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Senescence of fetal endothelial progenitor cell in pregnancy with idiopathic fetal growth

DC Field Value Language
dc.contributor.author권자영-
dc.contributor.author김영한-
dc.contributor.author박용원-
dc.date.accessioned2014-12-19T17:11:51Z-
dc.date.available2014-12-19T17:11:51Z-
dc.date.issued2012-
dc.identifier.issn1476-7058-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/90957-
dc.description.abstractOBJECTIVE: The aim of our study was to investigate the change of count and the status of cellular senescence in fetal endothelial progenitor cells (EPCs) obtained from the umbilical cord blood of women with fetal growth restriction (FGR). METHODS: Fetal EPCs were obtained from thirty five normal and thirty pregnant women with FGR. Each EPC was characterized and counted. EPC differentiation time and outgrowth endothelial cell (OEC) colony formation assay, senescence-associated β-galactosidase (SA-β-gal) activity assay, and telomerase activity assay were performed. RESULTS: Fetal EPC counts were significantly decreased in the FGR group compared with normal controls. In the FGR group, the EPC differentiation time was prolonged, OEC colonies were much less formed, the staining intensity of SA-β-gal was relatively increased and the telomerase activity of EPCs was significantly decreased, compared with normal pregnancy (p < 0.001 for all). CONCLUSIONS: The fetal EPCs in FGR pregnancies were decreased, functionally impaired and senescently altered.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfJOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHCase-Control Studies-
dc.subject.MESHCell Differentiation/physiology-
dc.subject.MESHCell Proliferation-
dc.subject.MESHCell Separation-
dc.subject.MESHCells, Cultured-
dc.subject.MESHCellular Senescence/physiology*-
dc.subject.MESHEndothelial Cells/cytology-
dc.subject.MESHEndothelial Cells/pathology*-
dc.subject.MESHEndothelial Cells/physiology*-
dc.subject.MESHFemale-
dc.subject.MESHFetal Growth Retardation/diagnostic imaging-
dc.subject.MESHFetal Growth Retardation/pathology*-
dc.subject.MESHFetal Growth Retardation/physiopathology-
dc.subject.MESHFetal Stem Cells/cytology-
dc.subject.MESHFetal Stem Cells/pathology-
dc.subject.MESHFetal Stem Cells/physiology*-
dc.subject.MESHHumans-
dc.subject.MESHInfant, Newborn-
dc.subject.MESHPregnancy-
dc.subject.MESHUltrasonography-
dc.titleSenescence of fetal endothelial progenitor cell in pregnancy with idiopathic fetal growth-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Obstetrics & Gynecology (산부인과학)-
dc.contributor.googleauthorHan Sung Hwang-
dc.contributor.googleauthorYoung Guen Kwon-
dc.contributor.googleauthorJa Young Kwon-
dc.contributor.googleauthorYong Won Park-
dc.contributor.googleauthorYong Sun Maeng-
dc.contributor.googleauthorYoung Han Kim-
dc.identifier.doi22339619-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00246-
dc.contributor.localIdA00730-
dc.contributor.localIdA01581-
dc.relation.journalcodeJ01577-
dc.identifier.eissn1476-4954-
dc.identifier.pmid22339619-
dc.identifier.urlhttp://informahealthcare.com/doi/abs/10.3109/14767058.2012.663826-
dc.subject.keywordEndothelial progenitor cell-
dc.subject.keywordfetal growth restriction-
dc.subject.keywordsenescence-
dc.contributor.alternativeNameKwon, Ja Young-
dc.contributor.alternativeNameKim, Young Han-
dc.contributor.alternativeNamePark, Yong Won-
dc.contributor.affiliatedAuthorKwon, Ja Young-
dc.contributor.affiliatedAuthorKim, Young Han-
dc.contributor.affiliatedAuthorPark, Yong Won-
dc.citation.volume25-
dc.citation.number9-
dc.citation.startPage1769-
dc.citation.endPage1773-
dc.identifier.bibliographicCitationJOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, Vol.25(9) : 1769-1773, 2012-
dc.identifier.rimsid33240-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers

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