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Speculations on the activation of ROS generation in C. elegans innate immune signaling

We recently published work demonstrating that ROS (reactive oxygen species) generated by the dual oxidase, Ce-Duox1/BLI-3, in response to infection in Caenorhabditis elegans activates the transcription factor SKN-1, initiating a protective response. Moreover, we showed that the crucial innate immune...

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Autores principales: van der Hoeven, Ransome, McCallum, Katie C., Garsin, Danielle A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670408/
https://www.ncbi.nlm.nih.gov/pubmed/24058842
http://dx.doi.org/10.4161/worm.19767
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author van der Hoeven, Ransome
McCallum, Katie C.
Garsin, Danielle A.
author_facet van der Hoeven, Ransome
McCallum, Katie C.
Garsin, Danielle A.
author_sort van der Hoeven, Ransome
collection PubMed
description We recently published work demonstrating that ROS (reactive oxygen species) generated by the dual oxidase, Ce-Duox1/BLI-3, in response to infection in Caenorhabditis elegans activates the transcription factor SKN-1, initiating a protective response. Moreover, we showed that the crucial innate immune pathway, p38 MAPK signaling, was responsible for relaying the activating signal. In this commentary, we speculate on the signaling pathway upstream of Ce-Duox1/BLI-3 that triggers its activity. Specifically, we hypothesize that a G-protein signaling pathway comprising Gαq - PLCβ - TPA-1 - DKF-2 activates Ce-Duox1/BLI-3. Our rationale is based on work showing that these components are connected to p38 MAPK signaling and innate immunity in the worm, and investigations in other organisms demonstrating that some of these components are involved in dual oxidase activation.
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spelling pubmed-36704082013-09-19 Speculations on the activation of ROS generation in C. elegans innate immune signaling van der Hoeven, Ransome McCallum, Katie C. Garsin, Danielle A. Worm Commentary We recently published work demonstrating that ROS (reactive oxygen species) generated by the dual oxidase, Ce-Duox1/BLI-3, in response to infection in Caenorhabditis elegans activates the transcription factor SKN-1, initiating a protective response. Moreover, we showed that the crucial innate immune pathway, p38 MAPK signaling, was responsible for relaying the activating signal. In this commentary, we speculate on the signaling pathway upstream of Ce-Duox1/BLI-3 that triggers its activity. Specifically, we hypothesize that a G-protein signaling pathway comprising Gαq - PLCβ - TPA-1 - DKF-2 activates Ce-Duox1/BLI-3. Our rationale is based on work showing that these components are connected to p38 MAPK signaling and innate immunity in the worm, and investigations in other organisms demonstrating that some of these components are involved in dual oxidase activation. Landes Bioscience 2012-07-01 /pmc/articles/PMC3670408/ /pubmed/24058842 http://dx.doi.org/10.4161/worm.19767 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Commentary
van der Hoeven, Ransome
McCallum, Katie C.
Garsin, Danielle A.
Speculations on the activation of ROS generation in C. elegans innate immune signaling
title Speculations on the activation of ROS generation in C. elegans innate immune signaling
title_full Speculations on the activation of ROS generation in C. elegans innate immune signaling
title_fullStr Speculations on the activation of ROS generation in C. elegans innate immune signaling
title_full_unstemmed Speculations on the activation of ROS generation in C. elegans innate immune signaling
title_short Speculations on the activation of ROS generation in C. elegans innate immune signaling
title_sort speculations on the activation of ros generation in c. elegans innate immune signaling
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670408/
https://www.ncbi.nlm.nih.gov/pubmed/24058842
http://dx.doi.org/10.4161/worm.19767
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