Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Woo, CH | - |
dc.contributor.author | Jeong, DT | - |
dc.contributor.author | Yoon, SB | - |
dc.contributor.author | Kim, KS | - |
dc.contributor.author | Chung, IY | - |
dc.contributor.author | Saeki, T | - |
dc.contributor.author | Kim, JH | - |
dc.date.accessioned | 2024-01-21T09:44:48Z | - |
dc.date.available | 2024-01-21T09:44:48Z | - |
dc.date.created | 2021-09-01 | - |
dc.date.issued | 2002-11 | - |
dc.identifier.issn | 0006-291X | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/139105 | - |
dc.description.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. | - |
dc.language | English | - |
dc.publisher | ACADEMIC PRESS INC ELSEVIER SCIENCE | - |
dc.title | Eotaxin induces migration of RBL-2H3 mast cells via a Rac-ERK-dependent pathway | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/S0006-291X(02)02432-4 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.298, no.3, pp.392 - 397 | - |
dc.citation.title | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
dc.citation.volume | 298 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 392 | - |
dc.citation.endPage | 397 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000179085100015 | - |
dc.identifier.scopusid | 2-s2.0-0036429016 | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Biophysics | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Biophysics | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | HUMAN BASOPHILS | - |
dc.subject.keywordPlus | RECEPTOR CCR3 | - |
dc.subject.keywordPlus | ACTIVATION | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | CHEMOKINE | - |
dc.subject.keywordPlus | IDENTIFICATION | - |
dc.subject.keywordPlus | CDC42 | - |
dc.subject.keywordPlus | EOSINOPHILS | - |
dc.subject.keywordPlus | CHEMOTAXIS | - |
dc.subject.keywordPlus | CLONING | - |
dc.subject.keywordAuthor | eotaxin | - |
dc.subject.keywordAuthor | chemotaxis | - |
dc.subject.keywordAuthor | RBL-2H3 | - |
dc.subject.keywordAuthor | Rac | - |
dc.subject.keywordAuthor | ERK | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.