Direct reprogramming to human induced neuronal progenitors from fibroblasts of familial and sporadic Parkinson’s disease patients

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dc.contributor.authorMinhyung Lee-
dc.contributor.authorHyuna Sim-
dc.contributor.authorHyunjun Ahn-
dc.contributor.authorJeongmin Ha-
dc.contributor.authorAreum Baek-
dc.contributor.authorYoung Joo Jeon-
dc.contributor.authorMi Young Son-
dc.contributor.authorJanghwan Kim-
dc.date.accessioned2020-02-07T16:30:42Z-
dc.date.available2020-02-07T16:30:42Z-
dc.date.issued2019-
dc.identifier.issn2005-3606-
dc.identifier.uri10.15283/ijsc19075ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/19184-
dc.description.abstractIn Parkinson's disease (PD) research, human neuroblastoma and immortalized neural cell lines have been widely used as in vitro models. The advancement in the field of reprogramming technology has provided tools for generating patient-specific induced pluripotent stem cells (hiPSCs) as well as human induced neuronal progenitor cells (hiNPCs). These cells have revolutionized the field of disease modeling, especially in neural diseases. Although the direct reprogramming to hiNPCs has several advantages over differentiation after hiPSC reprogramming, such as the time required and the simple procedure, relatively few studies have utilized hiNPCs. Here, we optimized the protocol for hiNPC reprogramming using pluripotency factors and Sendai virus. In addition, we generated hiNPCs of two healthy donors, a sporadic PD patient, and a familial patient with the LRRK2 G2019S mutation (L2GS). The four hiNPC cell lines are highly proliferative, expressed NPC markers, maintained the normal karyotype, and have the differentiation potential of dopaminergic neurons. Importantly, the patient hiNPCs show different apoptotic marker expression. Thus, these hiNPCs, in addition to hiPSCs, are a favorable option to study PD pathology.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleDirect reprogramming to human induced neuronal progenitors from fibroblasts of familial and sporadic Parkinson’s disease patients-
dc.title.alternativeDirect reprogramming to human induced neuronal progenitors from fibroblasts of familial and sporadic Parkinson’s disease patients-
dc.typeArticle-
dc.citation.titleInternational Journal of Stem Cells-
dc.citation.number3-
dc.citation.endPage483-
dc.citation.startPage474-
dc.citation.volume12-
dc.contributor.affiliatedAuthorMinhyung Lee-
dc.contributor.affiliatedAuthorHyuna Sim-
dc.contributor.affiliatedAuthorHyunjun Ahn-
dc.contributor.affiliatedAuthorJeongmin Ha-
dc.contributor.affiliatedAuthorAreum Baek-
dc.contributor.affiliatedAuthorYoung Joo Jeon-
dc.contributor.affiliatedAuthorMi Young Son-
dc.contributor.affiliatedAuthorJanghwan Kim-
dc.contributor.alternativeName이민형-
dc.contributor.alternativeName심현아-
dc.contributor.alternativeName안현준-
dc.contributor.alternativeName하정민-
dc.contributor.alternativeName백아름-
dc.contributor.alternativeName전영주-
dc.contributor.alternativeName손미영-
dc.contributor.alternativeName김장환-
dc.identifier.bibliographicCitationInternational Journal of Stem Cells, vol. 12, no. 3, pp. 474-483-
dc.identifier.doi10.15283/ijsc19075-
dc.subject.keywordDirect reprogramming-
dc.subject.keywordInduced neuronal progenitor cells-
dc.subject.keywordParkinson's disease-
dc.subject.keywordPluripotency factors-
dc.subject.keywordReprogramming-
dc.subject.localDirect reprogramming-
dc.subject.localdirect reprogramming-
dc.subject.localInduced neuronal progenitor cells-
dc.subject.localParkinson disease-
dc.subject.localParkinson's disease-
dc.subject.localParkinson’s Disease-
dc.subject.localParkinson’s disease-
dc.subject.localParkinson’s diseases-
dc.subject.localParkinsons disease (PD)-
dc.subject.localParkinsons disease-
dc.subject.localParkinson's diasease-
dc.subject.localParkinson's Disease-
dc.subject.localPluripotency factors-
dc.subject.localReprogramming-
dc.subject.localreprogramming-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
Division of Biomedical Research > Disease Target Structure Research Center > 1. Journal Articles
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