Cargando…
Up-regulation of IL-6 and TNF-α induced by SARS-coronavirus spike protein in murine macrophages via NF-κB pathway
The clinical picture of severe acute respiratory syndrome (SARS) is characterized by an over-exuberant immune response with lung lymphomononuclear cells infilteration and proliferation that may account for tissue damage more than the direct effect of viral replication. To understand how cells respon...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114322/ https://www.ncbi.nlm.nih.gov/pubmed/17532082 http://dx.doi.org/10.1016/j.virusres.2007.02.007 |
_version_ | 1783513860990304256 |
---|---|
author | Wang, Wei Ye, Linbai Ye, Li Li, Baozong Gao, Bo Zeng, Yingchun Kong, Lingbao Fang, Xiaonan Zheng, Hong Wu, Zhenghui She, Yinglong |
author_facet | Wang, Wei Ye, Linbai Ye, Li Li, Baozong Gao, Bo Zeng, Yingchun Kong, Lingbao Fang, Xiaonan Zheng, Hong Wu, Zhenghui She, Yinglong |
author_sort | Wang, Wei |
collection | PubMed |
description | The clinical picture of severe acute respiratory syndrome (SARS) is characterized by an over-exuberant immune response with lung lymphomononuclear cells infilteration and proliferation that may account for tissue damage more than the direct effect of viral replication. To understand how cells response in the early stage of virus–host cell interaction, in this study, a purified recombinant S protein was studied for stimulating murine macrophages (RAW264.7) to produce proinflammatory cytokines (IL-6 and TNF-α) and chemokine IL-8. We found that direct induction of IL-6 and TNF-α release in the supernatant in a dose-, time-dependent manner and highly spike protein-specific, but no induction of IL-8 was detected. Further experiments showed that IL-6 and TNF-α production were dependent on NF-κB, which was activated through I-κBα degradation. These results suggest that SARS-CoV spike protein may play an important role in the pathogenesis of SARS, especially in inflammation and high fever. |
format | Online Article Text |
id | pubmed-7114322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71143222020-04-02 Up-regulation of IL-6 and TNF-α induced by SARS-coronavirus spike protein in murine macrophages via NF-κB pathway Wang, Wei Ye, Linbai Ye, Li Li, Baozong Gao, Bo Zeng, Yingchun Kong, Lingbao Fang, Xiaonan Zheng, Hong Wu, Zhenghui She, Yinglong Virus Res Article The clinical picture of severe acute respiratory syndrome (SARS) is characterized by an over-exuberant immune response with lung lymphomononuclear cells infilteration and proliferation that may account for tissue damage more than the direct effect of viral replication. To understand how cells response in the early stage of virus–host cell interaction, in this study, a purified recombinant S protein was studied for stimulating murine macrophages (RAW264.7) to produce proinflammatory cytokines (IL-6 and TNF-α) and chemokine IL-8. We found that direct induction of IL-6 and TNF-α release in the supernatant in a dose-, time-dependent manner and highly spike protein-specific, but no induction of IL-8 was detected. Further experiments showed that IL-6 and TNF-α production were dependent on NF-κB, which was activated through I-κBα degradation. These results suggest that SARS-CoV spike protein may play an important role in the pathogenesis of SARS, especially in inflammation and high fever. Published by Elsevier B.V. 2007-09 2007-05-25 /pmc/articles/PMC7114322/ /pubmed/17532082 http://dx.doi.org/10.1016/j.virusres.2007.02.007 Text en Copyright © 2007 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Wang, Wei Ye, Linbai Ye, Li Li, Baozong Gao, Bo Zeng, Yingchun Kong, Lingbao Fang, Xiaonan Zheng, Hong Wu, Zhenghui She, Yinglong Up-regulation of IL-6 and TNF-α induced by SARS-coronavirus spike protein in murine macrophages via NF-κB pathway |
title | Up-regulation of IL-6 and TNF-α induced by SARS-coronavirus spike protein in murine macrophages via NF-κB pathway |
title_full | Up-regulation of IL-6 and TNF-α induced by SARS-coronavirus spike protein in murine macrophages via NF-κB pathway |
title_fullStr | Up-regulation of IL-6 and TNF-α induced by SARS-coronavirus spike protein in murine macrophages via NF-κB pathway |
title_full_unstemmed | Up-regulation of IL-6 and TNF-α induced by SARS-coronavirus spike protein in murine macrophages via NF-κB pathway |
title_short | Up-regulation of IL-6 and TNF-α induced by SARS-coronavirus spike protein in murine macrophages via NF-κB pathway |
title_sort | up-regulation of il-6 and tnf-α induced by sars-coronavirus spike protein in murine macrophages via nf-κb pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114322/ https://www.ncbi.nlm.nih.gov/pubmed/17532082 http://dx.doi.org/10.1016/j.virusres.2007.02.007 |
work_keys_str_mv | AT wangwei upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT yelinbai upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT yeli upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT libaozong upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT gaobo upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT zengyingchun upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT konglingbao upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT fangxiaonan upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT zhenghong upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT wuzhenghui upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway AT sheyinglong upregulationofil6andtnfainducedbysarscoronavirusspikeproteininmurinemacrophagesvianfkbpathway |