Resumen
We have cloned a human cDNA for a novel CC chemokine receptor (CC CKR) designated CC CKR5 that has 48-75% amino acid identity to other CC CKRs. CC = CKR5 mRNA was detected constitutively in primary adherent monocytes but not in primary neutrophils or eosinophils. Macrophage inflammatory protein-1α (MIP-1α), MIP-1β, and RANTES were all potent agonists for CC CKR5 (EC50 = 3-30 nM) when calcium flux was measured in transfected HEK 293 cells, yet the apparent binding affinities of the corresponding iodinated chemokines to intact cells expressing the receptor were low (IC50 ~100 nM). The calcium flux responses were completely blocked by treatment of transfected cells with pertussis toxin. These data suggest that CC CKR5 is a G(i)-coupled receptor that may mediate monocyte responses to MIP-1α, MIP-1β, and RANTES.
| Idioma original | English (US) |
|---|---|
| Páginas (desde-hasta) | 147-152 |
| Número de páginas | 6 |
| Publicación | Journal of Leukocyte Biology |
| Volumen | 60 |
| N.º | 1 |
| DOI | |
| Estado | Published - jul 1996 |
ASJC Scopus subject areas
- Immunology and Allergy
- Cell Biology
- Immunology
Huella
Profundice en los temas de investigación de 'Cloning and functional expression of CC CKR5, a human monocytg CC chemokine receptor selective for MIP-1α, MIP-1β, and RANTES'. En conjunto forman una huella única.Citar esto
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