Eotaxin induces migration of RBL-2H3 mast cells via a Rac-ERK-dependent pathway

Authors
Woo, CHJeong, DTYoon, SBKim, KSChung, IYSaeki, TKim, JH
Issue Date
2002-11
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.298, no.3, pp.392 - 397
Abstract
Eotaxin is a potent chemokine that acts via CC chemokine receptor 3 (CCR3) to induce chemotaxis, mainly on eosinophils. Here we show that eotaxin also induces chemotactic migration in rat basophilic leukemia (RBL-2H3) mast cells. This effect was dose-dependently inhibited by compound X, a selective CCR3 antagonist, indicating that, as in eosinophils, the effect was mediated by CCR3. Eotaxin-induced cell migration was completely blocked in RBL-RacN17 cells expressing a dominant negative Racl mutant, suggesting a crucial role for Racl in eotaxin signaling to chemotactic migration. ERK activation also proved essential for eotaxin signaling and it too was absent in RBL-RacN17 cells. Finally, we found that activation of Rac and ERK was correlated with eotaxin-induced actin reorganization known to be necessary for cell motility. It thus appears that Racl acts upstream of ERK to signal chemotaxis in these cells, and that a Rac-ERK-dependent cascade mediates the eotaxin-induced chemotactic motility of RBL-2H3 mast cells. (C) 2002 Elsevier Science (USA). All rights reserved.
Keywords
HUMAN BASOPHILS; RECEPTOR CCR3; ACTIVATION; EXPRESSION; CHEMOKINE; IDENTIFICATION; CDC42; EOSINOPHILS; CHEMOTAXIS; CLONING; eotaxin; chemotaxis; RBL-2H3; Rac; ERK
ISSN
0006-291X
URI
https://pubs.kist.re.kr/handle/201004/139105
DOI
10.1016/S0006-291X(02)02432-4
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KIST Article > 2002
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