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Exosome-Mediated Ultra-Effective Direct Conversion of Human Fibroblasts into Neural Progenitor-like Cells

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dc.contributor.authorLee, Yong Seung-
dc.contributor.authorJung, Woon Yong-
dc.contributor.authorHeo, Hyejung-
dc.contributor.authorPark, Min Geun-
dc.contributor.authorOh, Seung-Hun-
dc.contributor.authorPark, Byong-Gon-
dc.contributor.authorKim, Soonhag-
dc.date.accessioned2022-07-12T07:34:07Z-
dc.date.available2022-07-12T07:34:07Z-
dc.date.created2021-05-14-
dc.date.issued2018-03-
dc.identifier.issn1936-0851-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/150354-
dc.description.abstractExosomes, naturally secreted nanoparticles, have been introduced as vehicles for horizontal transfer of genetic material. We induced autologous exosomes containing a cocktail of reprogramming factors ("reprosomes") to convert fibroblasts into neural progenitor cells (NPCs). The fibroblasts were treated with ultrasound and subsequently cultured in neural stem cell medium for 1 day to induce the release of reprosomes composed of reprogramming factors associated with chromatin remodeling and neural lineage-specific factors. After being treated with reprosomes, fibroblasts were converted into NPCs (rNPCs) with great efficiency via activation of chromatin remodeling, so quickly that only 5 days were required for the formation of 1500 spheroids showing an NPC-like phenotype. The rNPCs maintained self-renewal and proliferative properties for several weeks and successfully differentiated into neurons, astrocytes, and oligodendrocytes in vitro and in vivo. Reprosome-mediated cellular reprogramming is simple, safe, and efficient to produce autologous stem cells for clinical application.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleExosome-Mediated Ultra-Effective Direct Conversion of Human Fibroblasts into Neural Progenitor-like Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, Woon Yong-
dc.identifier.doi10.1021/acsnano.7b08297-
dc.identifier.scopusid2-s2.0-85044535276-
dc.identifier.wosid000428972600046-
dc.identifier.bibliographicCitationACS NANO, v.12, no.3, pp.2531 - 2538-
dc.relation.isPartOfACS NANO-
dc.citation.titleACS NANO-
dc.citation.volume12-
dc.citation.number3-
dc.citation.startPage2531-
dc.citation.endPage2538-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusHORIZONTAL TRANSFER-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusSOMATIC-CELLS-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordPlusMICROVESICLES-
dc.subject.keywordPlusMOUSE-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordAuthorultrasound-
dc.subject.keywordAuthorexosome-
dc.subject.keywordAuthorfibroblast-
dc.subject.keywordAuthorcellular reprogramming-
dc.subject.keywordAuthorchromatin remodeling-
dc.subject.keywordAuthorneural progenitor-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acsnano.7b08297-
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