呼吸上皮
病毒复制
感染的多重性
病毒学
生物
细胞病变效应
粘液
病毒
肺
气道
免疫学
上皮
医学
生态学
遗传学
外科
内科学
作者
Yunji Lee,Myoung Kyu Lee,Hwa‐Rim Lee,Byungil Kim,Meehyein Kim,Sungjune Jung
出处
期刊:Biomaterials
[Elsevier]
日期:2024-06-25
卷期号:311: 122689-122689
被引量:1
标识
DOI:10.1016/j.biomaterials.2024.122689
摘要
We present a bioprinted three-layered airway model with a physiologically relevant microstructure for the study of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection dynamics. This model exhibited clear cell-cell junctions and mucus secretion with an efficient expression of angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2). Having infected air-exposed epithelial cells in the upper layer with a minimum multiplicity of infection of 0.01, the airway model showed a marked susceptibility to SARS-CoV-2 within one-day post-infection (dpi). Furthermore, the unique longevity allowed the observation of cytopathic effects and barrier degradation for 21 dpi. The in-depth transcriptomic analysis revealed dramatic changes in gene expression affecting the infection pathway, viral proliferation, and host immune response which are consistent with COVID-19 patient data. Finally, the treatment of antiviral agents, such as remdesivir and molnupiravir, through the culture medium underlying the endothelium resulted in a marked inhibition of viral replication within the epithelium. The bioprinted airway model can be used as a manufacturable physiological platform to study disease pathogeneses and drug efficacy.
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