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PMID: 8573157 Published · ppublish English Comparative Study Journal Article

Molecular cloning of murine CC CKR-4 and high affinity binding of chemokines to murine and human CC CKR-4.

Biochemical and biophysical research communications ·Vol. 218 ·No. 1 ·1996-01-05 ·Pages 337-43

Hoogewerf A, Black D, Proudfoot AE, Wells TN, Power CA

Abstract

We have cloned the murine homologue of human CC Chemokine Receptor-4 (CC CKR-4). In equilibrium competition binding assays performed in undifferentiated HL-60 cells transfected with human and murine CC CKR-4 cDNA, the IC50 values for the binding of [125I]macrophage inflammatory protein-1 alpha to human and murine CC CKR-4 were 14.5 +/- 9.0 nM and 10.1 +/- 3.0 nM, respectively, and the IC50 values for the binding of [125I]RANTES to human and murine CC CKR-4 were 9.3 +/- 3.0 nM and 5.7 +/- 2.6 nM, respectively. The cDNA clone for murine CC CKR-4 is 1531 bp, and the largest open reading frame encodes a protein of 360 amino acids that is 85% identical to human CC CKR-4. Murine CC CKR-4 was detected in the thymus and T-cell lines by Northern blot analysis. This first report of direct binding of chemokines to CC CKR-4 demonstrates that the highly homologous human and murine receptors have similar binding characteristics and tissue distribution.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Chemokine CCL4 Chemokine CCL5/metabolism Cloning, Molecular Gene Expression Gene Library HL-60 Cells Humans Kinetics Lymphocytes/metabolism Macrophage Inflammatory Proteins Mice Molecular Sequence Data Monokines/metabolism Organ Specificity RNA, Messenger/analysis,biosynthesis Receptors, Cytokine/biosynthesis,genetics,metabolism Recombinant Proteins/biosynthesis,metabolism Sequence Homology, Amino Acid Spleen/metabolism Substrate Specificity Thymus Gland/metabolism Transfection
Chemicals
CC cytokine receptor-4 Chemokine CCL4 Chemokine CCL5 Macrophage Inflammatory Proteins Monokines RNA, Messenger Receptors, Cytokine Recombinant Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hoogewerf A
Glaxo Institute for Molecular Biology, Geneva, Switzerland.
Black D
Proudfoot A E
Wells T N
Power C A
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1996-01-05
Pages
337-43
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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