Cited 6 times in

Ectopic Hard Tissue Formation by Odonto/Osteogenically In Vitro Differentiated Human Deciduous Teeth Pulp Stem Cells

DC Field Value Language
dc.contributor.author김성오-
dc.contributor.author김승혜-
dc.contributor.author송제선-
dc.contributor.author신동민-
dc.contributor.author이제호-
dc.contributor.author전미정-
dc.date.accessioned2016-02-04T11:32:20Z-
dc.date.available2016-02-04T11:32:20Z-
dc.date.issued2015-
dc.identifier.issn0171-967X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/140651-
dc.description.abstractThere have been many attempts to use the pulp tissue from human deciduous teeth for dentin or bone regeneration. The objective of this study was to determine the effects of odonto/osteogenic in vitro differentiation of deciduous teeth pulp stem cells (DTSCs) on their in vivo hard tissue-forming potential. DTSCs were isolated from extracted deciduous teeth using the outgrowth method. These cells were exposed to odonto/osteogenic stimuli for 4 and 8 days (Day 4 and Day 8 groups, respectively), while cells in the control group were cultured in normal medium. The in vitro differentiated DTSCs and the control DTSCs were transplanted subcutaneously into immunocompromised mice with macroporous biphasic calcium phosphate and sacrificed at 8 weeks post-implantation. The effect of odonto/osteogenic in vitro differentiation was evaluated using alkaline phosphatase (ALP) staining and quantitative reverse transcription polymerase chain reaction (RT-PCR). The in vivo effect was evaluated by qualitative RT-PCR, assessment of ALP activity, histologic analysis, and immunohistochemical staining. The amount of hard tissue was greater in Day 4 group than Day 8 group (p = 0.014). However, Day 8 group generated lamellar bone-like structure, which was immunonegative to anti-human dentin sialoprotein with significantly low expression level of DSPP compared with the control group (p = 0.008). This study demonstrates that odonto/osteogenic in vitro differentiation of DTSCs enhances the formation of bone-like tissue, instead of dentin-like tissue, when transplanted subcutaneously using MBCP as a carrier. The odonto/osteogenic in vitro differentiation of DTSCs may be an effective modification that enhances in vivo bone formation by DTSCs.-
dc.description.statementOfResponsibilityopen-
dc.format.extent80~89-
dc.relation.isPartOfCALCIFIED TISSUE INTERNATIONAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHBone Regeneration/physiology*-
dc.subject.MESHCell Differentiation/physiology*-
dc.subject.MESHCell Proliferation/physiology-
dc.subject.MESHCells, Cultured-
dc.subject.MESHDental Pulp/cytology*-
dc.subject.MESHHumans-
dc.subject.MESHMice-
dc.subject.MESHOsteogenesis/physiology*-
dc.subject.MESHStem Cells/cytology*-
dc.subject.MESHTooth, Deciduous/cytology*-
dc.titleEctopic Hard Tissue Formation by Odonto/Osteogenically In Vitro Differentiated Human Deciduous Teeth Pulp Stem Cells-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Oral Biology (구강생물학)-
dc.contributor.googleauthorSeunghye Kim-
dc.contributor.googleauthorJe Seon Song-
dc.contributor.googleauthorMijeong Jeon-
dc.contributor.googleauthorDong Min Shin-
dc.contributor.googleauthorSeong-Oh Kim-
dc.contributor.googleauthorJae Ho Lee-
dc.identifier.doi10.1007/s00223-015-9989-1-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00577-
dc.contributor.localIdA02058-
dc.contributor.localIdA02091-
dc.contributor.localIdA03134-
dc.contributor.localIdA03511-
dc.contributor.localIdA00664-
dc.relation.journalcodeJ00425-
dc.identifier.eissn1432-0827-
dc.identifier.pmid25894066-
dc.identifier.urlhttp://link.springer.com/article/10.1007%2Fs00223-015-9989-1-
dc.subject.keywordDeciduous teeth pulp stem cell-
dc.subject.keywordOdonto/osteogenic in vitro differentiation-
dc.subject.keywordHard tissue-
dc.contributor.alternativeNameKim, Seong Oh-
dc.contributor.alternativeNameKim, Seung Hye-
dc.contributor.alternativeNameSong, Je Seon-
dc.contributor.alternativeNameShin, Dong Min-
dc.contributor.alternativeNameLee, Jae Ho-
dc.contributor.alternativeNameJeon, Mi Jeong-
dc.contributor.affiliatedAuthorKim, Seong Oh-
dc.contributor.affiliatedAuthorSong, Je Seon-
dc.contributor.affiliatedAuthorShin, Dong Min-
dc.contributor.affiliatedAuthorLee, Jae Ho-
dc.contributor.affiliatedAuthorJeon, Mi Jeong-
dc.contributor.affiliatedAuthorKim, Seung Hye-
dc.rights.accessRightsnot free-
dc.citation.volume97-
dc.citation.number1-
dc.citation.startPage80-
dc.citation.endPage89-
dc.identifier.bibliographicCitationCALCIFIED TISSUE INTERNATIONAL, Vol.97(1) : 80-89, 2015-
dc.identifier.rimsid30226-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Research Institute (부설연구소) > 1. Journal Papers
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers
2. College of Dentistry (치과대학) > Dept. of Pediatric Dentistry (소아치과학교실) > 1. Journal Papers

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