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Impact of animal strain on gene expression in a rat model of acute cardiac rejection

BACKGROUND: The expression levels of many genes show wide natural variation among strains or populations. This study investigated the potential for animal strain-related genotypic differences to confound gene expression profiles in acute cellular rejection (ACR). Using a rat heart transplant model a...

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Autores principales: Deans, Katherine J, Minneci, Peter C, Chen, Hao, Kern, Steven J, Logun, Carolea, Alsaaty, Sara, Norsworthy, Kelly J, Theel, Stephanie M, Sennesh, Joel D, Barb, Jennifer J, Munson, Peter J, Danner, Robert L, Solomon, Michael A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711118/
https://www.ncbi.nlm.nih.gov/pubmed/19552812
http://dx.doi.org/10.1186/1471-2164-10-280
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author Deans, Katherine J
Minneci, Peter C
Chen, Hao
Kern, Steven J
Logun, Carolea
Alsaaty, Sara
Norsworthy, Kelly J
Theel, Stephanie M
Sennesh, Joel D
Barb, Jennifer J
Munson, Peter J
Danner, Robert L
Solomon, Michael A
author_facet Deans, Katherine J
Minneci, Peter C
Chen, Hao
Kern, Steven J
Logun, Carolea
Alsaaty, Sara
Norsworthy, Kelly J
Theel, Stephanie M
Sennesh, Joel D
Barb, Jennifer J
Munson, Peter J
Danner, Robert L
Solomon, Michael A
author_sort Deans, Katherine J
collection PubMed
description BACKGROUND: The expression levels of many genes show wide natural variation among strains or populations. This study investigated the potential for animal strain-related genotypic differences to confound gene expression profiles in acute cellular rejection (ACR). Using a rat heart transplant model and 2 different rat strains (Dark Agouti, and Brown Norway), microarrays were performed on native hearts, transplanted hearts, and peripheral blood mononuclear cells (PBMC). RESULTS: In heart tissue, strain alone affected the expression of only 33 probesets while rejection affected the expression of 1368 probesets (FDR 10% and FC ≥ 3). Only 13 genes were affected by both strain and rejection, which was < 1% (13/1368) of all probesets differentially expressed in ACR. However, for PBMC, strain alone affected 265 probesets (FDR 10% and FC ≥ 3) and the addition of ACR had little further effect. Pathway analysis of these differentially expressed strain effect genes connected them with immune response, cell motility and cell death, functional themes that overlap with those related to ACR. After accounting for animal strain, additional analysis identified 30 PBMC candidate genes potentially associated with ACR. CONCLUSION: In ACR, genetic background has a large impact on the transcriptome of immune cells, but not heart tissue. Gene expression studies of ACR should avoid study designs that require cross strain comparisons between leukocytes.
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spelling pubmed-27111182009-07-16 Impact of animal strain on gene expression in a rat model of acute cardiac rejection Deans, Katherine J Minneci, Peter C Chen, Hao Kern, Steven J Logun, Carolea Alsaaty, Sara Norsworthy, Kelly J Theel, Stephanie M Sennesh, Joel D Barb, Jennifer J Munson, Peter J Danner, Robert L Solomon, Michael A BMC Genomics Research Article BACKGROUND: The expression levels of many genes show wide natural variation among strains or populations. This study investigated the potential for animal strain-related genotypic differences to confound gene expression profiles in acute cellular rejection (ACR). Using a rat heart transplant model and 2 different rat strains (Dark Agouti, and Brown Norway), microarrays were performed on native hearts, transplanted hearts, and peripheral blood mononuclear cells (PBMC). RESULTS: In heart tissue, strain alone affected the expression of only 33 probesets while rejection affected the expression of 1368 probesets (FDR 10% and FC ≥ 3). Only 13 genes were affected by both strain and rejection, which was < 1% (13/1368) of all probesets differentially expressed in ACR. However, for PBMC, strain alone affected 265 probesets (FDR 10% and FC ≥ 3) and the addition of ACR had little further effect. Pathway analysis of these differentially expressed strain effect genes connected them with immune response, cell motility and cell death, functional themes that overlap with those related to ACR. After accounting for animal strain, additional analysis identified 30 PBMC candidate genes potentially associated with ACR. CONCLUSION: In ACR, genetic background has a large impact on the transcriptome of immune cells, but not heart tissue. Gene expression studies of ACR should avoid study designs that require cross strain comparisons between leukocytes. BioMed Central 2009-06-24 /pmc/articles/PMC2711118/ /pubmed/19552812 http://dx.doi.org/10.1186/1471-2164-10-280 Text en Copyright © 2009 Deans et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Deans, Katherine J
Minneci, Peter C
Chen, Hao
Kern, Steven J
Logun, Carolea
Alsaaty, Sara
Norsworthy, Kelly J
Theel, Stephanie M
Sennesh, Joel D
Barb, Jennifer J
Munson, Peter J
Danner, Robert L
Solomon, Michael A
Impact of animal strain on gene expression in a rat model of acute cardiac rejection
title Impact of animal strain on gene expression in a rat model of acute cardiac rejection
title_full Impact of animal strain on gene expression in a rat model of acute cardiac rejection
title_fullStr Impact of animal strain on gene expression in a rat model of acute cardiac rejection
title_full_unstemmed Impact of animal strain on gene expression in a rat model of acute cardiac rejection
title_short Impact of animal strain on gene expression in a rat model of acute cardiac rejection
title_sort impact of animal strain on gene expression in a rat model of acute cardiac rejection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711118/
https://www.ncbi.nlm.nih.gov/pubmed/19552812
http://dx.doi.org/10.1186/1471-2164-10-280
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