Biology:CCR2
Generic protein structure example |
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 CC 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
Alzheimer
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]
Obesity
Within the fat (adipose) tissue of CCR2 deficient mice, there is an increased number of eosinophils, greater alternative macrophage activation, and a propensity towards type 2 cytokine expression. Furthermore, this effect was exaggerated when the mice became obese from a high fat diet.[5]
Myocardial Infarct
CCR2 surface expression on blood monocytes changes in a time-of-day–dependent manner (being higher at the beginning of the active phase) and affects monocytes recruitment in tissues including the heart. As a consequence when an acute ischemic event happens during the active phase, monocytes are more susceptible to invade the heart.[6] An excessive monocytes infiltration generates higher inflammation and increases the risk of heart failure.
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).[7] 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
- ↑ 1.0 1.1 1.2 "Entrez Gene: CCR2 chemokine (C-C motif) receptor 2". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1231.
- ↑ 2.0 2.1 "Ccr2 deficiency impairs microglial accumulation and accelerates progression of Alzheimer-like disease". Nature Medicine 13 (4): 432–8. April 2007. doi:10.1038/nm1555. PMID 17351623.
- ↑ "Animal models of amyloid-beta-related pathologies in Alzheimer's disease". The FEBS Journal 277 (6): 1389–409. March 2010. doi:10.1111/j.1742-4658.2010.07564.x. PMID 20136653.
- ↑ "Role of inflammation in cognitive impairment: results of observational epidemiological studies and clinical trials". Annals of the New York Academy of Sciences 1207 (1): 155–62. October 2010. doi:10.1111/j.1749-6632.2010.05726.x. PMID 20955439. Bibcode: 2010NYASA1207..155G.
- ↑ "CCR2 deficiency leads to increased eosinophils, alternative macrophage activation, and type 2 cytokine expression in adipose tissue". Journal of Leukocyte Biology 98 (4): 467–77. October 2015. doi:10.1189/jlb.3HI0115-018R. PMID 25934927. PMC 4763864. http://www.jleukbio.org/content/98/4/467.long. Retrieved 2016-09-08.
- ↑ "Ly6C(high) Monocytes Oscillate in the Heart During Homeostasis and After Myocardial Infarction". Arteriosclerosis, Thrombosis, and Vascular Biology 37 (9): 1640–1645. June 2017. doi:10.1161/ATVBAHA.117.309259. PMID 28663258.
- ↑ "Leukocyte CCR2 expression is associated with mini-mental state examination score in older adults". Rejuvenation Research 15 (4): 395–404. August 2012. doi:10.1089/rej.2011.1302. PMID 22607625.
Further reading
- "MCP-1 and CCR2 in HIV infection: regulation of agonist and receptor expression". Journal of Leukocyte Biology 62 (1): 30–3. July 1997. doi:10.1002/jlb.62.1.30. PMID 9225989.
- "Structural interactions between chemokine receptors, gp120 Env and CD4". Seminars in Immunology 10 (3): 249–57. June 1998. doi:10.1006/smim.1998.0127. PMID 9653051.
- "The level of HIV infection of macrophages is determined by interaction of viral and host cell genotypes". Journal of Leukocyte Biology 68 (3): 311–7. September 2000. doi:10.1189/jlb.68.3.311. PMID 10985245.
- "HIV-1 infection and chemokine receptor modulation". Current HIV Research 2 (1): 39–50. January 2004. doi:10.2174/1570162043484997. PMID 15053339.
- "cDNA cloning and functional expression of a human monocyte chemoattractant protein 1 receptor". Biochemical and Biophysical Research Communications 202 (2): 1156–62. July 1994. doi:10.1006/bbrc.1994.2049. PMID 8048929.
- "Molecular cloning and functional expression of two monocyte chemoattractant protein 1 receptors reveals alternative splicing of the carboxyl-terminal tails". Proceedings of the National Academy of Sciences of the United States of America 91 (7): 2752–6. March 1994. doi:10.1073/pnas.91.7.2752. PMID 8146186. Bibcode: 1994PNAS...91.2752C.
- "Monocyte chemoattractant protein-3 is a functional ligand for CC chemokine receptors 1 and 2B". The Journal of Biological Chemistry 270 (50): 29671–5. December 1995. doi:10.1074/jbc.270.50.29671. PMID 8530354.
- "The genes encoding the human CC-chemokine receptors CC-CKR1 to CC-CKR5 (CMKBR1-CMKBR5) are clustered in the p21.3-p24 region of chromosome 3". Genomics 36 (3): 522–6. September 1996. doi:10.1006/geno.1996.0498. PMID 8884276.
- "Organization and differential expression of the human monocyte chemoattractant protein 1 receptor gene. Evidence for the role of the carboxyl-terminal tail in receptor trafficking". The Journal of Biological Chemistry 272 (2): 1038–45. January 1997. doi:10.1074/jbc.272.2.1038. PMID 8995400.
- "IL-2-regulated expression of the monocyte chemotactic protein-1 receptor (CCR2) in human NK cells: characterization of a predominant 3.4-kilobase transcript containing CCR2B and CCR2A sequences". Journal of Immunology 158 (6): 2689–94. March 1997. doi:10.4049/jimmunol.158.6.2689. PMID 9058802.
- "Expression of Tmem119/Sall1 and Ccr2/CD69 in FACS-Sorted Microglia- and Monocyte/Macrophage-Enriched Cell Populations After Intracerebral Hemorrhage". Front Cell Neurosci 12: 520. January 2019. doi:10.3389/fncel.2018.00520. PMID 30687011.
- "Monocyte chemotactic protein-2 (MCP-2) uses CCR1 and CCR2B as its functional receptors". The Journal of Biological Chemistry 272 (18): 11682–5. May 1997. doi:10.1074/jbc.272.18.11682. PMID 9115216.
- "The beta-chemokine receptor genes CCR1 (CMKBR1), CCR2 (CMKBR2), and CCR3 (CMKBR3) cluster within 285 kb on human chromosome 3p21". Genomics 41 (2): 294–5. April 1997. doi:10.1006/geno.1997.4626. PMID 9143512.
- "Cloning, in vitro expression, and functional characterization of a novel human CC chemokine of the monocyte chemotactic protein (MCP) family (MCP-4) that binds and signals through the CC chemokine receptor 2B". The Journal of Biological Chemistry 272 (26): 16404–13. June 1997. doi:10.1074/jbc.272.26.16404. PMID 9195948.
- "Contrasting genetic influence of CCR2 and CCR5 variants on HIV-1 infection and disease progression. Hemophilia Growth and Development Study (HGDS), Multicenter AIDS Cohort Study (MACS), Multicenter Hemophilia Cohort Study (MHCS), San Francisco City Cohort (SFCC), ALIVE Study". Science 277 (5328): 959–65. August 1997. doi:10.1126/science.277.5328.959. PMID 9252328.
- "The amino-terminal domain of CCR2 is both necessary and sufficient for high affinity binding of monocyte chemoattractant protein 1. Receptor activation by a pseudo-tethered ligand". The Journal of Biological Chemistry 272 (37): 23186–90. September 1997. doi:10.1074/jbc.272.37.23186. PMID 9287323.
- "Monocyte chemoattractant protein-1-induced CCR2B receptor desensitization mediated by the G protein-coupled receptor kinase 2". Proceedings of the National Academy of Sciences of the United States of America 95 (6): 2985–90. March 1998. doi:10.1073/pnas.95.6.2985. PMID 9501202. Bibcode: 1998PNAS...95.2985A.
- "Characterization of the CCR2 chemokine receptor: functional CCR2 receptor expression in B cells". Journal of Immunology 159 (11): 5576–84. December 1997. doi:10.4049/jimmunol.159.11.5576. PMID 9548499.
- "Genealogy of the CCR5 locus and chemokine system gene variants associated with altered rates of HIV-1 disease progression". Nature Medicine 4 (7): 786–93. July 1998. doi:10.1038/nm0798-786. PMID 9662369.
External links
- Human CCR2 genome location and CCR2 gene details page in the UCSC Genome Browser.
- "Chemokine Receptors: CCR2". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. http://www.iuphar-db.org/GPCR/ReceptorDisplayForward?receptorID=2222.
- CCR2+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)
- description at Information Hyperlinked Over Proteins
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
Original source: https://en.wikipedia.org/wiki/CCR2.
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