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Expression analysis of G Protein-Coupled Receptors in mouse macrophages
BACKGROUND: Monocytes and macrophages express an extensive repertoire of G Protein-Coupled Receptors (GPCRs) that regulate inflammation and immunity. In this study we performed a systematic micro-array analysis of GPCR expression in primary mouse macrophages to identify family members that are eithe...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394514/ https://www.ncbi.nlm.nih.gov/pubmed/18442421 http://dx.doi.org/10.1186/1745-7580-4-5 |
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author | Lattin, Jane E Schroder, Kate Su, Andrew I Walker, John R Zhang, Jie Wiltshire, Tim Saijo, Kaoru Glass, Christopher K Hume, David A Kellie, Stuart Sweet, Matthew J |
author_facet | Lattin, Jane E Schroder, Kate Su, Andrew I Walker, John R Zhang, Jie Wiltshire, Tim Saijo, Kaoru Glass, Christopher K Hume, David A Kellie, Stuart Sweet, Matthew J |
author_sort | Lattin, Jane E |
collection | PubMed |
description | BACKGROUND: Monocytes and macrophages express an extensive repertoire of G Protein-Coupled Receptors (GPCRs) that regulate inflammation and immunity. In this study we performed a systematic micro-array analysis of GPCR expression in primary mouse macrophages to identify family members that are either enriched in macrophages compared to a panel of other cell types, or are regulated by an inflammatory stimulus, the bacterial product lipopolysaccharide (LPS). RESULTS: Several members of the P2RY family had striking expression patterns in macrophages; P2ry6 mRNA was essentially expressed in a macrophage-specific fashion, whilst P2ry1 and P2ry5 mRNA levels were strongly down-regulated by LPS. Expression of several other GPCRs was either restricted to macrophages (e.g. Gpr84) or to both macrophages and neural tissues (e.g. P2ry12, Gpr85). The GPCR repertoire expressed by bone marrow-derived macrophages and thioglycollate-elicited peritoneal macrophages had some commonality, but there were also several GPCRs preferentially expressed by either cell population. CONCLUSION: The constitutive or regulated expression in macrophages of several GPCRs identified in this study has not previously been described. Future studies on such GPCRs and their agonists are likely to provide important insights into macrophage biology, as well as novel inflammatory pathways that could be future targets for drug discovery. |
format | Text |
id | pubmed-2394514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23945142008-05-23 Expression analysis of G Protein-Coupled Receptors in mouse macrophages Lattin, Jane E Schroder, Kate Su, Andrew I Walker, John R Zhang, Jie Wiltshire, Tim Saijo, Kaoru Glass, Christopher K Hume, David A Kellie, Stuart Sweet, Matthew J Immunome Res Research BACKGROUND: Monocytes and macrophages express an extensive repertoire of G Protein-Coupled Receptors (GPCRs) that regulate inflammation and immunity. In this study we performed a systematic micro-array analysis of GPCR expression in primary mouse macrophages to identify family members that are either enriched in macrophages compared to a panel of other cell types, or are regulated by an inflammatory stimulus, the bacterial product lipopolysaccharide (LPS). RESULTS: Several members of the P2RY family had striking expression patterns in macrophages; P2ry6 mRNA was essentially expressed in a macrophage-specific fashion, whilst P2ry1 and P2ry5 mRNA levels were strongly down-regulated by LPS. Expression of several other GPCRs was either restricted to macrophages (e.g. Gpr84) or to both macrophages and neural tissues (e.g. P2ry12, Gpr85). The GPCR repertoire expressed by bone marrow-derived macrophages and thioglycollate-elicited peritoneal macrophages had some commonality, but there were also several GPCRs preferentially expressed by either cell population. CONCLUSION: The constitutive or regulated expression in macrophages of several GPCRs identified in this study has not previously been described. Future studies on such GPCRs and their agonists are likely to provide important insights into macrophage biology, as well as novel inflammatory pathways that could be future targets for drug discovery. BioMed Central 2008-04-29 /pmc/articles/PMC2394514/ /pubmed/18442421 http://dx.doi.org/10.1186/1745-7580-4-5 Text en Copyright © 2008 Lattin 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 Lattin, Jane E Schroder, Kate Su, Andrew I Walker, John R Zhang, Jie Wiltshire, Tim Saijo, Kaoru Glass, Christopher K Hume, David A Kellie, Stuart Sweet, Matthew J Expression analysis of G Protein-Coupled Receptors in mouse macrophages |
title | Expression analysis of G Protein-Coupled Receptors in mouse macrophages |
title_full | Expression analysis of G Protein-Coupled Receptors in mouse macrophages |
title_fullStr | Expression analysis of G Protein-Coupled Receptors in mouse macrophages |
title_full_unstemmed | Expression analysis of G Protein-Coupled Receptors in mouse macrophages |
title_short | Expression analysis of G Protein-Coupled Receptors in mouse macrophages |
title_sort | expression analysis of g protein-coupled receptors in mouse macrophages |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394514/ https://www.ncbi.nlm.nih.gov/pubmed/18442421 http://dx.doi.org/10.1186/1745-7580-4-5 |
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