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Cited 5 time in webofscience Cited 5 time in scopus
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dc.contributor.authorJung, Taek-Hee-
dc.contributor.authorChung, Eun-Bin-
dc.contributor.authorKIM, HYUNG WOO-
dc.contributor.authorChoi, Seong Woo-
dc.contributor.authorPark, Soon-Jung-
dc.contributor.authorMukhtar, Anthony Safaa-
dc.contributor.authorChung, Hyung-Min-
dc.contributor.authorKim, Eunmi-
dc.contributor.authorHuh, Kang Moo-
dc.contributor.authorKIM, DONG SUNG-
dc.contributor.authorKang, Sun-Woong-
dc.contributor.authorMoon, Sung-Hwan-
dc.date.accessioned2020-09-07T00:50:37Z-
dc.date.available2020-09-07T00:50:37Z-
dc.date.created2020-06-07-
dc.date.issued2020-05-
dc.identifier.issn1932-6203-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/104106-
dc.description.abstractVarious nanopatterning techniques have been developed to improve cell proliferation and differentiation efficiency. As we previously reported, nanopillars and pores are able to sustain human pluripotent stem cells and differentiate pancreatic cells. From this, the nanoscale patterns would be effective environment for the co-culturing of epithelial and mesenchymal cell types. Interestingly, the nanopatterning selectively reduced the proliferative rate of mesenchymal cells while increasing the expression of adhesion protein in epithelial type cells. Additionally, co-cultured cells on the nanopatterning were not negatively affected in terms of cell function metabolic ability or cell survival. This is in contrast to conventional co-culturing methods such as ultraviolet or chemical treatments. The nanopatterning appears to be an effective environment for mesenchymal co-cultures with typically low proliferative rates cells such as astrocytes, neurons, melanocytes, and fibroblasts without using potentially damaging treatments.-
dc.languageEnglish-
dc.publisherPublic Library of Science-
dc.relation.isPartOfPLoS ONE-
dc.titleApplication of Co-culture Technology of Epithelial Type Cells and Mesenchymal Type Cells Using Nanopatterned Structures-
dc.typeArticle-
dc.identifier.doi10.1371/journal.pone.0232899-
dc.type.rimsART-
dc.identifier.bibliographicCitationPLoS ONE, v.15, no.5, pp.e0232899-
dc.identifier.wosid000537470300030-
dc.citation.number5-
dc.citation.startPagee0232899-
dc.citation.titlePLoS ONE-
dc.citation.volume15-
dc.contributor.affiliatedAuthorKIM, HYUNG WOO-
dc.contributor.affiliatedAuthorKIM, DONG SUNG-
dc.identifier.scopusid2-s2.0-85084508192-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.type.docTypeArticle-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusMITOMYCIN-C-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusPERSPECTIVE-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusASSAY-
dc.subject.keywordPlusFATE-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-

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김동성KIM, DONG SUNG
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