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Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen

Signal transduction pathways activated by Toll-like Receptors and the IL-1 family of cytokines are fundamental to mounting an innate immune response and thus to clearing pathogens and promoting wound healing. Whilst mechanistic understanding of the regulation of innate signalling pathways has advanc...

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Detalles Bibliográficos
Autores principales: Wyllie, David H., Søgaard, Karen C., Holland, Karen, Yaobo, Xu, Bregu, Migena, Hill, Adrian V. S., Kiss-Toth, Endre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409161/
https://www.ncbi.nlm.nih.gov/pubmed/22860121
http://dx.doi.org/10.1371/journal.pone.0042388
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author Wyllie, David H.
Søgaard, Karen C.
Holland, Karen
Yaobo, Xu
Bregu, Migena
Hill, Adrian V. S.
Kiss-Toth, Endre
author_facet Wyllie, David H.
Søgaard, Karen C.
Holland, Karen
Yaobo, Xu
Bregu, Migena
Hill, Adrian V. S.
Kiss-Toth, Endre
author_sort Wyllie, David H.
collection PubMed
description Signal transduction pathways activated by Toll-like Receptors and the IL-1 family of cytokines are fundamental to mounting an innate immune response and thus to clearing pathogens and promoting wound healing. Whilst mechanistic understanding of the regulation of innate signalling pathways has advanced considerably in recent years, there are still a number of critical controllers to be discovered. In order to characterise novel regulators of macrophage inflammation, we have carried out an extensive, cDNA-based forward genetic screen and identified 34 novel activators, based on their ability to induce the expression of cxcl2. Many are physiologically expressed in macrophages, although the majority of genes uncovered in our screen have not previously been linked to innate immunity. We show that expression of particular activators has profound but distinct impacts on LPS-induced inflammatory gene expression, including switch-type, amplifier and sensitiser behaviours. Furthermore, the novel genes identified here interact with the canonical inflammatory signalling network via specific mechanisms, as demonstrated by the use of dominant negative forms of IL1/TLR signalling mediators.
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spelling pubmed-34091612012-08-02 Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen Wyllie, David H. Søgaard, Karen C. Holland, Karen Yaobo, Xu Bregu, Migena Hill, Adrian V. S. Kiss-Toth, Endre PLoS One Research Article Signal transduction pathways activated by Toll-like Receptors and the IL-1 family of cytokines are fundamental to mounting an innate immune response and thus to clearing pathogens and promoting wound healing. Whilst mechanistic understanding of the regulation of innate signalling pathways has advanced considerably in recent years, there are still a number of critical controllers to be discovered. In order to characterise novel regulators of macrophage inflammation, we have carried out an extensive, cDNA-based forward genetic screen and identified 34 novel activators, based on their ability to induce the expression of cxcl2. Many are physiologically expressed in macrophages, although the majority of genes uncovered in our screen have not previously been linked to innate immunity. We show that expression of particular activators has profound but distinct impacts on LPS-induced inflammatory gene expression, including switch-type, amplifier and sensitiser behaviours. Furthermore, the novel genes identified here interact with the canonical inflammatory signalling network via specific mechanisms, as demonstrated by the use of dominant negative forms of IL1/TLR signalling mediators. Public Library of Science 2012-07-31 /pmc/articles/PMC3409161/ /pubmed/22860121 http://dx.doi.org/10.1371/journal.pone.0042388 Text en © 2012 Wyllie et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wyllie, David H.
Søgaard, Karen C.
Holland, Karen
Yaobo, Xu
Bregu, Migena
Hill, Adrian V. S.
Kiss-Toth, Endre
Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen
title Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen
title_full Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen
title_fullStr Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen
title_full_unstemmed Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen
title_short Identification of 34 Novel Proinflammatory Proteins in a Genome-Wide Macrophage Functional Screen
title_sort identification of 34 novel proinflammatory proteins in a genome-wide macrophage functional screen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409161/
https://www.ncbi.nlm.nih.gov/pubmed/22860121
http://dx.doi.org/10.1371/journal.pone.0042388
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