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Platelet‐activating factor drives eotaxin production in an allergic pleurisy in mice
Author(s) -
Klein André,
Pinho Vanessa,
Alessandrini Ana Letícia,
Shimizu Takao,
Ishii Satoshi,
Teixeira Mauro M
Publication year - 2002
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0704570
Subject(s) - eotaxin , eosinophil , platelet activating factor , pleurisy , receptor , immunology , pharmacology , stimulation , eosinophil cationic protein , receptor antagonist , medicine , chemistry , antagonist , endocrinology , asthma , pleural effusion
The activation of eosinophils via G‐protein‐coupled seven transmembran receptors play a necessary role in the recruitment of these cells into tissue. The present study investigates a role for PAF in driving eotaxin production and eosinophil recruitment in an allergic pleurisy model in mice. The intrapleural injection of increasing doses of PAF (10 −11 to 10 −9 moles per cavity) induced a dose‐ and PAF receptor‐dependent recruitment of eosinophils 48 h after stimulation. Intrapleural injection of PAF induced the rapid (within 1 h) release of eotaxin into the pleural cavity of mice and an anti‐eotaxin antibody effectively inhibited PAF‐induced recruitment of eosinophils. Eosinophil recruitment in the allergic pleurisy was markedly inhibited by the PAF receptor antagonist UK‐74,505 (modipafant, 1 mg kg −1 ). Moreover, recruitment of eosinophils in sensitized and challenged PAF receptor‐deficient animals was lower than that observed in wild‐type animals. Blockade of PAF receptors with UK‐74,505 suppressed by 85% the release of eotaxin in the allergic pleurisy. Finally, the injection of a sub‐threshold dose of PAF and eotaxin cooperated to induce eosinophil recruitment in vivo . In conclusion, the production of PAF in an allergic reaction could function in multiple ways to facilitate the recruitment of eosinophils  –  by facilitating eotaxin release and by cooperating with eotaxin to induce greater recruitment of eosinophils.British Journal of Pharmacology (2002) 135 , 1213–1218; doi: 10.1038/sj.bjp.0704570

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