Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, Youn-Jung | - |
dc.contributor.author | Kim, Young-Seok | - |
dc.contributor.author | Kim, Mi-Soon | - |
dc.contributor.author | Ryu, Jae-Chun | - |
dc.date.accessioned | 2024-01-21T01:02:57Z | - |
dc.date.available | 2024-01-21T01:02:57Z | - |
dc.date.created | 2021-09-02 | - |
dc.date.issued | 2007-05-05 | - |
dc.identifier.issn | 0300-483X | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/134398 | - |
dc.description.abstract | Methylmercury (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.language | English | - |
dc.publisher | ELSEVIER IRELAND LTD | - |
dc.subject | PROTEIN-KINASE-C | - |
dc.subject | NEURITE OUTGROWTH | - |
dc.subject | MAP KINASE | - |
dc.subject | RETINOIC ACID | - |
dc.subject | SUSTAINED ACTIVATION | - |
dc.subject | NERVOUS-SYSTEM | - |
dc.subject | GROWTH-FACTOR | - |
dc.subject | HEAVY-METALS | - |
dc.subject | PC12 CELLS | - |
dc.subject | IN-VITRO | - |
dc.title | The inhibitory mechanism of methylmercury on differentiation of human neuroblastorna cells | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.tox.2007.01.003 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | TOXICOLOGY, v.234, no.1-2, pp.1 - 9 | - |
dc.citation.title | TOXICOLOGY | - |
dc.citation.volume | 234 | - |
dc.citation.number | 1-2 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 9 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000246275800001 | - |
dc.identifier.scopusid | 2-s2.0-34047132151 | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Toxicology | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Toxicology | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | PROTEIN-KINASE-C | - |
dc.subject.keywordPlus | NEURITE OUTGROWTH | - |
dc.subject.keywordPlus | MAP KINASE | - |
dc.subject.keywordPlus | RETINOIC ACID | - |
dc.subject.keywordPlus | SUSTAINED ACTIVATION | - |
dc.subject.keywordPlus | NERVOUS-SYSTEM | - |
dc.subject.keywordPlus | GROWTH-FACTOR | - |
dc.subject.keywordPlus | HEAVY-METALS | - |
dc.subject.keywordPlus | PC12 CELLS | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordAuthor | methylmercury | - |
dc.subject.keywordAuthor | differentiation | - |
dc.subject.keywordAuthor | cell cycle | - |
dc.subject.keywordAuthor | retinoic acid | - |
dc.subject.keywordAuthor | ERK | - |
dc.subject.keywordAuthor | PKC | - |
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