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dc.contributor.authorLee, CH-
dc.contributor.authorLee, MS-
dc.contributor.authorKim, SJ-
dc.contributor.authorJe, YT-
dc.contributor.authorRyu, SH-
dc.contributor.authorLee, T-
dc.date.accessioned2016-04-01T08:47:10Z-
dc.date.available2016-04-01T08:47:10Z-
dc.date.created2009-07-30-
dc.date.issued2009-02-
dc.identifier.issn0196-9781-
dc.identifier.other2009-OAK-0000017060-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/28762-
dc.description.abstractA novel synthetic hexapeptide (SFKLRY-NH2) that displays angiogenic activity has been identified by positional scanning of a synthetic peptide combinatorial library (PS-SPCL). The peptide induced proliferation, migration, and capillary-like tube formation in primary cultured HUVECs, and augmented vessel sprouting ex vivo while attenuated by the treatment with per-tussis toxin (PTX) or U73122 (PLC-inhibitor) suggesting the influence of PTX-sensitive G-proteins and PLC. In addition, SFKLRY-NH2 up-regulated the expression of VEGF-A in HUVECs and the neutralizing antibody against VEGF suppressed SFKLRY-NH2-induced tube formation activity. Taken together, these results suggest that SFKLRY-NH2 may induce blood vessel formation by PTX-sensitive G protein-coupled receptor-PLC-Ca2+ signaling cascade leading into VEGF-A expression in HUVECs. (C) 2008 Elsevier Inc. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE INC-
dc.relation.isPartOfPEPTIDES-
dc.subjectSFKLRY-NH(2)-
dc.subjectGPCR-
dc.subjectCalcium-
dc.subjectVEGF-
dc.subjectHUVECs-
dc.subjectAngiogenesis-
dc.subjectPS-SPCL-
dc.subjectGROWTH-FACTOR-
dc.subjectINOSITOL TRISPHOSPHATE-
dc.subjectSIGNAL-TRANSDUCTION-
dc.subjectHYDROLYSIS-
dc.subjectACTIVATION-
dc.subjectMASTOPARAN-
dc.subjectCALCIUM-
dc.subjectKINASE-
dc.subjectMECHANISMS-
dc.subjectGENERATION-
dc.titleIdentification of novel synthetic peptide showing angiogenic activity in human endothelial cells-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1016/j.peptides.2008.10.003-
dc.author.googleLee, CH-
dc.author.googleLee, MS-
dc.author.googleKim, SJ-
dc.author.googleJe, YT-
dc.author.googleRyu, SH-
dc.author.googleLee, T-
dc.relation.volume30-
dc.relation.issue2-
dc.relation.startpage409-
dc.relation.lastpage418-
dc.contributor.id10069853-
dc.relation.journalPEPTIDES-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationPEPTIDES, v.30, no.2, pp.409 - 418-
dc.identifier.wosid000263447700027-
dc.date.tcdate2019-02-01-
dc.citation.endPage418-
dc.citation.number2-
dc.citation.startPage409-
dc.citation.titlePEPTIDES-
dc.citation.volume30-
dc.contributor.affiliatedAuthorRyu, SH-
dc.identifier.scopusid2-s2.0-58149479560-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc4-
dc.type.docTypeArticle-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusINOSITOL TRISPHOSPHATE-
dc.subject.keywordPlusSIGNAL-TRANSDUCTION-
dc.subject.keywordPlusHYDROLYSIS-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusMASTOPARAN-
dc.subject.keywordPlusCALCIUM-
dc.subject.keywordPlusKINASE-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordAuthorSFKLRY-NH2-
dc.subject.keywordAuthorGPCR-
dc.subject.keywordAuthorCalcium-
dc.subject.keywordAuthorVEGF-
dc.subject.keywordAuthorHUVECs-
dc.subject.keywordAuthorAngiogenesis-
dc.subject.keywordAuthorPS-SPCL-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryEndocrinology & Metabolism-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaEndocrinology & Metabolism-
dc.relation.journalResearchAreaPharmacology & Pharmacy-

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Dept of Life Sciences
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