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Methylmercury induces caspase-dependent apoptosis and autophagy in human neural stem cells

DC Field Value Language
dc.contributor.authorChang, Seung-Hee-
dc.contributor.authorLee, Hong Jun-
dc.contributor.authorKang, Bitna-
dc.contributor.authorYu, Kyeong-Nam-
dc.contributor.authorMinai-Tehrani, Arash-
dc.contributor.authorLee, Somin-
dc.contributor.authorKim, Seung U.-
dc.contributor.authorCho, Myung-Haing-
dc.date.accessioned2021-01-31T08:46:42Z-
dc.date.available2021-01-31T08:46:42Z-
dc.date.created2020-12-10-
dc.date.issued2013-12-
dc.identifier.citationJournal of Toxicological Sciences, Vol.38 No.6, pp.823-831-
dc.identifier.issn0388-1350-
dc.identifier.other118954-
dc.identifier.urihttps://hdl.handle.net/10371/172447-
dc.description.abstractMethylmercury (MeHg) is a well-known human neurotoxic agent whose exposure sources are mainly environmental and aquatic-derived food. MeHg is reported to induce central nervous system disability. However, the exact mechanism of MeHg-induced neurotoxicity is still unknown. In this study, to investigate which cell death signaling pathway is related with MeHg-induced cytotoxicity, the effects of MeHg on apoptosis and autophagy were evaluated in HB1.F3 human neural stem cells (NSCs). Human NSCs were treated with 1 mu M of MeHg for 48 hr and the effect of MeHg on cell signaling pathway was elucidated. MeHg inhibited Akt1/mTOR signaling that led to induction of caspase-dependent apoptosis and autophagy in the NSCs. Furthermore, retinoic acid (RA)-induced neuronal differentiation was inhibited by MeHg. Taken together, these results suggest that MeHg inhibits the differentiation of human NSCs by induction of caspase-dependent apoptosis and autophagy.-
dc.language영어-
dc.publisherJapanese Society of Toxicological Sciences-
dc.titleMethylmercury induces caspase-dependent apoptosis and autophagy in human neural stem cells-
dc.typeArticle-
dc.contributor.AlternativeAuthor조명행-
dc.citation.journaltitleJournal of Toxicological Sciences-
dc.identifier.wosid000328008100003-
dc.identifier.scopusid2-s2.0-84887427376-
dc.citation.endpage831-
dc.citation.number6-
dc.citation.startpage823-
dc.citation.volume38-
dc.identifier.sci000328008100003-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorCho, Myung-Haing-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusACTIN-
dc.subject.keywordPlusNEUROTOXICITY-
dc.subject.keywordPlusNECROSIS-
dc.subject.keywordPlusPOLARITY-
dc.subject.keywordPlusMERCURY-
dc.subject.keywordPlusSIGNALS-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusCYTOSKELETON-
dc.subject.keywordAuthorMethylmercury (MeHg)-
dc.subject.keywordAuthorHuman neural stem cell (NSC)-
dc.subject.keywordAuthorApoptosis-
dc.subject.keywordAuthorAutophagy-
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  • Department of Veterinary Medicine
Research Area Nanotoxicology, Veterinary Toxicology

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