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Proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-A virus
Macrophages have a vital role in phagocytosis and antiviral effect against invading influenza viruses. Previously, we found that methionine enkephalin (MENK) inhibited influenza virus infection by upregulating the “antiviral state” of macrophages. To investigate the immunoregulatory mechanism of act...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088144/ https://www.ncbi.nlm.nih.gov/pubmed/37041527 http://dx.doi.org/10.1186/s12953-023-00205-w |
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author | Fu, Wenrui Xie, Zifeng Bai, Mei Zhang, Zhen Zhao, Yuanlong Tian, Jing |
author_facet | Fu, Wenrui Xie, Zifeng Bai, Mei Zhang, Zhen Zhao, Yuanlong Tian, Jing |
author_sort | Fu, Wenrui |
collection | PubMed |
description | Macrophages have a vital role in phagocytosis and antiviral effect against invading influenza viruses. Previously, we found that methionine enkephalin (MENK) inhibited influenza virus infection by upregulating the “antiviral state” of macrophages. To investigate the immunoregulatory mechanism of action of MENK on macrophages, we employed proteomic analysis to identify differentially expressed proteins (DEPs) between macrophages infected with the influenza-A virus and cells infected with the influenza-A virus after pretreatment with MENK. A total of 215 DEPs were identified: 164 proteins had upregulated expression and 51 proteins had downregulated expression. Proteomics analysis showed that DEPs were highly enriched in “cytokine-cytokine receptor interaction”, “phagosome”, and “complement and coagulation cascades pathway”. Proteomics analysis revealed that MENK could be an immune modulator or prophylactic for the prevention and treatment of influenza. MENK promoted the polarization of M1 macrophages, activated inflammatory responses, and enhanced phagocytosis and killing function by upregulating opsonizing receptors. |
format | Online Article Text |
id | pubmed-10088144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100881442023-04-12 Proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-A virus Fu, Wenrui Xie, Zifeng Bai, Mei Zhang, Zhen Zhao, Yuanlong Tian, Jing Proteome Sci Research Macrophages have a vital role in phagocytosis and antiviral effect against invading influenza viruses. Previously, we found that methionine enkephalin (MENK) inhibited influenza virus infection by upregulating the “antiviral state” of macrophages. To investigate the immunoregulatory mechanism of action of MENK on macrophages, we employed proteomic analysis to identify differentially expressed proteins (DEPs) between macrophages infected with the influenza-A virus and cells infected with the influenza-A virus after pretreatment with MENK. A total of 215 DEPs were identified: 164 proteins had upregulated expression and 51 proteins had downregulated expression. Proteomics analysis showed that DEPs were highly enriched in “cytokine-cytokine receptor interaction”, “phagosome”, and “complement and coagulation cascades pathway”. Proteomics analysis revealed that MENK could be an immune modulator or prophylactic for the prevention and treatment of influenza. MENK promoted the polarization of M1 macrophages, activated inflammatory responses, and enhanced phagocytosis and killing function by upregulating opsonizing receptors. BioMed Central 2023-04-11 /pmc/articles/PMC10088144/ /pubmed/37041527 http://dx.doi.org/10.1186/s12953-023-00205-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Fu, Wenrui Xie, Zifeng Bai, Mei Zhang, Zhen Zhao, Yuanlong Tian, Jing Proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-A virus |
title | Proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-A virus |
title_full | Proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-A virus |
title_fullStr | Proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-A virus |
title_full_unstemmed | Proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-A virus |
title_short | Proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-A virus |
title_sort | proteomics analysis of methionine enkephalin upregulated macrophages against infection by the influenza-a virus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088144/ https://www.ncbi.nlm.nih.gov/pubmed/37041527 http://dx.doi.org/10.1186/s12953-023-00205-w |
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