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About:
ACE2 expression by colonic epithelial cells is associated with viral infection, immunity and energy metabolism
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schema:ScholarlyArticle
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
ACE2 expression by colonic epithelial cells is associated with viral infection, immunity and energy metabolism
Creator
Zhang, Yan
Zhao, Jincun
Wang, Ping
Wang, Jun
Huang, Bing
Liu, Ming
Xu, Yanhui
Cui, Jun
Luo, Hai-Bin
Zhang, Yuxia
Bai, Fan
Chen, Zhanghua
Lew, Andrew
Lin, Meng
Zhao, Zhiyao
Xu, Yiping
Zhao, Shanmeizi
Zuo, Xiaoyu
Source
MedRxiv
abstract
Respiratory disease caused by the 2019 novel coronavirus (2019-nCoV) pneumonia first emerged in Wuhan, Hubei Province, China, in December 2019 and spread rapidly to other provinces and other countries. Angiotensin-converting enzyme 2 (ACE2) is the receptor for SARS-CoV and has been suggested to be also the receptor for 2019-nCoV. Paradoxically, ACE2 expression in the lung protects mice from SARS-CoV spike protein induced lung injury by attenuating the renin-angiotensin system. In the intestine, ACE2 also suppresses intestinal inflammation by maintaining amino acid homeostasis, antimicrobial peptide expression and ecology of the gut microbiome. Upon analysis of single cell-RNA sequencing data from control subjects and those with colitis or inflammatory bowel disease (IBD), we found that ACE2 expression in the colonocytes was positively associated with genes regulating viral infection, innate and cellular immunity, but was negatively associated with viral transcription, protein translation, humoral immunity, phagocytosis and complement activation. In summary, we suggest that ACE2 may play dual roles in mediating the susceptibility and immunity of 2019-nCoV infection.
has issue date
2020-02-07
(
xsd:dateTime
)
bibo:doi
10.1101/2020.02.05.20020545
has license
medrxiv
sha1sum (hex)
ce5e7eeb8df10f0e4fb08b0dc78730fd2630a90c
schema:url
https://doi.org/10.1101/2020.02.05.20020545
resource representing a document's title
ACE2 expression by colonic epithelial cells is associated with viral infection, immunity and energy metabolism
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covid:ce5e7eeb8df10f0e4fb08b0dc78730fd2630a90c#body_text
is
schema:about
of
named entity 'pneumonia'
named entity 'Angiotensin-converting enzyme 2'
named entity 'expression'
named entity 'pneumonia'
named entity '2019-nCoV'
named entity 'inflammatory bowel disease'
named entity 'control subjects'
named entity 'RAS'
named entity '2019-nCoV'
named entity 'cytotoxicity'
named entity 'lung'
named entity 'RNA sequencing'
named entity 'COPD'
named entity 'ACE2'
named entity 'Novartis'
named entity 'single-cell'
named entity 'ACE2'
named entity 'peer-reviewed'
named entity 'innate immunity'
named entity 'deep-vein thrombosis'
named entity 'ACE2'
named entity 'data normalization'
named entity 'United States'
named entity '10x genomics'
named entity 'demultiplex'
named entity 'single-cell'
named entity 'antimicrobial peptide'
named entity 'neprilysin inhibitor'
named entity 'SARS-CoV'
named entity 'Guangzhou'
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named entity 'medRxiv'
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named entity '2019-nCoV'
named entity 'lung fibrosis'
named entity 'bioinformatic analysis'
named entity 'spike protein'
named entity 'pulmonary embolism'
named entity 'inflammation'
named entity 'inflammation'
named entity 'homeostasis'
named entity 'RNA sequencing'
named entity 'viral entry'
named entity 'tSNE'
named entity 'lungs'
named entity 'sacubitril'
named entity 'antimicrobial peptide'
named entity 'humoral immunity'
named entity 'spike protein'
named entity 'intestine'
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named entity 'dimension reduction'
named entity 'Gene Ontology'
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named entity '10x Genomics'
named entity 'type II alveolar cells'
named entity 'ACE2'
named entity 'clinical outcomes'
named entity '2019-nCoV'
named entity 'control subjects'
named entity 'human intestine'
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