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变应性哮喘患者的中性粒细胞在直接接触过敏原后会产生和释放基质金属蛋白酶-9。

Neutrophils from allergic asthmatic patients produce and release metalloproteinase-9 upon direct exposure to allergens.

机构信息

Servicio Regional de Inmunología y Alergia, Hospital Universitario Virgen Macarena, Sevilla, Spain.

出版信息

Allergy. 2014 Jul;69(7):898-905. doi: 10.1111/all.12414. Epub 2014 Apr 29.

Abstract

BACKGROUND

Asthma is characterized by airway inflammation and remodelling in which matrix metalloproteinases (MMPs) play an important role. MMP-9 is the major MMP found in the bronchoalveolar lavage fluids and bronchial biopsies from patients with allergic asthma after allergen challenge, where it correlates with the count of neutrophils and macrophages. However, the cellular sources of MMP-9 in this inflammatory condition have not yet been clearly identified. This work was undertaken to analyse whether neutrophils may be a source of MMP-9 in the allergic asthma condition upon allergen challenge.

METHODS

Neutrophils from allergic asthmatic patients were in vitro stimulated, and the levels of MMP-9 release were measured in the cell culture supernatants using enzyme-linked immunosorbent assay (ELISA) and zymography.

RESULTS

We show that MMP-9 is released by neutrophils, but not by eosinophils from allergic asthmatic patients in response to allergens to which the patients were sensitized. Neutrophils also released MMP-9 in response to anti-IgE Abs, and agonist Abs against FcεRI, FcεRII/CD23 and galectin-3. Inhibitors of transcription and translation, actinomycin D and cycloheximide, partially cancelled this process, suggesting that MMP-9 is also de novo synthesized in response to stimuli. We also show evidence that the MAPKs, p38 and extracellular signal-regulated kinase, as well as the transcription factor NF-κB, are involved, as specific chemical inhibitors of these cell-signalling pathways abolished the anti-IgE/allergen-dependent MMP-9 release.

CONCLUSIONS

These data demonstrate that the exposure of neutrophils to allergens leads to generation of MMP-9, which may then lead to remodelling in asthma.

摘要

背景

哮喘的特征是气道炎症和重塑,其中基质金属蛋白酶(MMPs)起着重要作用。MMP-9 是变应原刺激后过敏性哮喘患者支气管肺泡灌洗液和支气管活检中主要的 MMP,与中性粒细胞和巨噬细胞计数相关。然而,这种炎症状态下 MMP-9 的细胞来源尚未明确。本研究旨在分析变应原刺激后,中性粒细胞是否可能成为过敏性哮喘中 MMP-9 的来源。

方法

体外刺激过敏性哮喘患者的中性粒细胞,并用酶联免疫吸附试验(ELISA)和胶乳酶谱法测量细胞培养上清液中 MMP-9 的释放水平。

结果

我们表明,MMP-9 是由对致敏变应原产生反应的过敏性哮喘患者的中性粒细胞而不是嗜酸性粒细胞释放的。中性粒细胞也对抗 IgE Ab 和 FcεRI、FcεRII/CD23 和半乳糖凝集素-3 的激动性 Ab 释放 MMP-9。转录和翻译抑制剂,放线菌素 D 和环己酰亚胺,部分阻断了这一过程,表明 MMP-9 也是在刺激后新合成的。我们还提供了证据表明,MAPKs p38 和细胞外信号调节激酶以及转录因子 NF-κB 参与其中,因为这些细胞信号通路的特异性化学抑制剂消除了抗 IgE/变应原依赖性 MMP-9 释放。

结论

这些数据表明,中性粒细胞暴露于变应原会导致 MMP-9 的产生,这可能导致哮喘的重塑。

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