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Anti-death strategies against oxidative stress in grafted mesenchymal stem cells

DC Field Value Language
dc.contributor.author이세연-
dc.contributor.author최은미-
dc.contributor.author최은현-
dc.contributor.author함온주-
dc.contributor.author황기철-
dc.date.accessioned2014-12-18T09:31:16Z-
dc.date.available2014-12-18T09:31:16Z-
dc.date.issued2013-
dc.identifier.issn0213-3911-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/88322-
dc.description.abstractMesenchymal stem cells (MSCs) possess the potential for use in cell-based therapy for repair of myocardial injury. The therapeutic potential of MSCs is based on the capacity of MSCs to differentiate into cardiac tissue and release paracrine factors. However, a major problem in the clinical application of MSC-based therapy is the poor viability of transplanted MSCs at the site of graft due to harsh microenvironment conditions, such as ischemia and/or anoikis. Ischemia after myocardial infarction (MI) and interaction of MSCs with their niche is associated with increased production of reactive oxygen species (ROS). ROS hinder cell adhesion and induce detachment of cells, which induces anoikis signals in implanted MSCs. Therefore, strategies to regulate oxidative stress following the implantation of MSCs are therapeutically attractive. In this review, we first describe ROS as a major obstacle in MSC-based therapy and focus on manipulation of implanted MSCs to reduce ROS-mediated anoikis.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfHISTOLOGY AND HISTOPATHOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnoikis/physiology*-
dc.subject.MESHHumans-
dc.subject.MESHMesenchymal Stem Cell Transplantation*-
dc.subject.MESHMesenchymal Stromal Cells/physiology-
dc.subject.MESHOxidative Stress/physiology*-
dc.subject.MESHReactive Oxygen Species/metabolism-
dc.titleAnti-death strategies against oxidative stress in grafted mesenchymal stem cells-
dc.typeArticle-
dc.contributor.collegeResearcher Institutes (부설 연구소)-
dc.contributor.departmentYonsei Integrative Research Institute for Cerebral & Cardiovascular Disease (뇌심혈관질환융합연구사업단)-
dc.contributor.googleauthorWoochul Chang-
dc.contributor.googleauthorByeong-Wook Song-
dc.contributor.googleauthorJae-Youn Moon-
dc.contributor.googleauthorMin-Ji Cha-
dc.contributor.googleauthorOnju Ham-
dc.contributor.googleauthorSe-Yeon Lee-
dc.contributor.googleauthorEunmi Choi-
dc.contributor.googleauthorEunhyun Choi-
dc.contributor.googleauthorKi-Chul Hwang-
dc.identifier.doi10.14670/HH-28.1529-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02880-
dc.contributor.localIdA04162-
dc.contributor.localIdA04336-
dc.contributor.localIdA04456-
dc.contributor.localIdA04151-
dc.relation.journalcodeJ00993-
dc.identifier.eissn1699-5848-
dc.identifier.pmid23760682-
dc.identifier.urlhttp://www.hh.um.es/Abstracts/Vol_28/28_12/28_12_1529.htm-
dc.subject.keywordMesenchymal stem cells-
dc.subject.keywordReactive oxygen species-
dc.subject.keywordAnoikis-
dc.subject.keywordMyocardial infarction-
dc.contributor.alternativeNameLee, Se Yeon-
dc.contributor.alternativeNameChoi, Eun Mi-
dc.contributor.alternativeNameChoi, Eun Hyun-
dc.contributor.alternativeNameHam, On Ju-
dc.contributor.alternativeNameHwang, Ki Chul-
dc.contributor.affiliatedAuthorLee, Se Yeon-
dc.contributor.affiliatedAuthorChoi, Eun Hyun-
dc.contributor.affiliatedAuthorHam, On Ju-
dc.contributor.affiliatedAuthorHwang, Ki Chul-
dc.contributor.affiliatedAuthorChoi, Eun Mi-
dc.rights.accessRightsnot free-
dc.citation.volume28-
dc.citation.number12-
dc.citation.startPage1529-
dc.citation.endPage1536-
dc.identifier.bibliographicCitationHISTOLOGY AND HISTOPATHOLOGY, Vol.28(12) : 1529-1536, 2013-
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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