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Are Adipose-Derived Stem Cells From Liver Falciform Ligaments Another Possible Source of Mesenchymal Stem Cells?

DC Field Value Language
dc.contributor.author김경식-
dc.contributor.author정재욱-
dc.date.accessioned2017-11-02T08:22:52Z-
dc.date.available2017-11-02T08:22:52Z-
dc.date.issued2017-
dc.identifier.issn0963-6897-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/154401-
dc.description.abstractFalciform ligaments in the liver are surrounded by adipose tissue. We investigated the capability of adipose-derived stem cells from human liver falciform ligaments (hLF-ADSCs) to differentiate into hepatic-type cells and confirmed the functional capacity of the cells. Mesenchymal stem cells (MSCs) were isolated from the liver falciform ligament and abdominal subcutaneous adipose tissue in patients undergoing partial hepatectomy for liver disease. Cells were cultivated in MSC culture medium. Properties of MSCs were confirmed by flow cytometry, RT-PCR analysis, immunocytochemistry assays, and multilineage differentiation. Hepatic induction was performed using a three-step differentiation protocol with various growth factors. Morphology, capacity for expansion, and characteristics were similar between hLF-ADSCs and adipose-derived stem cells from human abdominal subcutaneous adipose tissue (hAS-ADSCs). However, hematopoietic- and mesenchymal-epithelial transition (MET)-related surface markers (CD133, CD34, CD45, and E-cadherin) had a higher expression in hLF-ADSCs. The hepatic induction marker genes had a higher expression in hLF-ADSCs on days 7 and 10 after the hepatic induction. Albumin secretion was similar between hLF-ADSCs and hAS-ADSCs at 20 days after the hepatic induction. The hLF-ADSCs had a different pattern of surface marker expression relative to hAS-ADSCs. However, proliferation, multilineage capacity, and hepatic induction were similar between the cell types. Accordingly, it may be a useful source of MSCs for patients with liver disease.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherCognizant Communication-
dc.relation.isPartOfCELL TRANSPLANTATION-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAC133 Antigen/metabolism-
dc.subject.MESHAdipose Tissue/cytology*-
dc.subject.MESHAntigens, CD34/metabolism-
dc.subject.MESHCadherins/metabolism-
dc.subject.MESHCell Differentiation/genetics-
dc.subject.MESHCell Differentiation/physiology*-
dc.subject.MESHCell- and Tissue-Based Therapy/methods-
dc.subject.MESHCells, Cultured-
dc.subject.MESHFlow Cytometry-
dc.subject.MESHHumans-
dc.subject.MESHImmunohistochemistry-
dc.subject.MESHLeukocyte Common Antigens/metabolism-
dc.subject.MESHLiver/cytology-
dc.subject.MESHLiver/metabolism-
dc.subject.MESHMesenchymal Stromal Cells/cytology*-
dc.subject.MESHMesenchymal Stromal Cells/physiology-
dc.subject.MESHReverse Transcriptase Polymerase Chain Reaction-
dc.titleAre Adipose-Derived Stem Cells From Liver Falciform Ligaments Another Possible Source of Mesenchymal Stem Cells?-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Surgery-
dc.contributor.googleauthorSang Woo Lee-
dc.contributor.googleauthorJae Uk Chong-
dc.contributor.googleauthorSeon Ok Min-
dc.contributor.googleauthorSeon Young Bak-
dc.contributor.googleauthorKyung Sik Kim-
dc.identifier.doi10.3727/096368916X693833-
dc.contributor.localIdA03710-
dc.contributor.localIdA00299-
dc.relation.journalcodeJ00492-
dc.identifier.eissn1555-3892-
dc.identifier.pmid27938473-
dc.identifier.urlhttp://www.ingentaconnect.com/contentone/cog/ct/2017/00000026/00000005/art00011?crawler=true-
dc.subject.keywordAdipose tissue-
dc.subject.keywordMesenchymal stem cells (MSCs)-
dc.subject.keywordLiver-
dc.subject.keywordOrgan specificity-
dc.subject.keywordCell therapy-
dc.contributor.alternativeNameKim, Kyung Sik-
dc.contributor.alternativeNameChong, Jae Uk-
dc.contributor.affiliatedAuthorChong, Jae Uk-
dc.contributor.affiliatedAuthorKim, Kyung Sik-
dc.citation.titleCell Transplantation-
dc.citation.volume26-
dc.citation.number5-
dc.citation.startPage855-
dc.citation.endPage866-
dc.identifier.bibliographicCitationCELL TRANSPLANTATION, Vol.26(5) : 855-866, 2017-
dc.date.modified2017-11-01-
dc.identifier.rimsid42976-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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