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dc.contributor.authorWoo, CH-
dc.contributor.authorJeong, DT-
dc.contributor.authorYoon, SB-
dc.contributor.authorKim, KS-
dc.contributor.authorChung, IY-
dc.contributor.authorSaeki, T-
dc.contributor.authorKim, JH-
dc.date.accessioned2024-01-21T09:44:48Z-
dc.date.available2024-01-21T09:44:48Z-
dc.date.created2021-09-01-
dc.date.issued2002-11-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139105-
dc.description.abstractEotaxin 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.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleEotaxin induces migration of RBL-2H3 mast cells via a Rac-ERK-dependent pathway-
dc.typeArticle-
dc.identifier.doi10.1016/S0006-291X(02)02432-4-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.298, no.3, pp.392 - 397-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume298-
dc.citation.number3-
dc.citation.startPage392-
dc.citation.endPage397-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000179085100015-
dc.identifier.scopusid2-s2.0-0036429016-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.type.docTypeArticle-
dc.subject.keywordPlusHUMAN BASOPHILS-
dc.subject.keywordPlusRECEPTOR CCR3-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCHEMOKINE-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusCDC42-
dc.subject.keywordPlusEOSINOPHILS-
dc.subject.keywordPlusCHEMOTAXIS-
dc.subject.keywordPlusCLONING-
dc.subject.keywordAuthoreotaxin-
dc.subject.keywordAuthorchemotaxis-
dc.subject.keywordAuthorRBL-2H3-
dc.subject.keywordAuthorRac-
dc.subject.keywordAuthorERK-
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KIST Article > 2002
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