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SARS-CoV-2 感染的支气管类器官中的细胞反应分析。

Cell response analysis in SARS-CoV-2 infected bronchial organoids.

机构信息

Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan.

Institute for Advanced Co-Creation Studies, Research Institute for Microbial Diseases, Osaka University, Suita, 565-0871, Japan.

出版信息

Commun Biol. 2022 May 30;5(1):516. doi: 10.1038/s42003-022-03499-2.

Abstract

The development of an in vitro cell model that can be used to study severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) research is expected. Here we conducted infection experiments in bronchial organoids (BO) and an BO-derived air-liquid interface model (BO-ALI) using 8 SARS-CoV-2 variants. The infection efficiency in BO-ALI was more than 1,000 times higher than that in BO. Among the bronchial epithelial cells, we found that ciliated cells were infected with the virus, but basal cells were not. Ciliated cells died 7 days after the viral infection, but basal cells survived after the viral infection and differentiated into ciliated cells. Fibroblast growth factor 10 signaling was essential for this differentiation. These results indicate that BO and BO-ALI may be used not only to evaluate the cell response to SARS-CoV-2 and coronavirus disease 2019 (COVID-19) therapeutic agents, but also for airway regeneration studies.

摘要

预计将开发一种能够用于研究严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 的体外细胞模型。在这里,我们使用 8 种 SARS-CoV-2 变体在支气管类器官 (BO) 和 BO 衍生的气液界面模型 (BO-ALI) 中进行了感染实验。BO-ALI 中的感染效率比 BO 高 1000 多倍。在支气管上皮细胞中,我们发现纤毛细胞被病毒感染,但基底细胞没有。纤毛细胞在病毒感染后 7 天死亡,但基底细胞在病毒感染后存活并分化为纤毛细胞。成纤维细胞生长因子 10 信号对于这种分化是必不可少的。这些结果表明,BO 和 BO-ALI 不仅可用于评估细胞对 SARS-CoV-2 和 2019 年冠状病毒病 (COVID-19) 治疗剂的反应,还可用于气道再生研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a97d/9151746/0e1f277e9b69/42003_2022_3499_Fig1_HTML.jpg

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