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Lysozyme Protects Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Inflammation in Human Corneal Epithelial Cells

PURPOSE: The purpose of this study was to investigate the effects of lysozyme, an antimicrobial enzyme found in tears that protects the eye against pathogens, on pseudotyped severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection through corneal epithelial cells. METHODS: The expressi...

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Autores principales: Song, Yinting, Zhang, Haokun, Zhu, Yanfang, Zhao, Xiao, Lei, Yi, Zhou, Wei, Yu, Jinguo, Dong, Xue, Wang, Xiaohong, Du, Mei, Yan, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206495/
https://www.ncbi.nlm.nih.gov/pubmed/35713893
http://dx.doi.org/10.1167/iovs.63.6.16
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author Song, Yinting
Zhang, Haokun
Zhu, Yanfang
Zhao, Xiao
Lei, Yi
Zhou, Wei
Yu, Jinguo
Dong, Xue
Wang, Xiaohong
Du, Mei
Yan, Hua
author_facet Song, Yinting
Zhang, Haokun
Zhu, Yanfang
Zhao, Xiao
Lei, Yi
Zhou, Wei
Yu, Jinguo
Dong, Xue
Wang, Xiaohong
Du, Mei
Yan, Hua
author_sort Song, Yinting
collection PubMed
description PURPOSE: The purpose of this study was to investigate the effects of lysozyme, an antimicrobial enzyme found in tears that protects the eye against pathogens, on pseudotyped severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection through corneal epithelial cells. METHODS: The expression of the angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease (TMPRSS2) in human corneal epithelial cells (HCECs) was measured by RT-PCR and Western blotting. The altered expression of the pro-inflammatory molecules induced by spike protein and lysozyme was analyzed by RT-PCR. Cell toxicity was tested by CCK8 assay. The cell entry of SAR-CoV-2 in HCECs and primary rabbit corneal epithelial cells (RbCECs) was detected by luciferase assay. RESULTS: ACE2 and TMPRSS2 were highly expressed in HCECs. The spike proteins of SARS-CoV-2 stimulated a robust inflammatory response in HCECs, characterized by increased secretion of pro-inflammatory molecules, including IL-6, TNF-α, iNOS, and MCP-1, and pretreatment with lysozyme in HCECs markedly decreased the production of proinflammatory molecules induced by spike proteins. In addition, the inflammatory cytokine TNF-α enhanced the entry of SARS-CoV-2 into HCECs, which can be mitigated by pretreatment with lysozyme. CONCLUSIONS: In this study, we analyzed the susceptibility of human corneal epithelial cells to SARS-CoV-2 infection and suggested the protective effects of lysozyme on SARS-CoV-2 infection.
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spelling pubmed-92064952022-06-19 Lysozyme Protects Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Inflammation in Human Corneal Epithelial Cells Song, Yinting Zhang, Haokun Zhu, Yanfang Zhao, Xiao Lei, Yi Zhou, Wei Yu, Jinguo Dong, Xue Wang, Xiaohong Du, Mei Yan, Hua Invest Ophthalmol Vis Sci Cornea PURPOSE: The purpose of this study was to investigate the effects of lysozyme, an antimicrobial enzyme found in tears that protects the eye against pathogens, on pseudotyped severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection through corneal epithelial cells. METHODS: The expression of the angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease (TMPRSS2) in human corneal epithelial cells (HCECs) was measured by RT-PCR and Western blotting. The altered expression of the pro-inflammatory molecules induced by spike protein and lysozyme was analyzed by RT-PCR. Cell toxicity was tested by CCK8 assay. The cell entry of SAR-CoV-2 in HCECs and primary rabbit corneal epithelial cells (RbCECs) was detected by luciferase assay. RESULTS: ACE2 and TMPRSS2 were highly expressed in HCECs. The spike proteins of SARS-CoV-2 stimulated a robust inflammatory response in HCECs, characterized by increased secretion of pro-inflammatory molecules, including IL-6, TNF-α, iNOS, and MCP-1, and pretreatment with lysozyme in HCECs markedly decreased the production of proinflammatory molecules induced by spike proteins. In addition, the inflammatory cytokine TNF-α enhanced the entry of SARS-CoV-2 into HCECs, which can be mitigated by pretreatment with lysozyme. CONCLUSIONS: In this study, we analyzed the susceptibility of human corneal epithelial cells to SARS-CoV-2 infection and suggested the protective effects of lysozyme on SARS-CoV-2 infection. The Association for Research in Vision and Ophthalmology 2022-06-17 /pmc/articles/PMC9206495/ /pubmed/35713893 http://dx.doi.org/10.1167/iovs.63.6.16 Text en Copyright 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Cornea
Song, Yinting
Zhang, Haokun
Zhu, Yanfang
Zhao, Xiao
Lei, Yi
Zhou, Wei
Yu, Jinguo
Dong, Xue
Wang, Xiaohong
Du, Mei
Yan, Hua
Lysozyme Protects Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Inflammation in Human Corneal Epithelial Cells
title Lysozyme Protects Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Inflammation in Human Corneal Epithelial Cells
title_full Lysozyme Protects Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Inflammation in Human Corneal Epithelial Cells
title_fullStr Lysozyme Protects Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Inflammation in Human Corneal Epithelial Cells
title_full_unstemmed Lysozyme Protects Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Inflammation in Human Corneal Epithelial Cells
title_short Lysozyme Protects Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Inflammation in Human Corneal Epithelial Cells
title_sort lysozyme protects against severe acute respiratory syndrome coronavirus 2 infection and inflammation in human corneal epithelial cells
topic Cornea
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206495/
https://www.ncbi.nlm.nih.gov/pubmed/35713893
http://dx.doi.org/10.1167/iovs.63.6.16
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