자살유전자를 발현하는 레트로바이러스의 이입후 중간엽 줄기세포의 특성에 관한 연구

DC Field Value Language
dc.contributor.advisor서해영, 김성수-
dc.contributor.author박진성-
dc.date.accessioned2019-10-21T07:22:00Z-
dc.date.available2019-10-21T07:22:00Z-
dc.date.issued2013-08-
dc.identifier.other15072-
dc.identifier.urihttps://dspace.ajou.ac.kr/handle/2018.oak/18288-
dc.description학위논문(박사)----아주대학교 일반대학원 :의생명학과,2013. 8-
dc.language.isoeng-
dc.publisherThe Graduate School, Ajou University-
dc.rights아주대학교 논문은 저작권에 의해 보호받습니다.-
dc.title자살유전자를 발현하는 레트로바이러스의 이입후 중간엽 줄기세포의 특성에 관한 연구-
dc.title.alternativeCharacterization of Genetically Modified Mesenchymal Stem Cells with a Retroviral Vector Expressing a Suicide Gene-
dc.typeThesis-
dc.contributor.affiliation아주대학교 일반대학원-
dc.contributor.alternativeNameJin Sung Park-
dc.contributor.department일반대학원 의생명과학과-
dc.date.awarded2013. 8-
dc.description.degreeMaster-
dc.identifier.localId571175-
dc.identifier.urlhttp://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000015072-
dc.subject.keywordmesenchymal stem cell-
dc.subject.keywordretrovirus-
dc.subject.keywordsuicide gene-
dc.subject.keywordgene therapy-
dc.subject.keywordex-vivo therapy-
dc.subject.keywordsafety-
dc.description.alternativeAbstractHuman mesenchymal stem cells have emerged as attractive cellular vehicles to deliver therapeutic genes for ex-vivo therapy of diverse diseases because they have the capability to migrate into tumor or lesion sites. Previously, we showed that mesenchymal stem cells could be utilized as a cellular vehicle to deliver a bacterial cytosine deaminase suicide gene to brain tumors. Here, we assessed whether transduction with a retroviral vector encoding cytosine deaminase gene might alter the stem cell property of mesenchymal stem cells. Mesenchymal stem cells were transduced at passage 1 and cultivated up to passage 11. We found that proliferative and differentiation potential, chromosomal stability and surface antigenicity of mesenchymal stem cells were not altered by retroviral transduction. The results indicate that retroviral vectors can be safely utilized for deliver suicide genes to mesenchymal stem cells for ex-vivo therapy. We also found that the single retroviral transduction was sufficient for the sustainable expression up to passage 10. The long-lasting expression of transduced gene warrants manufacturing the transduced mesenchymal stem cells tractable and manageable for allogeneic transplantation.-
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Graduate School of Ajou University > Department of Biomedical Sciences > 3. Theses(Master)
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