Abstract

The CC chemokine eotaxin is a selective chemoattractant for guinea pig eosinophils, first purified from bronchoalveolar lavage fluid in a guinea pig model of allergic airway inflammation. We have now isolated the gene and cDNA for a human counterpart of eotaxin. The gene maps to chromosome 17 and is expressed constitutively at high levels in small intestine and colon, and at lower levels in various other tissues. The deduced mature protein sequence is 66% identical to human monocyte chemoattractant protein-1, and 60% identical to guinea pig eotaxin. Recombinant human eotaxin produced in insect cells induced a calcium flux response in normal human eosinophils, but not in neutrophils or monocytes. The response could not be desensitized by pretreatment of eosinophils with other CC chemokines, suggesting a unique receptor. In this regard, we show that human eotaxin is a potent and highly specific agonist for CC chemokine receptor 3, a G protein-coupled receptor selectively expressed in human eosinophils. Thus eotaxin and CC chemokine receptor 3 may be host factors highly specialized for eosinophil recruitment in inflammation, and may be good targets for the development of selective drugs for inflammatory diseases where eosinophils contribute to pathogenesis, such as asthma.

Highlights

  • The CC chemokine eotaxin is a selective chemoattractant for guinea pig eosinophils, first purified from bronchoalveolar lavage fluid in a guinea pig model of allergic airway inflammation

  • We show that human eotaxin is a selective agonist for human eosinophils and for CC chemokine receptor 3 (CC CKR3), a 7-transmembrane-domain G protein-coupled receptor selectively expressed in eosinophils [14, 15]

  • While our data indicate high eosinophil selectivity for human eotaxin, more work will be needed to determine whether additional eotaxin functions exist and whether those established in the guinea pig have been conserved during mammalian evolution

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Summary

THE JOURNAL OF BIOLOGICAL CHEMISTRY

Vol 271, No 13, Issue of March 29, pp. 7725–7730, 1996 Printed in U.S.A. Molecular Cloning of Human Eotaxin, an Eosinophil-selective CC Chemokine, and Identification of a Specific Eosinophil Eotaxin Receptor, CC Chemokine Receptor 3*. The response could not be desensitized by pretreatment of eosinophils with other CC chemokines, suggesting a unique receptor In this regard, we show that human eotaxin is a potent and highly specific agonist for CC chemokine receptor 3, a G protein-coupled receptor selectively expressed in human eosinophils. Because of the pathologic potential of eosinophils, identification and pharmacologic control of the specific factors regulating their accumulation in vivo is an important goal In this regard, the CC chemokines macrophage inflammatory protein-1␣ (MIP-1␣), RANTES, and monocyte chemoattractant. We report the isolation of a cDNA and production of recombinant protein for a novel human CC chemokine named human eotaxin that is most closely related in sequence to human MCP-1 and guinea pig eotaxin. No other chemokines tested were agonists for CC CKR3, and eotaxin was not an agonist for the related receptors CC CKR1, CC CKR2B, and CC CKR52 (16 –18)

EXPERIMENTAL PROCEDURES
RESULTS
TABLE II CC chemokine receptor selectivity
DISCUSSION
Full Text
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