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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2021-05-01
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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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