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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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.
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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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