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CK beta 8/CCL23 and its isoform CK beta 8-1 induce up-regulation of cyclins via the G(i)/G(o) protein/PLC/PKC delta/ERK leading to cell-cycle progression

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dc.contributor.authorKim, Jeonghan-
dc.contributor.authorKim, Yoon Suk-
dc.contributor.authorKo, Jesang-
dc.date.accessioned2021-09-08T04:05:49Z-
dc.date.available2021-09-08T04:05:49Z-
dc.date.created2021-06-11-
dc.date.issued2010-04-
dc.identifier.issn1043-4666-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/116687-
dc.description.abstractCK beta 8/CCL23 is a CC chemokine and alternative splicing of the CK beta 8 gene produces two mRNAs that encode CK beta 8 and its isoform CK beta 8-1. Chemokines play a critical role in leukocyte trafficking and development of inflammation and chemokines are also known to be involved in cell proliferation. To investigate participation of CK beta 8 and CK beta 8-1 in cell proliferation, we examined the effects of CK beta 8 and CK beta 8-1 in the cell cycle. Both CK beta 8 and CK beta 8-1 induced cell-cycle progression. We next investigated whether MAPKs are involved in CK beta 8- and CK beta 8-1-induced cell proliferation. CK beta 8- and CK beta 8-1-stimulated cells showed phosphorylation of ERK1/2 and an inhibitor study indicated that CK beta 8- and CK beta 8-1-induced activation of ERK1/2 is mediated by the G(i)/G(o) protein, PLC, and PKC delta. CK beta 8 and CK beta 8-1 regulated expression of the cell cycle regulators cyclin D-3 and cyclin B-1, and the immediate early response gene products c-Myc and Egr-1. These results indicate that both CK beta 8 and CK beta 8-1 are involved in cell proliferation by modulating the cell cycle regulators. (C) 2009 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD-
dc.subjectCHEMOKINE RECEPTORS-
dc.subjectCC-CHEMOKINE-
dc.subjectPROLIFERATION-
dc.subjectINHIBITORS-
dc.subjectSPECIFICITY-
dc.titleCK beta 8/CCL23 and its isoform CK beta 8-1 induce up-regulation of cyclins via the G(i)/G(o) protein/PLC/PKC delta/ERK leading to cell-cycle progression-
dc.typeArticle-
dc.contributor.affiliatedAuthorKo, Jesang-
dc.identifier.doi10.1016/j.cyto.2009.12.010-
dc.identifier.scopusid2-s2.0-77049085215-
dc.identifier.wosid000275986100007-
dc.identifier.bibliographicCitationCYTOKINE, v.50, no.1, pp.42 - 49-
dc.relation.isPartOfCYTOKINE-
dc.citation.titleCYTOKINE-
dc.citation.volume50-
dc.citation.number1-
dc.citation.startPage42-
dc.citation.endPage49-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusCHEMOKINE RECEPTORS-
dc.subject.keywordPlusCC-CHEMOKINE-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusSPECIFICITY-
dc.subject.keywordAuthorCK beta 8-
dc.subject.keywordAuthorCK beta 8-1-
dc.subject.keywordAuthorCell cycle-
dc.subject.keywordAuthorCyclin-
dc.subject.keywordAuthorSignal transduction-
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