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Salmonella Typhimurium infection: Type I Interferons integrate cellular networks to disintegrate macrophages

Type I interferons have immunomodulatory functions during infection with bacteria and viruses. They are vital for the host defense against viruses and extracellular bacteria. However, recent evidences show that IFN-I contributes to immunopathology during intracellular bacterial infection. We had pre...

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Detalles Bibliográficos
Autor principal: Robinson, Nirmal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551721/
https://www.ncbi.nlm.nih.gov/pubmed/31225465
http://dx.doi.org/10.15698/cst2018.02.125
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author Robinson, Nirmal
author_facet Robinson, Nirmal
author_sort Robinson, Nirmal
collection PubMed
description Type I interferons have immunomodulatory functions during infection with bacteria and viruses. They are vital for the host defense against viruses and extracellular bacteria. However, recent evidences show that IFN-I contributes to immunopathology during intracellular bacterial infection. We had previously shown that IFN-I receptor knock out mice (ifnar(-/-)) are less susceptible to S. Typhimurium infection and the macrophages are resistant to S. Typhimurium-induced cell death dependent on RIP kinases commonly known as necroptosis. We have now recently shown that IFN-I-signaling through the activation of RIP kinases and PGAM5 exacerbates necroptosis in Salmonella Typhimurium-infected macrophages by downregulating Nrf2-dependent cytoprotective response mechanisms [Hos et al, JCB 2017].
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spelling pubmed-65517212019-06-20 Salmonella Typhimurium infection: Type I Interferons integrate cellular networks to disintegrate macrophages Robinson, Nirmal Cell Stress Microreview Type I interferons have immunomodulatory functions during infection with bacteria and viruses. They are vital for the host defense against viruses and extracellular bacteria. However, recent evidences show that IFN-I contributes to immunopathology during intracellular bacterial infection. We had previously shown that IFN-I receptor knock out mice (ifnar(-/-)) are less susceptible to S. Typhimurium infection and the macrophages are resistant to S. Typhimurium-induced cell death dependent on RIP kinases commonly known as necroptosis. We have now recently shown that IFN-I-signaling through the activation of RIP kinases and PGAM5 exacerbates necroptosis in Salmonella Typhimurium-infected macrophages by downregulating Nrf2-dependent cytoprotective response mechanisms [Hos et al, JCB 2017]. Shared Science Publishers OG 2018-01-30 /pmc/articles/PMC6551721/ /pubmed/31225465 http://dx.doi.org/10.15698/cst2018.02.125 Text en Copyright: © 2018 Robinson https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Microreview
Robinson, Nirmal
Salmonella Typhimurium infection: Type I Interferons integrate cellular networks to disintegrate macrophages
title Salmonella Typhimurium infection: Type I Interferons integrate cellular networks to disintegrate macrophages
title_full Salmonella Typhimurium infection: Type I Interferons integrate cellular networks to disintegrate macrophages
title_fullStr Salmonella Typhimurium infection: Type I Interferons integrate cellular networks to disintegrate macrophages
title_full_unstemmed Salmonella Typhimurium infection: Type I Interferons integrate cellular networks to disintegrate macrophages
title_short Salmonella Typhimurium infection: Type I Interferons integrate cellular networks to disintegrate macrophages
title_sort salmonella typhimurium infection: type i interferons integrate cellular networks to disintegrate macrophages
topic Microreview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551721/
https://www.ncbi.nlm.nih.gov/pubmed/31225465
http://dx.doi.org/10.15698/cst2018.02.125
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