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미성숙 매복지치의 치낭, 치수, 치근유두 조직에서 다능성 줄기세포의 분리와 특성화에 대한 연구

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dc.contributor.author송정호-
dc.contributor.author박봉욱-
dc.contributor.author변준호-
dc.contributor.author강은주-
dc.contributor.author노규진-
dc.contributor.author신상훈-
dc.contributor.author김욱규-
dc.contributor.author김종렬-
dc.date.accessioned2022-12-27T04:47:10Z-
dc.date.available2022-12-27T04:47:10Z-
dc.date.issued2010-
dc.identifier.issn2234-7550-
dc.identifier.issn2234-5930-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/25709-
dc.description.abstractIntroduction: The first aim of this study was to isolate the dental tissue-derived stem cells from the dental follicle (DF), dental pulp (DP), and root apical papilla (RAP) of the extracted wisdom teeth. Second was to evaluate their characterization with the expressions of transcription factors and cell surface markers. Finally, their ability of the in vitro multi-lineage differentiations into osteogenic and adipogenic cells were compared, respectively. Materials and Methods: Dental tissues, including dental follicle, dental pulp, and root apical papilla, were separated in the extracted wisdom teeth. These three dental tissues were cultured in Dulbecco’s modified Eagle’s medium (DMEM) with supplements, respectively. After passage 3, the homogeneous shaped dental tissue-derived cells were analyzed the expression of transcription factors (Oct-4, Nanog and Sox-2) and cell surface markers (CD44, CD90 and CD105) with reverse transcription polymerase chain reaction (RT-PCR) and fluorescence-activated cell sorting (FACS) analysis. In order to evaluate in vitro multi-lineage differentiations, the culture media were changed to the osteogenic and adipogenic induction mediums when the dental tissue-derived cells reached to passage 3. The characteristics of these three dental tissue-derived cells were compared with immunohistochemistry. Results: During primary culture, heterogenous and colony formatted dental tissue-derived cells were observed in the culture plates. After passage 2or 3, homogenous spindle-like cells were observed in all culture plates. Transcription factors and mesenchymal stem cell markers were positively observed in all three types of dental tissue-derived cells. However, the quantity of expressed transcription factors was most large in RAP-derived cells. In all three types of dental tissue-derived cells, osteogenic and adipogenic differentiations were observed after treatment of specific induction media. In vitro adipogenic differentiation was similar among these three types of cells. In vitro osteogenic differentiation was most strongly and frequently observed in the RAP-derived cells, whereas rarely osteogenic differentiation was observed in the DP-derived cells. Conclusion: These findings suggest that three types of human dental tissue-derived cells from extracted wisdom teeth were multipotent mesenchymal stem cells, have the properties of multi-lineage differentiations. Especially, stem cells from root apical papilla (SCAP) have much advantage in osteogenic differentiation, whereas dental follicle cells (DFCs) have a characteristic of easy adipogenic differentiation.-
dc.format.extent11-
dc.language한국어-
dc.language.isoKOR-
dc.publisher대한구강악안면외과학회-
dc.title미성숙 매복지치의 치낭, 치수, 치근유두 조직에서 다능성 줄기세포의 분리와 특성화에 대한 연구-
dc.title.alternativeIsolation and characterization of human dental tissue-derived stem cells in the impacted wisdom teeth: comparison of dental follicle, dental pulp, and root apical papilla-derived cells-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.bibliographicCitation대한구강악안면외과학회지, v.36, no.3, pp 186 - 196-
dc.citation.title대한구강악안면외과학회지-
dc.citation.volume36-
dc.citation.number3-
dc.citation.startPage186-
dc.citation.endPage196-
dc.identifier.kciidART001457399-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasskci-
dc.subject.keywordAuthorHuman dental tissue-derived stem cells-
dc.subject.keywordAuthorDental pulp stem cells (DPSCs)-
dc.subject.keywordAuthorDental follicle cells (DFCs)-
dc.subject.keywordAuthorStem cells from root apical papilla (SCAP)-
dc.subject.keywordAuthorMesenchymal stem cells (MSCs)-
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