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Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses

The innate immune system senses microbial ligands through pattern recognition and triggers downstream signaling cascades to promote inflammation and immune defense mechanisms. Emerging evidence suggests that cells also recognize alterations in host processes induced by infection as triggers. Protein...

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Autores principales: Charbonneau, Marie-Eve, Passalacqua, Karla D., Hagen, Susan E., Showalter, Hollis D., Wobus, Christiane E., O’Riordan, Mary X. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629656/
https://www.ncbi.nlm.nih.gov/pubmed/31308397
http://dx.doi.org/10.1038/s41598-019-46526-9
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author Charbonneau, Marie-Eve
Passalacqua, Karla D.
Hagen, Susan E.
Showalter, Hollis D.
Wobus, Christiane E.
O’Riordan, Mary X. D.
author_facet Charbonneau, Marie-Eve
Passalacqua, Karla D.
Hagen, Susan E.
Showalter, Hollis D.
Wobus, Christiane E.
O’Riordan, Mary X. D.
author_sort Charbonneau, Marie-Eve
collection PubMed
description The innate immune system senses microbial ligands through pattern recognition and triggers downstream signaling cascades to promote inflammation and immune defense mechanisms. Emerging evidence suggests that cells also recognize alterations in host processes induced by infection as triggers. Protein ubiquitination and deubiquitination are post-translational modification processes essential for signaling and maintenance of cellular homeostasis, and infections can cause global alterations in the host ubiquitin proteome. Here we used a chemical biology approach to perturb the cellular ubiquitin proteome as a simplified model to study the impact of ubiquitin homeostasis alteration on macrophage function. Perturbation of ubiquitin homeostasis led to a rapid and transient burst of reactive oxygen species (ROS) that promoted macrophage inflammatory and anti-infective capacity. Moreover, we found that ROS production was dependent on the NOX2 phagocyte NADPH oxidase. Global alteration of the ubiquitin proteome also enhanced proinflammatory cytokine production in mice stimulated with a sub-lethal dose of LPS. Collectively, our findings suggest that major changes in the host ubiquitin landscape may be a potent signal to rapidly deploy innate immune defenses.
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spelling pubmed-66296562019-07-23 Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses Charbonneau, Marie-Eve Passalacqua, Karla D. Hagen, Susan E. Showalter, Hollis D. Wobus, Christiane E. O’Riordan, Mary X. D. Sci Rep Article The innate immune system senses microbial ligands through pattern recognition and triggers downstream signaling cascades to promote inflammation and immune defense mechanisms. Emerging evidence suggests that cells also recognize alterations in host processes induced by infection as triggers. Protein ubiquitination and deubiquitination are post-translational modification processes essential for signaling and maintenance of cellular homeostasis, and infections can cause global alterations in the host ubiquitin proteome. Here we used a chemical biology approach to perturb the cellular ubiquitin proteome as a simplified model to study the impact of ubiquitin homeostasis alteration on macrophage function. Perturbation of ubiquitin homeostasis led to a rapid and transient burst of reactive oxygen species (ROS) that promoted macrophage inflammatory and anti-infective capacity. Moreover, we found that ROS production was dependent on the NOX2 phagocyte NADPH oxidase. Global alteration of the ubiquitin proteome also enhanced proinflammatory cytokine production in mice stimulated with a sub-lethal dose of LPS. Collectively, our findings suggest that major changes in the host ubiquitin landscape may be a potent signal to rapidly deploy innate immune defenses. Nature Publishing Group UK 2019-07-15 /pmc/articles/PMC6629656/ /pubmed/31308397 http://dx.doi.org/10.1038/s41598-019-46526-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Charbonneau, Marie-Eve
Passalacqua, Karla D.
Hagen, Susan E.
Showalter, Hollis D.
Wobus, Christiane E.
O’Riordan, Mary X. D.
Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses
title Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses
title_full Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses
title_fullStr Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses
title_full_unstemmed Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses
title_short Perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses
title_sort perturbation of ubiquitin homeostasis promotes macrophage oxidative defenses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629656/
https://www.ncbi.nlm.nih.gov/pubmed/31308397
http://dx.doi.org/10.1038/s41598-019-46526-9
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