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Endothelin 1 protects HN33 cells from serum deprivation-induced neuronal apoptosis through Ca2+-PKC alpha-ERK pathway

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dc.contributor.authorPark, Moon Ho-
dc.contributor.authorLee, Dae Hie-
dc.date.accessioned2021-09-09T10:59:25Z-
dc.date.available2021-09-09T10:59:25Z-
dc.date.created2021-06-10-
dc.date.issued2008-02-29-
dc.identifier.issn1226-3613-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/124051-
dc.description.abstractEndothelins (ETs), which were originally found to be potent vasoactive transmitters, were known to be implicated in nervous system, but the mode of mechanism remains unclear. ETs (ET-1, ET-2, and ET-3) were added to HN33 (mouse hippocampal neuron X neuroblastoma) cells. Among the three types of ET, only ET-1 increased the intracellular calcium levels in a PLC. dependent manner with the induction of ERK 1/2 activation. As the result of ET-1 exposure, the survival rate of HN33 cells and the PKC alpha. translocation into the plasma membrane were increased. We suggest that ET-1 participated in the neuroprotective effect involving the calcium-PKC alpha-ERK1/2 pathway.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherNATURE PUBLISHING GROUP-
dc.subjectRAT-BRAIN-
dc.subjectSUBSTRATE MARCKS-
dc.subjectNERVOUS-SYSTEM-
dc.subjectKINASE-C-
dc.subjectRECEPTOR-
dc.subjectHIPPOCAMPUS-
dc.subjectEXPRESSION-
dc.subjectSURVIVAL-
dc.subjectPEPTIDE-
dc.subjectCLONING-
dc.titleEndothelin 1 protects HN33 cells from serum deprivation-induced neuronal apoptosis through Ca2+-PKC alpha-ERK pathway-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Moon Ho-
dc.contributor.affiliatedAuthorLee, Dae Hie-
dc.identifier.doi10.3858/emm.2008.40.1.92-
dc.identifier.scopusid2-s2.0-40449120485-
dc.identifier.wosid000253876400011-
dc.identifier.bibliographicCitationEXPERIMENTAL AND MOLECULAR MEDICINE, v.40, no.1, pp.92 - 97-
dc.relation.isPartOfEXPERIMENTAL AND MOLECULAR MEDICINE-
dc.citation.titleEXPERIMENTAL AND MOLECULAR MEDICINE-
dc.citation.volume40-
dc.citation.number1-
dc.citation.startPage92-
dc.citation.endPage97-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001246452-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordPlusRAT-BRAIN-
dc.subject.keywordPlusSUBSTRATE MARCKS-
dc.subject.keywordPlusNERVOUS-SYSTEM-
dc.subject.keywordPlusKINASE-C-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusHIPPOCAMPUS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusCLONING-
dc.subject.keywordAuthorcalcium-
dc.subject.keywordAuthorcell survival-
dc.subject.keywordAuthorendothelins-
dc.subject.keywordAuthormitogen-activated protein kinase 1-
dc.subject.keywordAuthorneurons-
dc.subject.keywordAuthorprotein kinase C-
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