Selective binding of the truncated form of the chemokine CK beta 8 (25-99)to CC chemokine receptor 1 (CCR1)

Citation
Ta. Berkhout et al., Selective binding of the truncated form of the chemokine CK beta 8 (25-99)to CC chemokine receptor 1 (CCR1), BIOCH PHARM, 59(5), 2000, pp. 591-596
Citations number
20
Categorie Soggetti
Pharmacology & Toxicology
Journal title
BIOCHEMICAL PHARMACOLOGY
ISSN journal
00062952 → ACNP
Volume
59
Issue
5
Year of publication
2000
Pages
591 - 596
Database
ISI
SICI code
0006-2952(20000301)59:5<591:SBOTTF>2.0.ZU;2-Q
Abstract
Human CC chemokine receptor 1 (CCR1) has been proposed as a receptor for CK beta 8. To obtain conclusive evidence, binding-displacement studies of I-1 25-CK beta 8 (25-99) were performed on membranes of Chinese hamster ovary c ells expressing human CCR1. The IC50 for displacement of I-125-CK beta 8 (2 5-99) with CK beta 8 (25-99) was 0.22 nM. The longer forms of CK beta 8 (24 -99 and 1-99) also displaced I-125-CK beta 8, with IC50 values of 6.5 and 1 6 nM, respectively. Displacement profiles of I-125-CK beta 8 (25-99) on fre shly prepared human monocytes indicated that CCR1 was the major receptor fo r CK beta 8. We conclude that CCR1 is a receptor for different-length CK be ta 8 and that CK beta 8 (25-99) has a similar affinity for CCR1 as macropha ge inflammatory protein-1 alpha (MIP-1 alpha). The longer variants CK beta 8 are significantly less potent than CK beta 8 (25-99) and MIP-1 alpha on C CR1 and monocytes (P < 0.05). (C) 2000 Elsevier Science Inc.