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Ubiquitination and degradation of NF90 by Tim-3 inhibits antiviral innate immunity
Nuclear factor 90 (NF90) is a novel virus sensor that serves to initiate antiviral innate immunity by triggering stress granule (SG) formation. However, the regulation of the NF90-SG pathway remains largely unclear. We found that Tim-3, an immune checkpoint inhibitor, promotes the ubiquitination and...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225388/ https://www.ncbi.nlm.nih.gov/pubmed/34110282 http://dx.doi.org/10.7554/eLife.66501 |
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author | Dou, Shuaijie Li, Guoxian Li, Ge Hou, Chunmei Zheng, Yang Tang, Lili Gao, Yang Mo, Rongliang Li, Yuxiang Wang, Renxi Shen, Beifen Zhang, Jun Han, Gencheng |
author_facet | Dou, Shuaijie Li, Guoxian Li, Ge Hou, Chunmei Zheng, Yang Tang, Lili Gao, Yang Mo, Rongliang Li, Yuxiang Wang, Renxi Shen, Beifen Zhang, Jun Han, Gencheng |
author_sort | Dou, Shuaijie |
collection | PubMed |
description | Nuclear factor 90 (NF90) is a novel virus sensor that serves to initiate antiviral innate immunity by triggering stress granule (SG) formation. However, the regulation of the NF90-SG pathway remains largely unclear. We found that Tim-3, an immune checkpoint inhibitor, promotes the ubiquitination and degradation of NF90 and inhibits NF90-SG-mediated antiviral immunity. Vesicular stomatitis virus (VSV) infection induces the up-regulation and activation of Tim-3 in macrophages, which in turn recruit the E3 ubiquitin ligase TRIM47 to the zinc finger domain of NF90 and initiate a proteasome-dependent degradation via K48-linked ubiquitination at Lys297. Targeted inactivation of Tim-3 enhances the NF90 downstream SG formation by selectively increasing the phosphorylation of protein kinase R and eukaryotic translation initiation factor 2α, the expression of SG markers G3BP1 and TIA-1, and protecting mice from VSV challenge. These findings provide insights into the crosstalk between Tim-3 and other receptors in antiviral innate immunity and its related clinical significance. |
format | Online Article Text |
id | pubmed-8225388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-82253882021-06-28 Ubiquitination and degradation of NF90 by Tim-3 inhibits antiviral innate immunity Dou, Shuaijie Li, Guoxian Li, Ge Hou, Chunmei Zheng, Yang Tang, Lili Gao, Yang Mo, Rongliang Li, Yuxiang Wang, Renxi Shen, Beifen Zhang, Jun Han, Gencheng eLife Immunology and Inflammation Nuclear factor 90 (NF90) is a novel virus sensor that serves to initiate antiviral innate immunity by triggering stress granule (SG) formation. However, the regulation of the NF90-SG pathway remains largely unclear. We found that Tim-3, an immune checkpoint inhibitor, promotes the ubiquitination and degradation of NF90 and inhibits NF90-SG-mediated antiviral immunity. Vesicular stomatitis virus (VSV) infection induces the up-regulation and activation of Tim-3 in macrophages, which in turn recruit the E3 ubiquitin ligase TRIM47 to the zinc finger domain of NF90 and initiate a proteasome-dependent degradation via K48-linked ubiquitination at Lys297. Targeted inactivation of Tim-3 enhances the NF90 downstream SG formation by selectively increasing the phosphorylation of protein kinase R and eukaryotic translation initiation factor 2α, the expression of SG markers G3BP1 and TIA-1, and protecting mice from VSV challenge. These findings provide insights into the crosstalk between Tim-3 and other receptors in antiviral innate immunity and its related clinical significance. eLife Sciences Publications, Ltd 2021-06-10 /pmc/articles/PMC8225388/ /pubmed/34110282 http://dx.doi.org/10.7554/eLife.66501 Text en © 2021, Dou et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology and Inflammation Dou, Shuaijie Li, Guoxian Li, Ge Hou, Chunmei Zheng, Yang Tang, Lili Gao, Yang Mo, Rongliang Li, Yuxiang Wang, Renxi Shen, Beifen Zhang, Jun Han, Gencheng Ubiquitination and degradation of NF90 by Tim-3 inhibits antiviral innate immunity |
title | Ubiquitination and degradation of NF90 by Tim-3 inhibits antiviral innate immunity |
title_full | Ubiquitination and degradation of NF90 by Tim-3 inhibits antiviral innate immunity |
title_fullStr | Ubiquitination and degradation of NF90 by Tim-3 inhibits antiviral innate immunity |
title_full_unstemmed | Ubiquitination and degradation of NF90 by Tim-3 inhibits antiviral innate immunity |
title_short | Ubiquitination and degradation of NF90 by Tim-3 inhibits antiviral innate immunity |
title_sort | ubiquitination and degradation of nf90 by tim-3 inhibits antiviral innate immunity |
topic | Immunology and Inflammation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225388/ https://www.ncbi.nlm.nih.gov/pubmed/34110282 http://dx.doi.org/10.7554/eLife.66501 |
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