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dc.contributor.authorKim, Youn-Jung-
dc.contributor.authorKim, Young-Seok-
dc.contributor.authorKim, Mi-Soon-
dc.contributor.authorRyu, Jae-Chun-
dc.date.accessioned2024-01-21T01:02:57Z-
dc.date.available2024-01-21T01:02:57Z-
dc.date.created2021-09-02-
dc.date.issued2007-05-05-
dc.identifier.issn0300-483X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/134398-
dc.description.abstractMethylmercury (MeHg) is a ubiquitous environmental toxicant and shows neurotoxicity to central nerve system (CNS) or neuronal cells. It has been known that MeHg has more influence to developing or differentiating CNS/neuronal cells than adult or differentiated CNS/neuronal cells. This study examined the effect of MeHg on differentiation of human neuroblastoma SH-SY5Y cells induced by all-trans-retinoic acid (RA). MeHg caused the impairment of the RA-induced G(1/0) phase arrest; it was induced the reduction of G(1/0) phase and S phase arrest. Extracellular signal-regulated kinase 1/2 (ERK1/2) and protein kinase C (PKC) are involved in the RA-mediated differentiation and cell cycle progression. Activation of ERK1/2 by RA was increased more in MeHg-treated differentiating cells, comparing with only RA-treated groups. Furthermore, in both cases of inhibition of ERK1/2 with PD98059 or inhibition of PKC with GF109203X, RA/MeHg-induced ERK1/2 phosphorylation was reduced and G(1/0) phase arrest was induced. Thus, it indicates that the neuronal differentiation with RA was mediated by the ERK1/2 and PKC related pathway and MeHg resulted in neurotoxic influences through the disturbance in steps of differentiation by this pathway. These results suggest that MeHg inhibits RA-induced differentiation in SH-SY5Y cells by a pathway dependent ERK1/2 and PKC. (C) 2007 Elsevier Ireland Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectPROTEIN-KINASE-C-
dc.subjectNEURITE OUTGROWTH-
dc.subjectMAP KINASE-
dc.subjectRETINOIC ACID-
dc.subjectSUSTAINED ACTIVATION-
dc.subjectNERVOUS-SYSTEM-
dc.subjectGROWTH-FACTOR-
dc.subjectHEAVY-METALS-
dc.subjectPC12 CELLS-
dc.subjectIN-VITRO-
dc.titleThe inhibitory mechanism of methylmercury on differentiation of human neuroblastorna cells-
dc.typeArticle-
dc.identifier.doi10.1016/j.tox.2007.01.003-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTOXICOLOGY, v.234, no.1-2, pp.1 - 9-
dc.citation.titleTOXICOLOGY-
dc.citation.volume234-
dc.citation.number1-2-
dc.citation.startPage1-
dc.citation.endPage9-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000246275800001-
dc.identifier.scopusid2-s2.0-34047132151-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaToxicology-
dc.type.docTypeArticle-
dc.subject.keywordPlusPROTEIN-KINASE-C-
dc.subject.keywordPlusNEURITE OUTGROWTH-
dc.subject.keywordPlusMAP KINASE-
dc.subject.keywordPlusRETINOIC ACID-
dc.subject.keywordPlusSUSTAINED ACTIVATION-
dc.subject.keywordPlusNERVOUS-SYSTEM-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusHEAVY-METALS-
dc.subject.keywordPlusPC12 CELLS-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordAuthormethylmercury-
dc.subject.keywordAuthordifferentiation-
dc.subject.keywordAuthorcell cycle-
dc.subject.keywordAuthorretinoic acid-
dc.subject.keywordAuthorERK-
dc.subject.keywordAuthorPKC-
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