因素。然而,这种关联的生物学机制尚不清楚。在本研究中,PM 处理的 HBE 细胞分泌的细胞外囊泡(PM-EVs)在“水平”HBE 细胞中引起细胞毒性,并增加“纵向”敏感人支气管平滑肌细胞(HBSMCs)的收缩性。RNA 测序显示,let-7i-5p 在 PM-EVs 和哮喘患者血浆中显著过表达;此外,其水平与儿童 PM 暴露相关。包含 EV 封装的 let-7i-5p 和传统临床生物标志物 IgE 的组合表现出最佳的诊断性能(曲线下面积 [AUC] = 0.855,95%CI = 0.786-0.923)。从机制上讲,let-7i-5p 通过与 ELAVL1 相互作用被包装到 PM-EVs 中,并被“水平”受体 HBE 细胞和“纵向”受体敏感 HBSMCs 内化,随后通过抑制其靶标 DUSP1 激活 MAPK 信号通路。此外,向 PM 处理的幼年小鼠注射 EV 封装的 let-7i-5p 加重了哮喘症状。这项全面的研究揭示了在 PM 诱导的哮喘发作期间,由富含 let-7i-5p 的 EV 分泌介导的细胞外环境重塑,并鉴定出血浆 EV 封装的 let-7i-5p 作为儿童哮喘的新型预测因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be0e/8787417/c46e54dd3d6d/ADVS-9-2102460-g002.jpg

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