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dc.contributor.author정성민*
dc.contributor.author유경하*
dc.contributor.author최병옥*
dc.contributor.author우소연*
dc.contributor.author김한수*
dc.contributor.author정성철*
dc.contributor.author조인호*
dc.contributor.author최윤희*
dc.contributor.author박영미*
dc.contributor.author조경아*
dc.contributor.author박혜상*
dc.date.accessioned2016-08-28T10:08:02Z-
dc.date.available2016-08-28T10:08:02Z-
dc.date.issued2012*
dc.identifier.issn1465-3249*
dc.identifier.otherOAK-9459*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/223181-
dc.description.abstractBackground aims. Although mesenchymal stromal cells (MSC) from human palatine tonsils (tonsillar MSC, T-MSC) have been isolated, whether T-MSC isolated from multiple donors are feasible for cell banking has not been studied. Methods. T-MSC before and after a standard protocol of cryopreservation and thawing were assessed regarding several basic characteristics, including colony-forming unitfibroblast features, MSC-specific surface antigen profiles, and inhibition of alloreactive T-cell proliferation. In vitro mesodermal differentiation potentials to adipocytes, osteocytes and chondrocytes were detected by staining with either cell-specific dyes or antibody after incubation with each appropriate differentiation medium. Expression of mesoderm-specific genes was also quantified by real-time polymerase chain reaction (PCR) assay. Expression profiles of endoderm-specific genes were identified by reverse transcription PCR assay. The feasibility of T-MSC in future engraftment was tested by short tandem repeat (STR) analysis using genomic DNA isolated randomly from three independent subjects. Results. Both fresh and cryopreservedthawed T-MSC showed a similar high proliferation capacity and expressed primitive cell-surface markers. Hematopoietic cell markers, HLA-DR, co-stimulatory molecules and follicular dendritic cell markers were not detected. In addition to mesodermal differentiation, fresh and cryopreservedthawed cells also underwent endodermal differentiation, as evidenced by the expression of endoderm-specific genes including forkhead box A2 (FoxA2), SIX homeobox 1 (Six1) and chemokine (C-C motif) ligand 21 (CCL21). Both cells significantly decreased phorbol 12- myristate 13-acetate (PMA)-induced T-cell proliferation. T-MSC from three independent donors formed chimerism in STR analysis. Conclusions. Our results demonstrate for the first time that T-MSC are a potentially good source for MSC banking. © 2012 Informa Healthcare.*
dc.languageEnglish*
dc.titleTonsil-derived mesenchymal stromal cells: Evaluation of biologic, immunologic and genetic factors for successful banking*
dc.typeArticle*
dc.relation.issue10*
dc.relation.volume14*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1193*
dc.relation.lastpage1202*
dc.relation.journaltitleCytotherapy*
dc.identifier.doi10.3109/14653249.2012.706708*
dc.identifier.wosidWOS:000311182800006*
dc.identifier.scopusid2-s2.0-84867657065*
dc.author.googleRyu K.-H.*
dc.author.googleCho K.-A.*
dc.author.googlePark H.S.*
dc.author.googleKim J.-Y.*
dc.author.googleWoo S.-Y.*
dc.author.googleJo I.*
dc.author.googleChoi Y.H.*
dc.author.googlePark Y.M.*
dc.author.googleJung S.-C.*
dc.author.googleChung S.M.*
dc.author.googleChoi B.-O.*
dc.author.googleKim H.S.*
dc.contributor.scopusid정성민(37042902400)*
dc.contributor.scopusid유경하(14038236200)*
dc.contributor.scopusid최병옥(7402755390)*
dc.contributor.scopusid우소연(7402853365)*
dc.contributor.scopusid김한수(56509934900)*
dc.contributor.scopusid정성철(57008539100)*
dc.contributor.scopusid조인호(26643129000;56663841900)*
dc.contributor.scopusid최윤희(7404776849)*
dc.contributor.scopusid박영미(7405372677)*
dc.contributor.scopusid조경아(21734204400)*
dc.date.modifydate20240422114059*
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의과대학 > 의학과 > Journal papers
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