Three-Dimensional Human Alveolar Stem Cell Culture Models Reveal Infection Response to SARS-CoV-2

被引:157
|
作者
Youk, Jeonghwan [1 ,2 ]
Kim, Taewoo [1 ]
Evans, Kelly, V [3 ,4 ]
Jeong, Young-Il [5 ]
Hur, Yongsuk [6 ]
Hong, Seon Pyo [7 ]
Kim, Je Hyoung [5 ]
Yi, Kijong [1 ]
Kim, Su Yeon [1 ]
Na, Kwon Joong [8 ]
Bleazard, Thomas [9 ]
Kim, Ho Min [1 ,10 ]
Fellows, Mick [11 ]
Mahbubani, Krishnaa T. [12 ,13 ]
Saeb-Parsy, Kourosh [12 ,13 ]
Kim, Seon Young [14 ]
Kim, Young Tae [8 ]
Koh, Gou Young [7 ]
Choi, Byeong-Sun [5 ]
Ju, Young Seok [1 ,2 ]
Lee, Joo-Hyeon [3 ,4 ]
机构
[1] Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Daejeon 34141, South Korea
[2] GENOME INSIGHT Inc, Daejeon 34051, South Korea
[3] Univ Cambridge, Jeffrey Cheah Biomed Ctr, Wellcome MRC Cambridge Stem Cell Inst, Cambridge CB2 A0W, England
[4] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3EL, England
[5] Korea Ctr Dis Control & Prevent, Korea Natl Inst Hlth, Ctr Infect Dis Res, Div Viral Dis Res, Cheongju 28159, South Korea
[6] Korea Adv Inst Sci & Technol, BioMed Res Ctr, Daejeon 34141, South Korea
[7] Inst for Basic Sci Korea, Ctr Vasc Res, Daejeon 34126, South Korea
[8] Seoul Natl Univ, Seoul Natl Univ Hosp, Canc Res Inst, Dept Thorac & Cardiovasc Surg, Seoul 03080, South Korea
[9] Natl Inst Biol Stand & Controls, Blanche Lane, Potters Bar EN6 3QG, Herts, England
[10] Inst for Basic Sci Korea, Ctr Biomol & Cellular Struct, Daejeon 34126, South Korea
[11] AstraZeneca, R&D, Clin Pharmacol & Safety Sci, Cambridge, England
[12] Univ Cambridge, Dept Surg, Biomed Campus, Cambridge CB2 2QQ, England
[13] Univ Cambridge, Cambridge NIHR Biomed Res Ctr, Biomed Campus, Cambridge CB2 2QQ, England
[14] Chungnam Natl Univ, Coll Med, Dept Lab Med, Daejeon 35015, South Korea
基金
英国生物技术与生命科学研究理事会; 欧洲研究理事会; 新加坡国家研究基金会; 英国惠康基金;
关键词
RNA-SEQ DATA; SELF-RENEWAL; CORONAVIRUS; ORGANOIDS; POLARITY; ACE2; DIFFERENTIATION; QUANTIFICATION; PATTERNS; RECEPTOR;
D O I
10.1016/j.stem.2020.10.004
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is the cause of a present pandemic, infects human lung alveolar type 2 (hAT2) cells. Characterizing pathogenesis is crucial for developing vaccines and therapeutics. However. the lack of models mirroring the cellular physiology and pathology of hAT2 cells limits the study. Here, we develop a feeder-free, long-term, three-dimensional (3D) culture technique for hAT2 cells derived from primary human lung tissue and investigate infection response to SARS-CoV-2. By imaging-based analysis and single-cell transcriptome profiling, we reveal rapid viral replication and the increased expression of interferon-associated genes and proinflammatory genes in infected hAT2 cells, indicating a robust endogenous innate immune response. Further tracing of viral mutations acquired during transmission identifies full infection of individual cells effectively from a single viral entry. Our study provides deep insights into the pathogenesis of SARS-CoV-2 and the application of defined 3D hAT2 cultures as models for respiratory diseases.
引用
收藏
页码:905 / +
页数:25
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