呼吸上皮
细胞因子
免疫学
炎症
上皮
粘液纤毛清除率
病理
内皮
肺
医学
生物
内科学
作者
Kambez H. Benam,Rémi Villenave,Carolina Lucchesi,Antonio Varone,Cédric Hubeau,Hyun‐Hee Lee,Stephen E. Alves,M Salmon,Thomas C. Ferrante,James C. Weaver,Anthony Bahinski,Geraldine A. Hamilton,Donald E. Ingber
出处
期刊:Nature Methods
[Springer Nature]
日期:2015-12-21
卷期号:13 (2): 151-157
被引量:676
摘要
The small airway-on-a-chip allows the recapitulation of human lung pathophysiology in vitro and analysis of responses to drugs. Here we describe the development of a human lung 'small airway-on-a-chip' containing a differentiated, mucociliary bronchiolar epithelium and an underlying microvascular endothelium that experiences fluid flow, which allows for analysis of organ-level lung pathophysiology in vitro. Exposure of the epithelium to interleukin-13 (IL-13) reconstituted the goblet cell hyperplasia, cytokine hypersecretion and decreased ciliary function of asthmatics. Small airway chips lined with epithelial cells from individuals with chronic obstructive pulmonary disease recapitulated features of the disease such as selective cytokine hypersecretion, increased neutrophil recruitment and clinical exacerbation by exposure to viral and bacterial infections. With this robust in vitro method for modeling human lung inflammatory disorders, it is possible to detect synergistic effects of lung endothelium and epithelium on cytokine secretion, identify new biomarkers of disease exacerbation and measure responses to anti-inflammatory compounds that inhibit cytokine-induced recruitment of circulating neutrophils under flow.
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