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NOD Signaling and Cell Death

Innate immune signaling and programmed cell death are intimately linked, and many signaling pathways can regulate and induce both, transcription of inflammatory mediators or autonomous cell death. The best-characterized examples for these dual outcomes are members of the TNF superfamily, the inflamm...

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Autores principales: Heim, Valentin J., Stafford, Che A., Nachbur, Ueli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783575/
https://www.ncbi.nlm.nih.gov/pubmed/31632962
http://dx.doi.org/10.3389/fcell.2019.00208
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author Heim, Valentin J.
Stafford, Che A.
Nachbur, Ueli
author_facet Heim, Valentin J.
Stafford, Che A.
Nachbur, Ueli
author_sort Heim, Valentin J.
collection PubMed
description Innate immune signaling and programmed cell death are intimately linked, and many signaling pathways can regulate and induce both, transcription of inflammatory mediators or autonomous cell death. The best-characterized examples for these dual outcomes are members of the TNF superfamily, the inflammasome receptors, and the toll-like receptors. Signaling via the intracellular peptidoglycan receptors NOD1 and NOD2, however, does not appear to follow this trend, despite involving signaling proteins, or proteins with domains that are linked to programmed cell death, such as RIP kinases, inhibitors of apoptosis (IAP) proteins or the CARD domains on NOD1/2. To better understand the connections between NOD signaling and cell death induction, we here review the latest findings on the molecular regulation of signaling downstream of the NOD receptors and explore the links between this immune signaling pathway and the regulation of cell death.
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spelling pubmed-67835752019-10-18 NOD Signaling and Cell Death Heim, Valentin J. Stafford, Che A. Nachbur, Ueli Front Cell Dev Biol Cell and Developmental Biology Innate immune signaling and programmed cell death are intimately linked, and many signaling pathways can regulate and induce both, transcription of inflammatory mediators or autonomous cell death. The best-characterized examples for these dual outcomes are members of the TNF superfamily, the inflammasome receptors, and the toll-like receptors. Signaling via the intracellular peptidoglycan receptors NOD1 and NOD2, however, does not appear to follow this trend, despite involving signaling proteins, or proteins with domains that are linked to programmed cell death, such as RIP kinases, inhibitors of apoptosis (IAP) proteins or the CARD domains on NOD1/2. To better understand the connections between NOD signaling and cell death induction, we here review the latest findings on the molecular regulation of signaling downstream of the NOD receptors and explore the links between this immune signaling pathway and the regulation of cell death. Frontiers Media S.A. 2019-10-02 /pmc/articles/PMC6783575/ /pubmed/31632962 http://dx.doi.org/10.3389/fcell.2019.00208 Text en Copyright © 2019 Heim, Stafford and Nachbur. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Heim, Valentin J.
Stafford, Che A.
Nachbur, Ueli
NOD Signaling and Cell Death
title NOD Signaling and Cell Death
title_full NOD Signaling and Cell Death
title_fullStr NOD Signaling and Cell Death
title_full_unstemmed NOD Signaling and Cell Death
title_short NOD Signaling and Cell Death
title_sort nod signaling and cell death
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783575/
https://www.ncbi.nlm.nih.gov/pubmed/31632962
http://dx.doi.org/10.3389/fcell.2019.00208
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