Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1782239549159636992 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3409161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wylliedavidh identificationof34novelproinflammatoryproteinsinagenomewidemacrophagefunctionalscreen AT søgaardkarenc identificationof34novelproinflammatoryproteinsinagenomewidemacrophagefunctionalscreen AT hollandkaren identificationof34novelproinflammatoryproteinsinagenomewidemacrophagefunctionalscreen AT yaoboxu identificationof34novelproinflammatoryproteinsinagenomewidemacrophagefunctionalscreen AT bregumigena identificationof34novelproinflammatoryproteinsinagenomewidemacrophagefunctionalscreen AT hilladrianvs identificationof34novelproinflammatoryproteinsinagenomewidemacrophagefunctionalscreen AT kisstothendre identificationof34novelproinflammatoryproteinsinagenomewidemacrophagefunctionalscreen |