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dc.contributor.authorBae, YS-
dc.contributor.authorPark, EY-
dc.contributor.authorLee, HY-
dc.contributor.authorKang, HK-
dc.contributor.authorSuh, PG-
dc.contributor.authorKwak, JY-
dc.contributor.authorRyu, SH-
dc.contributor.authorLee, T-
dc.date.accessioned2016-04-01T02:19:27Z-
dc.date.available2016-04-01T02:19:27Z-
dc.date.created2009-02-28-
dc.date.issued2004-12-10-
dc.identifier.issn0006-291X-
dc.identifier.other2004-OAK-0000004691-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/24914-
dc.description.abstractThe screening of small synthetic compound libraries is a useful means of identifying molecules that modulate various cellular responses. We screened more than 10,000 different small compounds and identified three synthetic compounds that stimulate arachidonic acid (AA) release in a combinational manner in neutrophil-like differentiated HL60 cells. These three compounds were designated as AARIC-1, -2, and -3, representing AA release inducing compounds-1, -2, and -3. Although AA release was not induced by any single one of these compounds, it was dramatically stimulated by the three compounds in combination. Moreover, the effect of combined treatment by these compounds on AA release was completely abolished by MAFP and AACOCF(3), specific cytosolic phospholipase A(2) inhibitors. Furthermore, we found that AARIC-3 stimulates cytosolic calcium influx, while AARIC-1 induces ERK activation. Taken together, we demonstrate a useful approach to the study of complicated and nonlinear intracellular signaling networks using small synthetic compounds in combination. (C) 2004 Elsevier Inc. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.subjectphospholipase A(2)-
dc.subjectsmall compound-
dc.subjectcombined treatment-
dc.subjectextracellular signal-regulated protein kinase-
dc.subjectcalcium influx-
dc.subjectARACHIDONIC-ACID RELEASE-
dc.subjectHUMAN MONOCYTES-
dc.subjectACTIVATION-
dc.subjectCELLS-
dc.subjectPHOSPHORYLATION-
dc.subjectGENERATION-
dc.subjectIDENTIFICATION-
dc.subjectNEUTROPHILS-
dc.subjectEXPRESSION-
dc.subjectRECEPTORS-
dc.titleCompounds stimulating cytosolic phospholipase A(2) activity with a combinational action mode-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1016/j.bbrc.2004.10.063-
dc.author.googleBae, YS-
dc.author.googlePark, EY-
dc.author.googleLee, HY-
dc.author.googleKang, HK-
dc.author.googleSuh, PG-
dc.author.googleKwak, JY-
dc.author.googleRyu, SH-
dc.author.googleLee, T-
dc.relation.volume325-
dc.relation.issue2-
dc.relation.startpage632-
dc.relation.lastpage638-
dc.contributor.id10052640-
dc.relation.journalBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.325, no.2, pp.632 - 638-
dc.identifier.wosid000225279600039-
dc.date.tcdate2018-03-23-
dc.citation.endPage638-
dc.citation.number2-
dc.citation.startPage632-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume325-
dc.contributor.affiliatedAuthorSuh, PG-
dc.contributor.affiliatedAuthorRyu, SH-
dc.identifier.scopusid2-s2.0-7644224240-
dc.description.journalClass1-
dc.description.journalClass1-
dc.type.docTypeArticle-
dc.subject.keywordPlusARACHIDONIC-ACID RELEASE-
dc.subject.keywordPlusHUMAN MONOCYTES-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusNEUTROPHILS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusRECEPTORS-
dc.subject.keywordAuthorphospholipase A(2)-
dc.subject.keywordAuthorsmall compound-
dc.subject.keywordAuthorcombined treatment-
dc.subject.keywordAuthorextracellular signal-regulated protein kinase-
dc.subject.keywordAuthorcalcium influx-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-

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류성호RYU, SUNG HO
Dept of Life Sciences
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