G-protein-coupled receptor expression, function, and signaling in macrophages (original) (raw)
Journal Article
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Cooperative Research Centre for Chronic Inflammatory Diseases, University of Queensland
,
Brisbane, Queensland
,
Australia
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Division of Cardiology, Duke University Medical Center
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Durham, North Carolina
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USA
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Cooperative Research Centre for Chronic Inflammatory Diseases, University of Queensland
,
Brisbane, Queensland
,
Australia
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Cooperative Research Centre for Chronic Inflammatory Diseases, University of Queensland
,
Brisbane, Queensland
,
Australia
School of Molecular and Microbial Sciences, University of Queensland
,
Brisbane, Queensland
,
Australia
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Cooperative Research Centre for Chronic Inflammatory Diseases, University of Queensland
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Brisbane, Queensland
,
Australia
Special Research Centre for Functional and Applied Genomics, Institute for Molecular Bioscience, University of Queensland
,
Brisbane, Queensland
,
Australia
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Cooperative Research Centre for Chronic Inflammatory Diseases, University of Queensland
,
Brisbane, Queensland
,
Australia
School of Molecular and Microbial Sciences, University of Queensland
,
Brisbane, Queensland
,
Australia
Correspondence: Institute for Molecular Bioscience, University of Queensland, St. Lucia, Brisbane, QLD 4072, Australia. E-mail: m.sweet@imb.uq.edu.au
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Received:
22 January 2007
Revision received:
29 March 2007
Cite
Jane Lattin, David A Zidar, Kate Schroder, Stuart Kellie, David A Hume, Matthew J Sweet, G-protein-coupled receptor expression, function, and signaling in macrophages, Journal of Leukocyte Biology, Volume 82, Issue 1, July 2007, Pages 16–32, https://doi.org/10.1189/jlb.0107051
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Abstract
G-protein-coupled receptors (GPCRs) are widely targeted in drug discovery. As macrophages are key cellular mediators of acute and chronic inflammation, we review here the role of GPCRs in regulating macrophage function, with a focus on contribution to disease pathology and potential therapeutic applications. Within this analysis, we highlight novel GPCRs with a macrophage-restricted expression profile, which provide avenues for further exploration. We also review an emerging literature, which documents novel roles for GPCR signaling components in GPCR-independent signaling in macrophages. In particular, we examine the crosstalk between GPCR and TLR signaling pathways and highlight GPCR signaling molecules which are likely to have uncharacterized functions in this cell lineage.
© 2007 Society for Leukocyte Biology
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