Hierarchy of eosinophil chemoattractants: role of p38 mitogen-activated protein kinase

✍ Scribed by Petra Schratl; Eva M. Sturm; Julia F. Royer; Gunter J. Sturm; Irmgard T. Lippe; Bernhard A. Peskar; Akos Heinemann

• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 359 KB
• Volume: 36
• Category: Article
• ISSN: 0014-2980
• DOI: 10.1002/eji.200535672

✦ Synopsis

Abstract

Several chemoattractants can regulate the recruitment of eosinophils to sites of inflammation, but the hierarchy among them is unknown. We observed here that eosinophil chemotaxis towards eotaxin or 5‐oxo‐6,8,11,14‐eicosatetraenoic acid (5‐oxo‐ETE) was amplified up to sixfold in the presence of prostaglandin (PG) D~2~. This effect was only seen in eosinophils, and not in neutrophils or basophils. Pretreatment with the chemoattractant receptor‐homologous molecule expressed on TH2 cells (CRTH2) antagonist ramatroban prevented the PGD~2~ enhancement of eosinophil migrations. In contrast, eotaxin or 5‐oxo‐ETE inhibited the migration of eosinophils towards PGD~2~. 5‐oxo‐ETE enhanced the chemotaxis to eotaxin, while eotaxin had no effect on 5‐oxo‐ETE‐induced migration. 5‐oxo‐ETE induced the phosphorylation of p38 mitogen‐activated protein kinase, and inhibition of p38 mitogen‐activated protein kinase by SB‐202190 converted the effect of 5‐oxo‐ETE on the chemotaxis to PGD~2~ from inhibition to enhancement. The presence of blood or plasma markedly decreased the sensitivity of eosinophils to eotaxin or 5‐oxo‐ETE, while responses to PGD~2~ were unaltered. In conclusion, PGD~2~ might be an initial chemoattractant, since it maintains its potency in the circulation and augments the responsiveness of eosinophils to other chemoattractants. In contrast, eotaxin seems to be an end‐point chemoattractant, since it has reduced efficacy in blood and is capable of down‐modulating eosinophil responsiveness to other chemoattractants.