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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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