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微小 RNA-375 通过柴油机排气颗粒和环境颗粒物对人支气管上皮细胞中胸腺基质淋巴细胞生成素的调控作用。

MicroRNA-375 regulation of thymic stromal lymphopoietin by diesel exhaust particles and ambient particulate matter in human bronchial epithelial cells.

机构信息

Department of Medicine, New York University School of Medicine, New York, NY 10016, USA.

出版信息

J Immunol. 2013 Apr 1;190(7):3757-63. doi: 10.4049/jimmunol.1201165. Epub 2013 Mar 1.

DOI:10.4049/jimmunol.1201165
PMID:23455502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3665109/
Abstract

Air pollution contributes to acute exacerbations of asthma and the development of asthma in children and adults. Airway epithelial cells interface innate and adaptive immune responses, and have been proposed to regulate much of the response to pollutants. Thymic stromal lymphopoietin (TSLP) is a pivotal cytokine linking innate and Th2 adaptive immune disorders, and is upregulated by environmental pollutants, including ambient particulate matter (PM) and diesel exhaust particles (DEP). We show that DEP and ambient fine PM upregulate TSLP mRNA and human microRNA (hsa-miR)-375 in primary human bronchial epithelial cells (pHBEC). Moreover, transfection of pHBEC with anti-hsa-miR-375 reduced TSLP mRNA in DEP but not TNF-α-treated cells. In silico pathway evaluation suggested the aryl hydrocarbon receptor (AhR) as one possible target of miR-375. DEP and ambient fine PM (3 μg/cm(2)) downregulated AhR mRNA. Transfection of mimic-hsa-miR-375 resulted in a small downregulation of AhR mRNA compared with resting AhR mRNA. AhR mRNA was increased in pHBEC treated with DEP after transfection with anti-hsa-miR-375. Our data show that two pollutants, DEP and ambient PM, upregulate TSLP in human bronchial epithelial cells by a mechanism that includes hsa-miR-375 with complex regulatory effects on AhR mRNA. The absence of this pathway in TNF-α-treated cells suggests multiple regulatory pathways for TSLP expression in these cells.

摘要

空气污染可导致哮喘急性加重以及儿童和成人哮喘的发生。气道上皮细胞可影响固有免疫和适应性免疫应答,且被认为可调控机体对污染物的大部分应答。胸腺基质淋巴细胞生成素(TSLP)是连接固有免疫和 Th2 适应性免疫紊乱的关键细胞因子,可被环境污染物(包括环境细颗粒物(PM)和柴油废气颗粒(DEP))上调。我们发现 DEP 和环境细 PM 可上调原代人支气管上皮细胞(pHBEC)中的 TSLP mRNA 和人 microRNA(hsa-miR)-375。此外,用抗 hsa-miR-375 转染 pHBEC 可降低 DEP 但不降低 TNF-α处理的细胞中的 TSLP mRNA。计算机通路分析提示芳烃受体(AhR)可能是 miR-375 的一个靶标。DEP 和环境细 PM(3μg/cm2)可下调 AhR mRNA。与静息 AhR mRNA 相比,转染 mimics-hsa-miR-375 可导致 AhR mRNA 轻度下调。用 DEP 转染 pHBEC 后,再用抗 hsa-miR-375 转染,可增加 AhR mRNA。我们的数据表明,两种污染物,DEP 和环境 PM,通过包括 hsa-miR-375 在内的机制上调人支气管上皮细胞中的 TSLP,该机制对 AhR mRNA 具有复杂的调控作用。TNF-α处理的细胞中不存在该通路,提示这些细胞中 TSLP 表达存在多种调控通路。

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