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Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice
Macrophage scavenger receptor 1 (MSR1) mediates the endocytosis of modified low-density lipoproteins and plays an important antiviral role. However, the molecular mechanism underlying MSR1 antiviral actions remains elusive. We report that MSR1 activates autophagy to restrict infection of Chikungunya...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545163/ https://www.ncbi.nlm.nih.gov/pubmed/33033362 http://dx.doi.org/10.1038/s42003-020-01285-6 |
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author | Yang, Long Geng, Tingting Yang, Guang Ma, Jinzhu Wang, Leilei Ketkar, Harshada Yang, Duomeng Lin, Tao Hwang, Jesse Zhu, Shu Wang, Yanlin Dai, Jianfeng You, Fuping Cheng, Gong Vella, Anthony T. Flavell, Richard. A. Fikrig, Erol Wang, Penghua |
author_facet | Yang, Long Geng, Tingting Yang, Guang Ma, Jinzhu Wang, Leilei Ketkar, Harshada Yang, Duomeng Lin, Tao Hwang, Jesse Zhu, Shu Wang, Yanlin Dai, Jianfeng You, Fuping Cheng, Gong Vella, Anthony T. Flavell, Richard. A. Fikrig, Erol Wang, Penghua |
author_sort | Yang, Long |
collection | PubMed |
description | Macrophage scavenger receptor 1 (MSR1) mediates the endocytosis of modified low-density lipoproteins and plays an important antiviral role. However, the molecular mechanism underlying MSR1 antiviral actions remains elusive. We report that MSR1 activates autophagy to restrict infection of Chikungunya virus (CHIKV), an arthritogenic alphavirus that causes acute and chronic crippling arthralgia. Msr1 expression was rapidly upregulated after CHIKV infection in mice. Msr1 knockout mice had elevated viral loads and increased susceptibility to CHIKV arthritis along with a normal type I IFN response. Induction of LC3 lipidation by CHIKV, a marker of autophagy, was reduced in Msr1(−/−) cells. Mechanistically, MSR1 interacted with ATG12 through its cytoplasmic tail and this interaction was enhanced by CHIKV nsP1 protein. MSR1 repressed CHIKV replication through ATG5-ATG12-ATG16L1 and this was dependent on the FIP200-and-WIPI2-binding domain, but not the WD40 domain of ATG16L1. Our results elucidate an antiviral role for MSR1 involving the autophagic function of ATG5-ATG12-ATG16L1. |
format | Online Article Text |
id | pubmed-7545163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75451632020-10-19 Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice Yang, Long Geng, Tingting Yang, Guang Ma, Jinzhu Wang, Leilei Ketkar, Harshada Yang, Duomeng Lin, Tao Hwang, Jesse Zhu, Shu Wang, Yanlin Dai, Jianfeng You, Fuping Cheng, Gong Vella, Anthony T. Flavell, Richard. A. Fikrig, Erol Wang, Penghua Commun Biol Article Macrophage scavenger receptor 1 (MSR1) mediates the endocytosis of modified low-density lipoproteins and plays an important antiviral role. However, the molecular mechanism underlying MSR1 antiviral actions remains elusive. We report that MSR1 activates autophagy to restrict infection of Chikungunya virus (CHIKV), an arthritogenic alphavirus that causes acute and chronic crippling arthralgia. Msr1 expression was rapidly upregulated after CHIKV infection in mice. Msr1 knockout mice had elevated viral loads and increased susceptibility to CHIKV arthritis along with a normal type I IFN response. Induction of LC3 lipidation by CHIKV, a marker of autophagy, was reduced in Msr1(−/−) cells. Mechanistically, MSR1 interacted with ATG12 through its cytoplasmic tail and this interaction was enhanced by CHIKV nsP1 protein. MSR1 repressed CHIKV replication through ATG5-ATG12-ATG16L1 and this was dependent on the FIP200-and-WIPI2-binding domain, but not the WD40 domain of ATG16L1. Our results elucidate an antiviral role for MSR1 involving the autophagic function of ATG5-ATG12-ATG16L1. Nature Publishing Group UK 2020-10-08 /pmc/articles/PMC7545163/ /pubmed/33033362 http://dx.doi.org/10.1038/s42003-020-01285-6 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yang, Long Geng, Tingting Yang, Guang Ma, Jinzhu Wang, Leilei Ketkar, Harshada Yang, Duomeng Lin, Tao Hwang, Jesse Zhu, Shu Wang, Yanlin Dai, Jianfeng You, Fuping Cheng, Gong Vella, Anthony T. Flavell, Richard. A. Fikrig, Erol Wang, Penghua Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice |
title | Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice |
title_full | Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice |
title_fullStr | Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice |
title_full_unstemmed | Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice |
title_short | Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice |
title_sort | macrophage scavenger receptor 1 controls chikungunya virus infection through autophagy in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545163/ https://www.ncbi.nlm.nih.gov/pubmed/33033362 http://dx.doi.org/10.1038/s42003-020-01285-6 |
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