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DOI 10.1038/s42003-022-03499-2

Медицинская библиотека · Communications biology · 2022

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

Sano Emi, Suzuki Tatsuya, Hashimoto Rina, Itoh Yumi, Sakamoto Ayaka, Sakai Yusuke, Saito Akatsuki, Okuzaki Daisuke, Motooka Daisuke, Muramoto Yukiko, Noda Takeshi, Takasaki Tomohiko, Sakuragi Jun-Ichi, Minami Shohei, Kobayashi Takeshi, Yamamoto Takuya, Matsumura Yasufumi, Nagao Miki, Okamoto Toru, Takayama Kazuo

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Аннотация

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.

Для цитирования: Sano Emi, Suzuki Tatsuya, Hashimoto Rina, Itoh Yumi, Sakamoto Ayaka, Sakai Yusuke, Saito Akatsuki, Okuzaki Daisuke, Motooka Daisuke, Muramoto Yukiko, Noda Takeshi, Takasaki Tomohiko, Sakuragi Jun-Ichi, Minami Shohei, Kobayashi Takeshi, Yamamoto Takuya, Matsumura Yasufumi, Nagao Miki, Okamoto Toru, Takayama Kazuo. Cell response analysis in SARS-CoV-2 infected bronchial organoids.. Communications biology. 2022. DOI: 10.1038/s42003-022-03499-2.

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