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In vitro expansion of CD34(+)CD38(-) cells under stimulation with hematopoietic growth factors on AGM-S3 cells in juvenile myelomonocytic leukemia.
Sakashita, K; Kato, I; Daifu, T; Saida, S; Hiramatsu, H; Nishinaka, Y; Ebihara, Y; Ma, F; Matsuda, K; Saito, S; Hirabayashi, K; Kurata, T; Uyen, L T N; Nakazawa, Y; Tsuji, K; Heike, T; Nakahata, T; Koike, K.
Afiliação
  • Sakashita K; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
  • Kato I; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Daifu T; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Saida S; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Hiramatsu H; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Nishinaka Y; Department of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan.
  • Ebihara Y; 1] Department of Pediatric Hematology/Oncology, Research Hospital, Institute of Medical Science, University of Tokyo, Minato-ku, Japan [2] Division of Stem Cell Processing, Center for Stem Cell Biology and Regenerative Medicine, Institute of Medical Science, University of Tokyo, Minato-ku, Japan.
  • Ma F; 1] Division of Stem Cell Processing, Center for Stem Cell Biology and Regenerative Medicine, Institute of Medical Science, University of Tokyo, Minato-ku, Japan [2] Institute of Blood Transfusion, Chinese Academy of Medical Sciences and Peking Union Medical College, Chengdu, China.
  • Matsuda K; Department of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan.
  • Saito S; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
  • Hirabayashi K; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
  • Kurata T; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
  • Uyen LT; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
  • Nakazawa Y; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
  • Tsuji K; 1] Department of Pediatric Hematology/Oncology, Research Hospital, Institute of Medical Science, University of Tokyo, Minato-ku, Japan [2] Division of Stem Cell Processing, Center for Stem Cell Biology and Regenerative Medicine, Institute of Medical Science, University of Tokyo, Minato-ku, Japan [3]
  • Heike T; Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Nakahata T; Department of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan.
  • Koike K; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
Leukemia ; 29(3): 606-14, 2015 Mar.
Article em En | MEDLINE | ID: mdl-25102944
ABSTRACT
Using serum-containing culture, we examined whether AGM-S3 stromal cells, alone or in combination with hematopoietic growth factor(s), stimulated the proliferation of CD34(+) cells from patients with juvenile myelomonocytic leukemia (JMML). AGM-S3 cells in concert with stem cell factor plus thrombopoietin increased the numbers of peripheral blood CD34(+) cells to approximately 20-fold of the input value after 2 weeks in nine JMML patients with either PTPN11 mutations or RAS mutations, who received allogeneic hematopoietic transplantation. Granulocyte-macrophage colony-stimulating factor (GM-CSF) also augmented the proliferation of JMML CD34(+) cells on AGM-S3 cells. The expansion potential of CD34(+) cells was markedly low in four patients who achieved spontaneous hematological improvement. A large proportion of day-14-cultured CD34(+) cells were negative for CD38 and cryopreservable. Cultured JMML CD34(+)CD38(-) cells expressed CD117, CD116, c-mpl, CD123, CD90, but not CXCR4, and formed GM and erythroid colonies. Day-7-cultured CD34(+) cells from two of three JMML patients injected intrafemorally into immunodeficient mice stimulated with human GM-CSF after transplantation displayed significant hematopoietic reconstitution. The abilities of OP9 cells and MS-5 cells were one-third and one-tenth, respectively, of the value obtained with AGM-S3 cells. Our culture system may provide a useful tool for elucidating leukemogenesis and for therapeutic approaches in JMML.
Assuntos
Células-Tronco Embrionárias/efeitos dos fármacos; Regulação Leucêmica da Expressão Gênica; Fator Estimulador de Colônias de Granulócitos e Macrófagos/farmacologia; Células-Tronco Hematopoéticas/efeitos dos fármacos; Leucemia Mielomonocítica Juvenil/genética; Células Estromais/efeitos dos fármacos; ADP-Ribosil Ciclase 1/genética; ADP-Ribosil Ciclase 1/metabolismo; Adolescente; Animais; Antígenos CD34/genética; Antígenos CD34/metabolismo; Proliferação de Células/efeitos dos fármacos; Células Clonais; Técnicas de Cocultura; Células-Tronco Embrionárias/metabolismo; Células-Tronco Embrionárias/patologia; GTP Fosfo-Hidrolases/genética; GTP Fosfo-Hidrolases/metabolismo; Células-Tronco Hematopoéticas/metabolismo; Células-Tronco Hematopoéticas/patologia; Humanos; Leucemia Mielomonocítica Juvenil/metabolismo; Leucemia Mielomonocítica Juvenil/patologia; Proteínas de Membrana/genética; Proteínas de Membrana/metabolismo; Camundongos; Camundongos Endogâmicos NOD; Camundongos SCID; Mutação; Células-Tronco Neoplásicas/metabolismo; Células-Tronco Neoplásicas/patologia; Células-Tronco Neoplásicas/transplante; Proteína Tirosina Fosfatase não Receptora Tipo 11/genética; Proteína Tirosina Fosfatase não Receptora Tipo 11/metabolismo; Proteínas Proto-Oncogênicas/genética; Proteínas Proto-Oncogênicas/metabolismo; Proteínas Proto-Oncogênicas p21(ras); Transdução de Sinais; Células Estromais/metabolismo; Células Estromais/patologia; Proteínas ras/genética; Proteínas ras/metabolismo

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Regulação Leucêmica da Expressão Gênica / Fator Estimulador de Colônias de Granulócitos e Macrófagos / Células Estromais / Células-Tronco Embrionárias / Leucemia Mielomonocítica Juvenil Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Regulação Leucêmica da Expressão Gênica / Fator Estimulador de Colônias de Granulócitos e Macrófagos / Células Estromais / Células-Tronco Embrionárias / Leucemia Mielomonocítica Juvenil Idioma: En Ano de publicação: 2015 Tipo de documento: Article