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Significant expression of FURIN and ACE2 on oral epithelial cells may facilitate the efficiency of SARS-CoV-2 entry
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covidontheweb.inria.fr
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Academic Article
research paper
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Significant expression of FURIN and ACE2 on oral epithelial cells may facilitate the efficiency of SARS-CoV-2 entry
Creator
Liu, Chang
Chen, Jian-Ming
Gao, Hong-Bin
Huang, Jiang-Yong
Lee, Learn-Han
Lin, Bing-Peng
Lin-Hu Ge,
Liu, Ming-Xiao
Qi, Cui-Ling
Wang, Li-Jing
Wang, Xin-Hong
Wu, Kai-Bin
Young, Andrew
Zhong, Mei
Source
BioRxiv
abstract
Background Leading to a sustained epidemic spread with >2,000,000 confirmed human infections, including >100,000 deaths, COVID-19 was caused by SARS-CoV-2 and resulted in acute respiratory distress syndrome (ARDS) and sepsis, which brought more challenges to the patient’s treatment. The S-glycoprotein, which recognized as the key factor for the entry of SARS-CoV-2 into the cell, contains two functional domains: an ACE2 receptor binding domain and a second domain necessary for fusion of the coronavirus and cell membranes. FURIN activity, exposes the binding and fusion domains, is essential for the zoonotic transmission of SARS-CoV-2. Moreover, it has been reported that ACE2 is likely to be the receptor for SARS-CoV-2. In addition, FURIN enzyme and ACE2 receptor were expressed in airway epithelia, cardiac tissue, and enteric canals, which considered as the potential target organ of the virus. However, report about the expression of FURIN and ACE2 in oral tissues was limited. Methods In order to investigate the potential infective channel of new coronavirus in oral cavity, we analyze the expression of ACE2 and FURIN that mediate the new coronavirus entry into host cells in oral mucosa using the public single-cell sequence datasets. Furthermore, immunohistochemical staining experiment was performed to confirm the expression of ACE2 and FURIN in the protein level. Results The bioinformatics results indicated the differential expression of ACE2 and FURIN on epithelial cells of different oral mucosal tissues and the proportion of FURIN-positive cells was obviously higher than that of ACE2-positive cells. IHC experiments revealed that both the ACE2-positive and FURIN-positive cells in the target tissues were mainly positioned in the epithelial layers, partly expressed in fibroblasts, which further confirm the bioinformatics results. Conclusions Based on these findings, we speculated that SARS-CoV-2 could effectively invade oral mucosal cells though two possible routes: binding to the ACE2 receptor and fusion with cell membrane activated by FURIN protease. Our results indicated that oral mucosa tissues are susceptible to SARS-CoV-2, which provides valuable information for virus-prevention strategy in clinical care as well as daily life.
has issue date
2020-04-22
(
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)
bibo:doi
10.1101/2020.04.18.047951
has license
biorxiv
sha1sum (hex)
ed532cfdb251b5bb5c2e121ce67f438d82616c8e
schema:url
https://doi.org/10.1101/2020.04.18.047951
resource representing a document's title
Significant expression of FURIN and ACE2 on oral epithelial cells may facilitate the efficiency of SARS-CoV-2 entry
schema:publication
bioRxiv
resource representing a document's body
covid:ed532cfdb251b5bb5c2e121ce67f438d82616c8e#body_text
is
schema:about
of
named entity 'SARS-CoV-2'
named entity 'cell'
named entity 'activity'
named entity 'tissue'
named entity 'ACE2'
named entity 'CARDIAC TISSUE'
named entity 'HUMAN'
named entity 'CELL MEMBRANES'
named entity 'ZOONOTIC'
named entity 'INFECTIONS'
named entity 'SUSTAINED'
named entity 'CAUSED BY'
named entity 'CONSIDERED'
named entity 'COVID-19'
named entity 'ACUTE RESPIRATORY DISTRESS SYNDROME'
named entity 'INCLUDING'
named entity '27S'
named entity 'FACTOR'
named entity 'CORONAVIRUS'
named entity 'SARS-COV-2'
covid:arg/ed532cfdb251b5bb5c2e121ce67f438d82616c8e
named entity 'SARS-CoV-2'
named entity 'enzyme'
named entity 'binding'
named entity 'infections'
named entity 'patient'
named entity 'ACE2'
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named entity 'airway epithelia'
named entity 'coronavirus'
named entity 'cell membranes'
named entity 'SARS-CoV-2'
named entity 'SARS-CoV-2'
named entity 'ACE2'
named entity 'ACE2'
named entity 'lip'
named entity 'gene'
named entity 'scRNA-seq'
named entity 'COVID'
named entity 'oral cavity'
named entity 'gingival'
named entity 'FURIN'
named entity 'cell types'
named entity 'epithelia'
named entity 'gingival tissues'
named entity 'ACE2'
named entity 'SARS-CoV-2'
named entity 'SARS-CoV-2'
named entity 'epithelial cells'
named entity 'FURIN'
named entity 'protein'
named entity 'human body'
named entity 'RNA sequencing'
named entity 'ACE2'
named entity 'ACE2'
named entity 'single-cell sequencing'
named entity 'pneumonia'
named entity 'Wuhan'
named entity 'one-way ANOVA'
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named entity 'epithelial cells'
named entity 'FURIN'
named entity 'personalized medicine'
named entity 'infection'
named entity 'spinous layer'
named entity 'coronavirus'
named entity 'public health'
named entity 'ACE2'
named entity 'clinical symptoms'
named entity 'fibroblasts'
named entity 'deep sequencing'
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