作者
Kristine M Abo, Liang Ma, Taylor Matte, Jessie Huang, Konstantinos D Alysandratos, Rhiannon B Werder, Aditya Mithal, Mary Lou Beermann, Jonathan Lindstrom-Vautrin, Gustavo Mostoslavsky, Laertis Ikonomou, Darrell N Kotton, Finn Hawkins, Andrew Wilson, Carlos Villacorta-Martin
发表日期
2020/6/4
期刊
Biorxiv
出版商
Cold Spring Harbor Laboratory Preprints
简介
Development of an anti-SARS-CoV-2 therapeutic is hindered by the lack of physiologically relevant model systems that can recapitulate host-viral interactions in human cell types, specifically the epithelium of the lung. Here, we compare induced pluripotent stem cell (iPSC)-derived alveolar and airway epithelial cells to primary lung epithelial cell controls, focusing on expression levels of genes relevant for COVID-19 disease modeling. iPSC-derived alveolar epithelial type II-like cells (iAT2s) and iPSC-derived airway epithelial lineages express key transcripts associated with lung identity in the majority of cells produced in culture. They express ACE2 and TMPRSS2, transcripts encoding essential host factors required for SARS-CoV-2 infection, in a minor subset of each cell sub-lineage, similar to frequencies observed in primary cells. In order to prepare human culture systems that are amenable to modeling viral …
引用总数
2020202120222023202442416113