Summary of ssbd-repos-000291

SSBD:database
URL

Name
ssbd-repos-000291 (291-Deguchi-SARS-CoV2)
URL
DOI
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Title
Fluorescence images of immunostaining analysis of SARS-CoV-2 NP in hepatocytes of bile duct (ibd-LoC) or blood vessel (bv-LoC) at 2 or 6 days post-infection (dpi).
Description
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Submited Date
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Release Date
2023-07-20
Updated Date
-
License
Funding information
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File formats
Data size
5.9 MB

Organism
Homo sapiens
Strain
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Cell Line
hepatocyte
Genes
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Proteins
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GO Molecular Function (MF)
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GO Biological Process (BP)
viral gene expression, cellular response to virus
GO Cellular Component (CC)
nucleus
Study Type
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Imaging Methods
fluorescence microscopy

Method Summary
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Related paper(s)

Sayaka Deguchi, Kaori Kosugi, Rina Hashimoto, Ayaka Sakamoto, Masaki Yamamoto, Rafal P Krol, Peter Gee, Ryosuke Negoro, Takeshi Noda, Takuya Yamamoto, Yu-Suke Torisawa, Miki Nagao, Kazuo Takayama (2023) Elucidation of the liver pathophysiology of COVID-19 patients using liver-on-a-chips., PNAS nexus, Volume 2, Number 3, pp. pgad029

Published in 2023 Mar (Electronic publication in March 7, 2023, midnight )

(Abstract) SARS-CoV-2 induces severe organ damage not only in the lung but also in the liver, heart, kidney, and intestine. It is known that COVID-19 severity correlates with liver dysfunction, but few studies have investigated the liver pathophysiology in COVID-19 patients. Here, we elucidated liver pathophysiology in COVID-19 patients using organs-on-a-chip technology and clinical analyses. First, we developed liver-on-a-chip (LoC) which recapitulating hepatic functions around the intrahepatic bile duct and blood vessel. We found that hepatic dysfunctions, but not hepatobiliary diseases, were strongly induced by SARS-CoV-2 infection. Next, we evaluated the therapeutic effects of COVID-19 drugs to inhibit viral replication and recover hepatic dysfunctions, and found that the combination of anti-viral and immunosuppressive drugs (Remdesivir and Baricitinib) is effective to treat hepatic dysfunctions caused by SARS-CoV-2 infection. Finally, we analyzed the sera obtained from COVID-19 patients, and revealed that COVID-19 patients, who were positive for serum viral RNA, are likely to become severe and develop hepatic dysfunctions, as compared with COVID-19 patients who were negative for serum viral RNA. We succeeded in modeling the liver pathophysiology of COVID-19 patients using LoC technology and clinical samples.

Contact(s)
Kazuo Takayama
Organization(s)
Kyoto University , Center for iPS Cell Research and Application (CiRA)
Image Data Contributors
Quantitative Data Contributors

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