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Development and validation of a bovine macrophage specific cDNA microarray

BACKGROUND: The response of macrophages to danger signals is an important early stage in the immune response. Our understanding of this complex event has been furthered by microarray analysis, which allows the simultaneous investigation of the expression of large numbers of genes. However, the micro...

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Autores principales: Jensen, Kirsty, Talbot, Richard, Paxton, Edith, Waddington, David, Glass, Elizabeth J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1590031/
https://www.ncbi.nlm.nih.gov/pubmed/16948847
http://dx.doi.org/10.1186/1471-2164-7-224
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author Jensen, Kirsty
Talbot, Richard
Paxton, Edith
Waddington, David
Glass, Elizabeth J
author_facet Jensen, Kirsty
Talbot, Richard
Paxton, Edith
Waddington, David
Glass, Elizabeth J
author_sort Jensen, Kirsty
collection PubMed
description BACKGROUND: The response of macrophages to danger signals is an important early stage in the immune response. Our understanding of this complex event has been furthered by microarray analysis, which allows the simultaneous investigation of the expression of large numbers of genes. However, the microarray resources available to study these events in livestock animals are limited. RESULTS: Here we report the development of a bovine macrophage specific (BoMP) cDNA microarray. The BoMP microarray contains 5026 sequence elements (printed in duplicate) and numerous controls. The majority of the clones incorporated on the microarray were derived from the BoMP cDNA library generated from bovine myeloid cells subjected to various stimuli, including over 900 sequences unique to the library. Additional clones representing immunologically important genes have been included on the BoMP microarray. The microarray was validated by investigating the response of bovine monocytes to stimulation with interferon-γ and lipopolysaccharide using amplified RNA. At 2 and 16 hours post stimulation 695 genes exhibited statistically significant differential expression, including; 26 sequences unique to the BoMP library, interleukin 6, prion protein and toll-like receptor 4. CONCLUSION: A 5 K cDNA microarray has been successfully developed to investigate gene expression in bovine myeloid cells. The BoMP microarray is available from the ARK-Genomics Centre for Functional Genomics in Farm Animals, UK.
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spelling pubmed-15900312006-10-05 Development and validation of a bovine macrophage specific cDNA microarray Jensen, Kirsty Talbot, Richard Paxton, Edith Waddington, David Glass, Elizabeth J BMC Genomics Research Article BACKGROUND: The response of macrophages to danger signals is an important early stage in the immune response. Our understanding of this complex event has been furthered by microarray analysis, which allows the simultaneous investigation of the expression of large numbers of genes. However, the microarray resources available to study these events in livestock animals are limited. RESULTS: Here we report the development of a bovine macrophage specific (BoMP) cDNA microarray. The BoMP microarray contains 5026 sequence elements (printed in duplicate) and numerous controls. The majority of the clones incorporated on the microarray were derived from the BoMP cDNA library generated from bovine myeloid cells subjected to various stimuli, including over 900 sequences unique to the library. Additional clones representing immunologically important genes have been included on the BoMP microarray. The microarray was validated by investigating the response of bovine monocytes to stimulation with interferon-γ and lipopolysaccharide using amplified RNA. At 2 and 16 hours post stimulation 695 genes exhibited statistically significant differential expression, including; 26 sequences unique to the BoMP library, interleukin 6, prion protein and toll-like receptor 4. CONCLUSION: A 5 K cDNA microarray has been successfully developed to investigate gene expression in bovine myeloid cells. The BoMP microarray is available from the ARK-Genomics Centre for Functional Genomics in Farm Animals, UK. BioMed Central 2006-09-01 /pmc/articles/PMC1590031/ /pubmed/16948847 http://dx.doi.org/10.1186/1471-2164-7-224 Text en Copyright © 2006 Jensen 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
Jensen, Kirsty
Talbot, Richard
Paxton, Edith
Waddington, David
Glass, Elizabeth J
Development and validation of a bovine macrophage specific cDNA microarray
title Development and validation of a bovine macrophage specific cDNA microarray
title_full Development and validation of a bovine macrophage specific cDNA microarray
title_fullStr Development and validation of a bovine macrophage specific cDNA microarray
title_full_unstemmed Development and validation of a bovine macrophage specific cDNA microarray
title_short Development and validation of a bovine macrophage specific cDNA microarray
title_sort development and validation of a bovine macrophage specific cdna microarray
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1590031/
https://www.ncbi.nlm.nih.gov/pubmed/16948847
http://dx.doi.org/10.1186/1471-2164-7-224
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