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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Cytokine
Article . 2000 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
Cytokine
Article . 2000
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IDENTIFICATION OF A COMMON RECEPTOR FOR THREE TYPES OF RAT CYTOKINE-INDUCED NEUTROPHIL CHEMOATTRACTANTS (CINCS)

Authors: Futoshi Shibata; Hideo Nakagawa; Kiyoshi Konishi;

IDENTIFICATION OF A COMMON RECEPTOR FOR THREE TYPES OF RAT CYTOKINE-INDUCED NEUTROPHIL CHEMOATTRACTANTS (CINCS)

Abstract

Rat cytokine-induced neutrophil chemoattractant-1 (CINC-1), CINC-2 and CINC-3/macrophage inflammatory protein-2 (MIP-2), members of the CXC chemokine family, are potent chemotactic factors for neutrophils. In order to identify the receptor for CINCs, rat CXC chemokine receptor 2 (CXCR2) was cloned and expressed in HEK293 cells. CINC-1, CINC-2 and CINC-3 induced calcium mobilizations dose-dependently in CXCR2-transfected cells, whereas formyl-methionyl-leucyl-phenylalanine (FMLP) did not. CINC-3 induced enhancement of cytoplasmic calcium concentration more potently than CINC-1 and CINC-2, and desensitized calcium transients induced by CINC-1 and CINC-2, which were essentially identical to those observed in rat neutrophils. In addition, anti-CXCR2 serum inhibited neutrophil chemotactic activities of three types of CINCs almost completely. The mutant CINC-3, whose amino-terminal amino acid sequence (SELR) was replaced to AAR, lost chemotactic activity of its own but inhibited that of CINC-1 and CINC-2 potently, and that of CINC-3 weakly. The results indicate that rat CXCR2 on neutrophils is the unique receptor for all three types of CINCs, and CINC-1/-2 and CINC-3 exert different biological activities through the common receptor.

Keywords

DNA, Complementary, Chemotactic Factors, Dose-Response Relationship, Drug, Neutrophils, Chemokine CXCL1, Chemotaxis, Chemokine CXCL2, Blotting, Northern, Cell Line, N-Formylmethionine Leucyl-Phenylalanine, Liver, Mutagenesis, Animals, Humans, Intercellular Signaling Peptides and Proteins, Calcium, Electrophoresis, Polyacrylamide Gel, Cloning, Molecular, Growth Substances, Chemokines, CXC

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
53
Top 10%
Top 10%
Top 10%