Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide

<p>Abstract</p> <p>Background</p> <p>Peripheral blood mononuclear cells (PBMC) serve a sentinel role allowing the host to efficiently sense and adapt to the presence of danger signals. Herein we have directly compared the genome-level expression patterns (microarray) of...

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Main Authors: Sakthivel Bhuvaneswari, Odoms Kelli, Wong Hector R
Format: Article
Language:English
Published: BMC 2008-05-01
Series:BMC Immunology
Online Access:http://www.biomedcentral.com/1471-2172/9/24
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spelling doaj-070a3147f5e547aa96ff3a14729a9af32020-11-25T03:40:04ZengBMCBMC Immunology1471-21722008-05-01912410.1186/1471-2172-9-24Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharideSakthivel BhuvaneswariOdoms KelliWong Hector R<p>Abstract</p> <p>Background</p> <p>Peripheral blood mononuclear cells (PBMC) serve a sentinel role allowing the host to efficiently sense and adapt to the presence of danger signals. Herein we have directly compared the genome-level expression patterns (microarray) of a human PBMC model (THP-1 cells) subjected to one of two canonical danger signals, heat shock or lipopolysaccharide (LPS).</p> <p>Results and Discussion</p> <p>Based on sequential expression and statistical filters, and in comparison to control cells, we found that 3,988 genes were differentially regulated in THP-1 cells subjected to LPS stress, and 2,921 genes were differentially regulated in THP-1 cells subjected to heat shock stress. Venn analyses demonstrated that the majority of differentially regulated genes (≥ 70%) were uniquely expressed in response to one of the two danger signals. Functional analyses demonstrated that the two danger signals induced expression or repression of genes corresponding to unique pathways, molecular functions, biological processes, and gene networks. In contrast, there were 184 genes that were commonly upregulated by both stress signals, and 430 genes that were commonly downregulated by both stress signals. Interestingly, the 184 commonly upregulated genes corresponded to a gene network broadly related to inflammation, and more specifically to chemokine signaling.</p> <p>Conclusion</p> <p>These data demonstrate that the mononuclear cell responses to the canonical stress signals, heat shock and LPS, are highly divergent. However, there is a heretofore unrecognized common pattern of gene network expression corresponding to chemokine-related biology. The data also serve as a reference database for investigators in the field of stress signaling.</p> http://www.biomedcentral.com/1471-2172/9/24
collection DOAJ
language English
format Article
sources DOAJ
author Sakthivel Bhuvaneswari
Odoms Kelli
Wong Hector R
spellingShingle Sakthivel Bhuvaneswari
Odoms Kelli
Wong Hector R
Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide
BMC Immunology
author_facet Sakthivel Bhuvaneswari
Odoms Kelli
Wong Hector R
author_sort Sakthivel Bhuvaneswari
title Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide
title_short Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide
title_full Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide
title_fullStr Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide
title_full_unstemmed Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide
title_sort divergence of canonical danger signals: the genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide
publisher BMC
series BMC Immunology
issn 1471-2172
publishDate 2008-05-01
description <p>Abstract</p> <p>Background</p> <p>Peripheral blood mononuclear cells (PBMC) serve a sentinel role allowing the host to efficiently sense and adapt to the presence of danger signals. Herein we have directly compared the genome-level expression patterns (microarray) of a human PBMC model (THP-1 cells) subjected to one of two canonical danger signals, heat shock or lipopolysaccharide (LPS).</p> <p>Results and Discussion</p> <p>Based on sequential expression and statistical filters, and in comparison to control cells, we found that 3,988 genes were differentially regulated in THP-1 cells subjected to LPS stress, and 2,921 genes were differentially regulated in THP-1 cells subjected to heat shock stress. Venn analyses demonstrated that the majority of differentially regulated genes (≥ 70%) were uniquely expressed in response to one of the two danger signals. Functional analyses demonstrated that the two danger signals induced expression or repression of genes corresponding to unique pathways, molecular functions, biological processes, and gene networks. In contrast, there were 184 genes that were commonly upregulated by both stress signals, and 430 genes that were commonly downregulated by both stress signals. Interestingly, the 184 commonly upregulated genes corresponded to a gene network broadly related to inflammation, and more specifically to chemokine signaling.</p> <p>Conclusion</p> <p>These data demonstrate that the mononuclear cell responses to the canonical stress signals, heat shock and LPS, are highly divergent. However, there is a heretofore unrecognized common pattern of gene network expression corresponding to chemokine-related biology. The data also serve as a reference database for investigators in the field of stress signaling.</p>
url http://www.biomedcentral.com/1471-2172/9/24
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AT odomskelli divergenceofcanonicaldangersignalsthegenomelevelexpressionpatternsofhumanmononuclearcellssubjectedtoheatshockorlipopolysaccharide
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