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c-kit Ligand가 Transforming Growth-Factor-β1(TGF-β1)에 의한 CD34^(+) 급성 골수성백혈병세포의 Apoptosis에 미치는 영향

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dc.contributor.author민유홍-
dc.date.accessioned2021-12-27T17:19:08Z-
dc.date.available2021-12-27T17:19:08Z-
dc.date.issued1995-12-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/186550-
dc.description.abstractBackground: Transforming growth factor-β1(TGF-β1) induces a inhibition of blast clonogenic cells in suspension and methylcellulose cultures. But the mechanisms of inhibition of leukemic clonogenic cells are not known exactly. We evaluated quantitatively the TGF-β1-induced apoptosis of CD34-positive(CD34+) acute myeloid leukemic(AML) cells because TGF-β1 is one of the representative cytokines that induce cell death by apoptotic mechanism. And we investigated the role of c-kit ligand(stem cell factor; SCF) with or without granulocyte-macrophage colony-stimulating factor(GM-CSF) and/or interleukin-3(IL-3) in the inhibition of TGF-β1-induced apoptosis of CD34+ AML cells. Materials and Methods: CD34+ AML cells were isolated from the bone marrow of 14 patients with AML using immunomagnectic microbead method. The various combination of cytokines including TGF-β1, SCF, GM-CSF, and IL-β1, was used to study the quantitation of colony formation in methylcellulose and of apoptosis of CD34+ AML cells in vitro. Analysis of apoptosis was done by ELISA method using Cell Death Detection kit. Results: SCF alone resulted in no significant colony formation, while the combination of SCF plus GM-CSF and/or IL-β1 stimulated significant colony formation. The addition of TGF-β1 alone to culture of CD34+ AML cells resulted in total inhibition of colony formation. The combination of SCF plus TGF-β1 also did not result in colony formation. But no significant inhibition of colony formation was obtained for the combination of SCF plus GM-CSF by TGF-β1. Our study demonstrated that TGF-β1 induces apoptosis in CD34+ AML cells. This TGF-β1-induced apoptosis was not inhibited by SCF alone. The combination of SCF and IL-3 showed a marginal effect. But the TGF-β1-induced apoptosis of CD34+ AML cells was significantly inhibited by SCF plus GM-CSF (P<0.05) or SCF and GM-CSF plus IL-3(p<0.05). This pattern of inhibition of TGF-β1-induced apoptosis by costimulating effect of SCF was also observed for the CD34+ normal bone marrow cells, but not for CD34- AML cells. Conclusion: This study showed that costimulatory effect of c-kit ligand, with GM-CSF or GM-CSF plus IL-3, can inhibit the TGF-β1-induced apoptosis preferentially in CD34+ AML cells rather than the CD34- AML cells. And we suggest that the TGF-β1-induced growth inhibition of clonogenic leukemic cells may be associated with the TGF-β1-induced apoptosis of clonogenic leukemic cells.-
dc.description.statementOfResponsibilityprohibition-
dc.languageKorean-
dc.publisher한국BRM학회-
dc.relation.isPartOfKorean Journal of Biological Response Modifiers(한국 BRM학회지)-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titlec-kit Ligand가 Transforming Growth-Factor-β1(TGF-β1)에 의한 CD34^(+) 급성 골수성백혈병세포의 Apoptosis에 미치는 영향-
dc.title.alternativeEffect of c-kit Ligand on the Transforming Growth Factor-β1(TGF-β1)-induced Apoptosis of CD34^(+) Acute Myeloid Leukemin Cells-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthor민유홍-
dc.contributor.googleauthor김성철-
dc.contributor.googleauthor이승태-
dc.contributor.googleauthor한지숙-
dc.contributor.googleauthor고윤웅-
dc.contributor.localIdA01407-
dc.relation.journalcodeJ03698-
dc.subject.keywordc-kit ligand-
dc.subject.keywordTGF-β1-
dc.subject.keywordCD34^(+)-
dc.subject.keywordAML-
dc.subject.keywordApoptosis-
dc.contributor.alternativeNameMin, Yoo Hong-
dc.contributor.affiliatedAuthor민유홍-
dc.citation.volume5-
dc.citation.number2-
dc.citation.startPage195-
dc.citation.endPage207-
dc.identifier.bibliographicCitationKorean Journal of Biological Response Modifiers (한국 BRM학회지), Vol.5(2) : 195-207, 1995-12-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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