Hayman Yvette A, Sadofsky Laura R, Williamson James D, Hart Simon P, Morice Alyn H
Centre for Cardiovascular and Metabolic Research, Hull York Medical School, University of Hull, Hull , UK.
ERJ Open Res. 2017 Mar 20;3(1). doi: 10.1183/23120541.00026-2016. eCollection 2017 Jan.
Chronic inflammatory diseases of the airways are associated with gastro-oesophageal reflux (GOR) and aspiration events. The observation of lipid-laden macrophages (LLMs) within the airway may indicate aspiration secondary to GOR. The proposed mechanism, that lipid droplets from undigested or partially digested food are aspirated leading to accumulation in scavenging macrophages, led us to hypothesise that an activated population of LLMs could interact with other immune cells to induce bronchial inflammation. To test this, we generated an model using differentiated THP-1 cells, which were treated with a high-fat liquid feed. Here, we show that THP-1 cells can take up lipid from the high-fat feed independent of actin polymerisation or CD36-dependent phagocytosis. These cells did not exhibit M1 or M2 polarisation. Gene array analysis confirmed over 8000 genes were upregulated by at least twofold following high fat exposure, and IL-8 was the most upregulated gene. Pathway analysis revealed upregulation of genes known to be involved in chronic obstructive pulmonary disease (COPD) pathophysiology. We suggest that aspiration and macrophage phagocytosis may be important mechanisms in the aetiology of diseases such as COPD and cystic fibrosis that are characterised by high levels of IL-8 within the airways.
气道慢性炎症性疾病与胃食管反流(GOR)及误吸事件相关。气道内出现充满脂质的巨噬细胞(LLMs)可能提示继发于GOR的误吸。推测的机制是,未消化或部分消化食物中的脂滴被误吸,导致其在清除性巨噬细胞中蓄积,这使我们推测活化的LLMs群体可能与其他免疫细胞相互作用以诱导支气管炎症。为验证这一点,我们使用经分化的THP-1细胞构建了一个模型,并用高脂液体饲料对其进行处理。在此,我们表明THP-1细胞可从高脂饲料中摄取脂质,且与肌动蛋白聚合或CD36依赖性吞噬作用无关。这些细胞未表现出M1或M2极化。基因阵列分析证实,高脂暴露后超过8000个基因上调至少两倍,其中IL-8是上调最明显的基因。通路分析显示,已知参与慢性阻塞性肺疾病(COPD)病理生理学的基因上调。我们认为,误吸和巨噬细胞吞噬作用可能是COPD和囊性纤维化等疾病病因学中的重要机制,这些疾病的特征是气道内IL-8水平升高。