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Dental pulp of the third molar: a new source of pluripotent-like stem cells

DC Field Value Language
dc.contributor.author정한성-
dc.date.accessioned2014-12-19T17:02:32Z-
dc.date.available2014-12-19T17:02:32Z-
dc.date.issued2012-
dc.identifier.issn0021-9533-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/90667-
dc.description.abstractDental pulp is particularly interesting in regenerative medicine because of the accessibility and differentiation potential of the tissue. Dental pulp has an early developmental origin with multi-lineage differentiation potential as a result of its development during childhood and adolescence. However, no study has previously identified the presence of stem cell populations with embryonic-like phenotypes in human dental pulp from the third molar. In the present work, we describe a new population of dental pulp pluripotent-like stem cells (DPPSCs) that were isolated by culture in medium containing LIF, EGF and PDGF. These cells are SSEA4(+), OCT3/4(+), NANOG(+), SOX2(+), LIN28(+), CD13(+), CD105(+), CD34(-), CD45(-), CD90(+), CD29(+), CD73(+), STRO1(+) and CD146(-), and they show genetic stability in vitro based on genomic analysis with a newly described CGH technique. Interestingly, DPPSCs were able to form both embryoid-body-like structures (EBs) in vitro and teratoma-like structures that contained tissues derived from all three embryonic germ layers when injected in nude mice. We examined the capacity of DPPSCs to differentiate in vitro into tissues that have similar characteristics to mesoderm, endoderm and ectoderm layers in both 2D and 3D cultures. We performed a comparative RT-PCR analysis of GATA4, GATA6, MIXL1, NANOG, OCT3/4, SOX1 and SOX2 to determine the degree of similarity between DPPSCs, EBs and human induced pluripotent stem cells (hIPSCs). Our analysis revealed that DPPSCs, hIPSC and EBs have the same gene expression profile. Because DPPSCs can be derived from healthy human molars from patients of different sexes and ages, they represent an easily accessible source of stem cells, which opens a range of new possibilities for regenerative medicine.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.relation.isPartOfJOURNAL OF CELL SCIENCE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdolescent-
dc.subject.MESHAdult-
dc.subject.MESHAnimals-
dc.subject.MESHCell Differentiation/physiology-
dc.subject.MESHCell Growth Processes/physiology-
dc.subject.MESHDental Pulp/cytology*-
dc.subject.MESHDental Pulp/metabolism-
dc.subject.MESHDental Pulp/physiology-
dc.subject.MESHEmbryoid Bodies/cytology-
dc.subject.MESHFemale-
dc.subject.MESHFlow Cytometry/methods-
dc.subject.MESHHumans-
dc.subject.MESHImmunophenotyping-
dc.subject.MESHInduced Pluripotent Stem Cells/cytology*-
dc.subject.MESHInduced Pluripotent Stem Cells/metabolism-
dc.subject.MESHInduced Pluripotent Stem Cells/physiology-
dc.subject.MESHMale-
dc.subject.MESHMesoderm/cytology-
dc.subject.MESHMice-
dc.subject.MESHMice, Nude-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMolar, Third/cytology*-
dc.subject.MESHMolar, Third/metabolism-
dc.subject.MESHPluripotent Stem Cells/cytology*-
dc.subject.MESHPluripotent Stem Cells/metabolism-
dc.subject.MESHPluripotent Stem Cells/physiology-
dc.subject.MESHTranscriptome-
dc.subject.MESHYoung Adult-
dc.titleDental pulp of the third molar: a new source of pluripotent-like stem cells-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Oral Biology (구강생물학)-
dc.contributor.googleauthorMaher Atari-
dc.contributor.googleauthorCarlos Gil-Recio-
dc.contributor.googleauthorMarc Fabregat-
dc.contributor.googleauthorDani Garcı´a-Ferna´ndez-
dc.contributor.googleauthorMiguel Barajas-
dc.contributor.googleauthorMiguel A. Carrasco-
dc.contributor.googleauthorHan-Sung Jung-
dc.contributor.googleauthorF. Herna´ndez Alfaro-
dc.contributor.googleauthorNuria Casals-
dc.contributor.googleauthorFelipe Prosper-
dc.contributor.googleauthorEduard Ferre´s-Padro-
dc.contributor.googleauthorLuis Giner-
dc.identifier.doi10.1242/jcs.096537-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03758-
dc.relation.journalcodeJ01301-
dc.identifier.eissn1477-9137-
dc.identifier.pmid22467856-
dc.subject.keywordDental pulp-
dc.subject.keywordDPPSC-
dc.subject.keywordPluripotency-
dc.subject.keywordTeratoma formation-
dc.subject.keywordEmbryonic markers-
dc.subject.keywordCGH technique-
dc.contributor.alternativeNameJung, Han Sung-
dc.contributor.affiliatedAuthorJung, Han Sung-
dc.citation.volume125-
dc.citation.numberpt 14-
dc.citation.startPage3343-
dc.citation.endPage3356-
dc.identifier.bibliographicCitationJOURNAL OF CELL SCIENCE, Vol.125(pt 14) : 3343-3356, 2012-
dc.identifier.rimsid33454-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers

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