SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery

利用SARS-CoV-2感染原代人肺上皮细胞构建COVID-19模型和药物研发

阅读:5
作者:Apoorva Mulay ,Bindu Konda ,Gustavo Garcia Jr ,Changfu Yao ,Stephen Beil ,Jaquelyn M Villalba ,Colin Koziol ,Chandani Sen ,Arunima Purkayastha ,Jay K Kolls ,Derek A Pociask ,Patrizia Pessina ,Julio Sainz de Aja ,Carolina Garcia-de-Alba ,Carla F Kim ,Brigitte Gomperts ,Vaithilingaraja Arumugaswami ,Barry R Stripp

Abstract

Coronavirus disease 2019 (COVID-19) is the latest respiratory pandemic caused by severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2). Although infection initiates in the proximal airways, severe and sometimes fatal symptoms of the disease are caused by infection of the alveolar type 2 (AT2) cells of the distal lung and associated inflammation. In this study, we develop primary human lung epithelial infection models to understand initial responses of proximal and distal lung epithelium to SARS-CoV-2 infection. Differentiated air-liquid interface (ALI) cultures of proximal airway epithelium and alveosphere cultures of distal lung AT2 cells are readily infected by SARS-CoV-2, leading to an epithelial cell-autonomous proinflammatory response with increased expression of interferon signaling genes. Studies to validate the efficacy of selected candidate COVID-19 drugs confirm that remdesivir strongly suppresses viral infection/replication. We provide a relevant platform for study of COVID-19 pathobiology and for rapid drug screening against SARS-CoV-2 and emergent respiratory pathogens.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。