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Rat mesenchymal stem cells increase tyrosine hydroxylase expression and dopamine content in ventral mesencephalic cells in vitro

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dc.contributor.authorJin, Guang-Zhen-
dc.contributor.authorCho, Su-Jin-
dc.contributor.authorChoi, Eu-Gene-
dc.contributor.authorLee, Young-S.-
dc.contributor.authorYu, Xian-Feng-
dc.contributor.authorChoi, Kap-Seong-
dc.contributor.authorYee, Sung-Tae-
dc.contributor.authorJeon, Jin-Tae-
dc.contributor.authorKim, Myeong-Ok-
dc.contributor.authorKong, Il-Keun-
dc.date.accessioned2022-12-27T06:03:08Z-
dc.date.available2022-12-27T06:03:08Z-
dc.date.issued2008-11-
dc.identifier.issn1065-6995-
dc.identifier.issn1095-8355-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/27230-
dc.description.abstractMesenchymal stem cells (MSCs) are pluripotent adult stem cells. It has been shown that MSCs secrete neurotrophic factors involving nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF). Also, these neurotrophic factors can upregulate tyrosine hydroxylase (TH) gene expression in PC12 cells and neural stem cells. Here, we investigated the effect of co-culturing rat E13.5 ventral mesencephalic cells (VMCs) with MSCs from rat bone marrow on TH expression and dopamine (DA) content. The study consisted of 3 groups: MSC, VMC and a combined MSC + VMC group. All groups were cultured in serum-free neuro-basal medium for 3 days. Thereafter, each group was analyzed by RT-PCR, western blotting, and HPLC. The co-culture group showed a higher expression at TH and DA than the VMC group. However, TH and DA were not present in the MSC group. These observations suggest that MSCs could be an alternative source for treating neurodegenerative diseases such as Parkinson's disease (PD). Crown Copyright (C) 2008 Published by Elsevier Ltd on behalf of International Federation for Cell Biology. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherPORTLAND PRESS LTD-
dc.titleRat mesenchymal stem cells increase tyrosine hydroxylase expression and dopamine content in ventral mesencephalic cells in vitro-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.cellbi.2008.08.014-
dc.identifier.scopusid2-s2.0-54049086053-
dc.identifier.wosid000260671900012-
dc.identifier.bibliographicCitationCELL BIOLOGY INTERNATIONAL, v.32, no.11, pp 1433 - 1438-
dc.citation.titleCELL BIOLOGY INTERNATIONAL-
dc.citation.volume32-
dc.citation.number11-
dc.citation.startPage1433-
dc.citation.endPage1438-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusMARROW STROMAL CELLS-
dc.subject.keywordPlusNERVE GROWTH-FACTOR-
dc.subject.keywordPlusTRAUMATIC BRAIN-INJURY-
dc.subject.keywordPlusPARKINSONS-DISEASE-
dc.subject.keywordPlusFUNCTIONAL RECOVERY-
dc.subject.keywordPlusPC12 CELLS-
dc.subject.keywordPlusBONE-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusTRANSPLANTATION-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordAuthorCo-culture-
dc.subject.keywordAuthorDopamine-
dc.subject.keywordAuthorMesenchymal stem cells-
dc.subject.keywordAuthorTyrosine hydroxylase-
dc.subject.keywordAuthorVentral mesencephalic cells-
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