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Uniform-sized neurosphere-mediated motoneuron differentiation in microwell arrays

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dc.contributor.authorLee, Jong Min-
dc.contributor.authorMoon, Joo Yoon-
dc.contributor.authorShaker, Mohammed R.-
dc.contributor.authorSun, Woong-
dc.contributor.authorChung, Bong Geun-
dc.date.accessioned2021-09-02T22:11:27Z-
dc.date.available2021-09-02T22:11:27Z-
dc.date.created2021-06-16-
dc.date.issued2017-12-
dc.identifier.issn0173-0835-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/81260-
dc.description.abstractWe developed the photocrosslinkable hydrogel microwell arrays for uniform-sized neurosphere-mediated motoneuron differentiation. Neural stem cells (NSCs) were obtained from embryonic cerebral cortex and spinal cord. To generate uniform-sized neurospheres in a homogeneous manner, the dissociated cells were cultured in the hydrogel microwell arrays for 3 days. Uniform-sized neurospheres harvested from microwell arrays were replated into laminin-coated substrate. In parallel, uniform-sized neurospheres cultured in microwell arrays were encapsulated by photocrosslinkable gelatin methacrylate hydrogels in a three-dimensional manner. We demonstrated the effect of hydrogel microwell sizes (e.g., 50, 100, 150m in diameter) on motoneuron differentiation, showing that the largest uniform-sized neurospheres derived from embryonic spinal cord efficiently differentiated into motoneurons. Therefore, this hydrogel microwell array could be a powerful array to regulate the uniform-sized neurosphere-mediated motoneuron differentiation.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectPLURIPOTENT STEM-CELLS-
dc.subjectEMBRYOID BODY FORMATION-
dc.subjectMOTOR-NEURONS-
dc.subjectDIRECTED DIFFERENTIATION-
dc.subjectDISEASE-
dc.subjectCULTURE-
dc.subjectMODELS-
dc.subjectBODIES-
dc.subjectSYSTEM-
dc.titleUniform-sized neurosphere-mediated motoneuron differentiation in microwell arrays-
dc.typeArticle-
dc.contributor.affiliatedAuthorSun, Woong-
dc.identifier.doi10.1002/elps.201700118-
dc.identifier.scopusid2-s2.0-85028816364-
dc.identifier.wosid000417755800012-
dc.identifier.bibliographicCitationELECTROPHORESIS, v.38, no.24, pp.3161 - 3167-
dc.relation.isPartOfELECTROPHORESIS-
dc.citation.titleELECTROPHORESIS-
dc.citation.volume38-
dc.citation.number24-
dc.citation.startPage3161-
dc.citation.endPage3167-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.subject.keywordPlusPLURIPOTENT STEM-CELLS-
dc.subject.keywordPlusEMBRYOID BODY FORMATION-
dc.subject.keywordPlusMOTOR-NEURONS-
dc.subject.keywordPlusDIRECTED DIFFERENTIATION-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusCULTURE-
dc.subject.keywordPlusMODELS-
dc.subject.keywordPlusBODIES-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordAuthorHydrogel microwell array-
dc.subject.keywordAuthorMotoneuron differentiation-
dc.subject.keywordAuthorUniform-sized neurosphere-
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