"Receptors, CCR2" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
CCR receptors with specificity for CHEMOKINE CCL2 and several other CCL2-related chemokines. They are expressed at high levels in T-LYMPHOCYTES; B-LYMPHOCYTES; MACROPHAGES; BASOPHILS; and NK CELLS.
| Descriptor ID |
D054390
|
| MeSH Number(s) |
D12.776.543.750.695.160.150.200 D12.776.543.750.705.852.125.150.200
|
| Concept/Terms |
Receptors, CCR2- Receptors, CCR2
- MCP-1 Receptor
- MCP 1 Receptor
- Receptor, MCP-1
- MCP-1 Receptors
- MCP 1 Receptors
- Receptors, MCP-1
- Monocyte Chemoattractant Protein 1 Receptor
- CCR2 Receptor
- Receptor, CCR2
- CCR2 Receptors
- CC Chemokine Receptor 2
- CD192 Antigens
- Antigens, CD192
- CC Chemokine Receptor-2
- Chemokine Receptor-2, CC
- Receptor-2, CC Chemokine
- CC Chemokine Receptors 2
CCR2a Receptor- CCR2a Receptor
- Receptor, CCR2a
- MCP-1RA
- CCR-2A MCP-1 Receptor
- CCR 2A MCP 1 Receptor
- MCP-1 Receptor, CCR-2A
- Receptor, CCR-2A MCP-1
- MCP-1 Receptor CCR-2A
- MCP 1 Receptor CCR 2A
- Receptor CCR-2A, MCP-1
CCR2b Receptor- CCR2b Receptor
- Receptor, CCR2b
- MCP-1 Receptor 2B
- MCP 1 Receptor 2B
- CCR2b Receptors
- Receptors, CCR2b
- CC CKR2B
- MCP-1RB
|
Below are MeSH descriptors whose meaning is more general than "Receptors, CCR2".
- Chemicals and Drugs [D]
- Amino Acids, Peptides, and Proteins [D12]
- Proteins [D12.776]
- Membrane Proteins [D12.776.543]
- Receptors, Cell Surface [D12.776.543.750]
- Receptors, G-Protein-Coupled [D12.776.543.750.695]
- Receptors, Chemokine [D12.776.543.750.695.160]
- Receptors, CCR [D12.776.543.750.695.160.150]
- Receptors, CCR2 [D12.776.543.750.695.160.150.200]
- Receptors, Immunologic [D12.776.543.750.705]
- Receptors, Cytokine [D12.776.543.750.705.852]
- Receptors, Chemokine [D12.776.543.750.705.852.125]
- Receptors, CCR [D12.776.543.750.705.852.125.150]
- Receptors, CCR2 [D12.776.543.750.705.852.125.150.200]
Below are MeSH descriptors whose meaning is more specific than "Receptors, CCR2".
This graph shows the total number of publications written about "Receptors, CCR2" by people in this website by year, and whether "Receptors, CCR2" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 0 | 1 | 1 |
| 2017 | 2 | 1 | 3 |
| 2018 | 1 | 3 | 4 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Receptors, CCR2" by people in Profiles.
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Safety of inhaled ivermectin as a repurposed direct drug for treatment of COVID-19: A preclinical tolerance study. Int Immunopharmacol. 2021 Oct; 99:108004.
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CCR2 Regulates Vaccine-Induced Mucosal T-Cell Memory to Influenza A Virus. J Virol. 2021 07 12; 95(15):e0053021.
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Higher expression of monocyte chemotactic protein 1 in mild COVID-19 patients might be correlated with inhibition of Type I IFN signaling. Virol J. 2021 01 07; 18(1):12.
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Genetic mechanisms of critical illness in COVID-19. Nature. 2021 03; 591(7848):92-98.
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Found: genes that sway the course of the coronavirus. Science. 2020 10 16; 370(6514):275-276.
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The chemokine receptor antagonist cenicriviroc inhibits the replication of SARS-CoV-2 in vitro. Antiviral Res. 2020 10; 182:104902.
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Human ß-defensin 2 is involved in CCR2-mediated Nod2 signal transduction, leading to activation of the innate immune response in macrophages. Immunobiology. 2019 07; 224(4):502-510.
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Mechanical strain determines the site-specific localization of inflammation and tissue damage in arthritis. Nat Commun. 2018 11 05; 9(1):4613.
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The parasite-derived rOv-ASP-1 is an effective antigen-sparing CD4+ T cell-dependent adjuvant for the trivalent inactivated influenza vaccine, and functions in the absence of MyD88 pathway. Vaccine. 2018 06 14; 36(25):3650-3665.
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The atypical chemokine receptor ACKR2 drives pulmonary fibrosis by tuning influx of CCR2+ and CCR5+ IFN?-producing ?dT cells in mice. Am J Physiol Lung Cell Mol Physiol. 2018 06 01; 314(6):L1010-L1025.