Viroscience Department, Erasmus University Medical Center, Rotterdam, The Netherlands.
Oncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center, Utrecht, The Netherlands.
EMBO J. 2021 Mar 1;40(5):e105912. doi: 10.15252/embj.2020105912. Epub 2021 Jan 11.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19), which may result in acute respiratory distress syndrome (ARDS), multiorgan failure, and death. The alveolar epithelium is a major target of the virus, but representative models to study virus host interactions in more detail are currently lacking. Here, we describe a human 2D air-liquid interface culture system which was characterized by confocal and electron microscopy and single-cell mRNA expression analysis. In this model, alveolar cells, but also basal cells and rare neuroendocrine cells, are grown from 3D self-renewing fetal lung bud tip organoids. These cultures were readily infected by SARS-CoV-2 with mainly surfactant protein C-positive alveolar type II-like cells being targeted. Consequently, significant viral titers were detected and mRNA expression analysis revealed induction of type I/III interferon response program. Treatment of these cultures with a low dose of interferon lambda 1 reduced viral replication. Hence, these cultures represent an experimental model for SARS-CoV-2 infection and can be applied for drug screens.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)可引起 2019 年冠状病毒病(COVID-19),可能导致急性呼吸窘迫综合征(ARDS)、多器官衰竭和死亡。肺泡上皮是该病毒的主要靶标,但目前缺乏用于更详细研究病毒宿主相互作用的代表性模型。在这里,我们描述了一种人 2D 气液界面培养系统,该系统通过共聚焦和电子显微镜以及单细胞 mRNA 表达分析进行了表征。在该模型中,肺泡细胞、基底细胞和罕见的神经内分泌细胞均来自 3D 自我更新的胎儿肺芽尖端类器官生长。这些培养物容易被 SARS-CoV-2 感染,主要靶向表面活性剂蛋白 C 阳性的肺泡 II 型样细胞。因此,检测到显著的病毒滴度,mRNA 表达分析显示诱导了 I/III 型干扰素反应程序。用低剂量干扰素 lambda 1 处理这些培养物可减少病毒复制。因此,这些培养物代表了 SARS-CoV-2 感染的实验模型,可用于药物筛选。