CCR2

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Chemokine (C-C motif) receptor 2
Protein CCR2 PDB 1KAD.png
Rendering based on PDB 1KAD.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols CCR2 ; CC-CKR-2; CCR-2; CCR2A; CCR2B; CD192; CKR2; CKR2A; CKR2B; CMKBR2; MCP-1-R
External IDs OMIM601267 MGI106185 HomoloGene537 IUPHAR: 59 GeneCards: CCR2 Gene
Orthologs
Species Human Mouse
Entrez 729230 12772
Ensembl ENSG00000121807 ENSMUSG00000049103
UniProt P41597 P51683
RefSeq (mRNA) NM_001123041 NM_009915
RefSeq (protein) NP_001116513 NP_034045
Location (UCSC) Chr 3:
46.35 – 46.36 Mb
Chr 9:
124.1 – 124.11 Mb
PubMed search [1] [2]

C-C chemokine receptor type 2 (CCR2 or CD192 (cluster of differentiation 192) is a protein that in humans is encoded by the CCR2 gene.[1] CCR2 is a chemokine receptor.

Gene

This CCR2 gene is located in the chemokine receptor gene cluster region. Two alternatively spliced transcript variants are expressed by the gene.[1]

Function

This gene encodes two isoforms of a receptor for monocyte chemoattractant protein-1 (CCL2), a chemokine which specifically mediates monocyte chemotaxis. Monocyte chemoattractant protein-1 is involved in monocyte infiltration in inflammatory diseases such as rheumatoid arthritis as well as in the inflammatory response against tumors. The receptors encoded by this gene mediate agonist-dependent calcium mobilization and inhibition of adenylyl cyclase.[1]

Animal studies

CCR2 deficient mice have been shown to develop an accelerated Alzheimer's-like pathology in comparison to wild type mice.[2][3] This is not the first time that immune function and inflammation have been linked to age-related cognitive decline (i.e. dementia).[4]

Clinical significance

In an observational study of gene expression in blood leukocytes in humans, Harries et al. found evidence of a relationship between expression of CCR2 and cognitive function (assessed using the mini-mental state examination, MMSE).[5] Higher CCR2 expression was associated with worse performance on the MMSE assessment of cognitive function. The same study found that CCR2 expression was also associated with cognitive decline over 9-years in a sub-analysis on inflammatory related transcripts only. Harries et al. suggest that CCR2 signaling may have a direct role in human cognition, partly because expression of CCR2 was associated with the ApoE haplotype (previously associated with Alzheimer's disease), but also because CCL2 is expressed at high concentrations in macrophages found in atherosclerotic plaques and in brain microglia.[2] The difference in observations between mice (CCR2 depletion causes cognitive decline) and humans (higher CCR2 associated with lower cognitive function) could be due to increased demand for macrophage activation during cognitive decline, associated with increased β-amyloid deposition (a core feature of Alzheimer's disease progression).

See also

References

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Further reading

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External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.