Viral dosing of influenza A infection reveals involvement of RIPK3 and FADD, but not MLKL

Abstract RIPK3 was reported to play an important role in the protection against influenza A virus (IAV) in vivo. Here we show that the requirement of RIPK3 for protection against IAV infection in vivo is only apparent within a limited dose range of IAV challenge. We found that this protective outcom...

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Main Authors: Teodora Oltean, Emily Van San, Tatyana Divert, Tom Vanden Berghe, Xavier Saelens, Jonathan Maelfait, Nozomi Takahashi, Peter Vandenabeele
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Cell Death and Disease
Online Access:https://doi.org/10.1038/s41419-021-03746-0
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spelling doaj-4f570344a81f4a55a00c848bf43526222021-05-16T11:04:42ZengNature Publishing GroupCell Death and Disease2041-48892021-05-0112511010.1038/s41419-021-03746-0Viral dosing of influenza A infection reveals involvement of RIPK3 and FADD, but not MLKLTeodora Oltean0Emily Van San1Tatyana Divert2Tom Vanden Berghe3Xavier Saelens4Jonathan Maelfait5Nozomi Takahashi6Peter Vandenabeele7VIB-UGent Center for Inflammation ResearchVIB-UGent Center for Inflammation ResearchVIB-UGent Center for Inflammation ResearchVIB-UGent Center for Inflammation ResearchDepartment of Biomedical Molecular Biology, Ghent UniversityVIB-UGent Center for Inflammation ResearchVIB-UGent Center for Inflammation ResearchVIB-UGent Center for Inflammation ResearchAbstract RIPK3 was reported to play an important role in the protection against influenza A virus (IAV) in vivo. Here we show that the requirement of RIPK3 for protection against IAV infection in vivo is only apparent within a limited dose range of IAV challenge. We found that this protective outcome is independent from RIPK3 kinase activity and from MLKL. This shows that platform function of RIPK3 rather than its kinase activity is required for protection, suggesting that a RIPK3 function independent of necroptosis is implicated. In line with this finding, we show that FADD-dependent apoptosis has a crucial additional effect in protection against IAV infection. Altogether, we show that RIPK3 contributes to protection against IAV in a narrow challenge dose range by a mechanism that is independent of its kinase activity and its capacity to induce necroptosis.https://doi.org/10.1038/s41419-021-03746-0
collection DOAJ
language English
format Article
sources DOAJ
author Teodora Oltean
Emily Van San
Tatyana Divert
Tom Vanden Berghe
Xavier Saelens
Jonathan Maelfait
Nozomi Takahashi
Peter Vandenabeele
spellingShingle Teodora Oltean
Emily Van San
Tatyana Divert
Tom Vanden Berghe
Xavier Saelens
Jonathan Maelfait
Nozomi Takahashi
Peter Vandenabeele
Viral dosing of influenza A infection reveals involvement of RIPK3 and FADD, but not MLKL
Cell Death and Disease
author_facet Teodora Oltean
Emily Van San
Tatyana Divert
Tom Vanden Berghe
Xavier Saelens
Jonathan Maelfait
Nozomi Takahashi
Peter Vandenabeele
author_sort Teodora Oltean
title Viral dosing of influenza A infection reveals involvement of RIPK3 and FADD, but not MLKL
title_short Viral dosing of influenza A infection reveals involvement of RIPK3 and FADD, but not MLKL
title_full Viral dosing of influenza A infection reveals involvement of RIPK3 and FADD, but not MLKL
title_fullStr Viral dosing of influenza A infection reveals involvement of RIPK3 and FADD, but not MLKL
title_full_unstemmed Viral dosing of influenza A infection reveals involvement of RIPK3 and FADD, but not MLKL
title_sort viral dosing of influenza a infection reveals involvement of ripk3 and fadd, but not mlkl
publisher Nature Publishing Group
series Cell Death and Disease
issn 2041-4889
publishDate 2021-05-01
description Abstract RIPK3 was reported to play an important role in the protection against influenza A virus (IAV) in vivo. Here we show that the requirement of RIPK3 for protection against IAV infection in vivo is only apparent within a limited dose range of IAV challenge. We found that this protective outcome is independent from RIPK3 kinase activity and from MLKL. This shows that platform function of RIPK3 rather than its kinase activity is required for protection, suggesting that a RIPK3 function independent of necroptosis is implicated. In line with this finding, we show that FADD-dependent apoptosis has a crucial additional effect in protection against IAV infection. Altogether, we show that RIPK3 contributes to protection against IAV in a narrow challenge dose range by a mechanism that is independent of its kinase activity and its capacity to induce necroptosis.
url https://doi.org/10.1038/s41419-021-03746-0
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