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Chronic Myelogenous Leukemia Cells Contribute to the Stromal Myofibroblasts in Leukemic NOD/SCID MouseIn Vivo
Author(s) -
Ryosuke Shirasaki,
Haruko Tashiro,
Yoko Oka,
Takuji Matsuo,
Tadashi Yamamoto,
Toshihiko Sugao,
Nobu Akiyama,
Kazuo Kawasugi,
Naoki Shirafuji
Publication year - 2012
Publication title -
journal of oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.228
H-Index - 54
eISSN - 1687-8469
pISSN - 1687-8450
DOI - 10.1155/2012/901783
Subject(s) - medicine , nod , chronic myelogenous leukemia , in vivo , leukemia , stromal cell , cancer research , pathology , immunology , genetics , biology , diabetes mellitus , endocrinology
We recently reported that chronic myelogenous leukemia (CML) cells converted into myofibroblasts to create a microenvironment for proliferation of CML cells in vitro . To analyze a biological contribution of CML-derived myofibroblasts in vivo , we observed the characters of leukemic nonobese diabetes/severe combined immunodeficiency (NOD/SCID) mouse. Bone marrow nonadherent mononuclear cells as well as human CD45-positive cells obtained from CML patients were injected to the irradiated NOD/SCID mice. When the chimeric BCR - ABL transcript was demonstrated in blood, human CML cells were detected in NOD/SCID murine bone marrow. And CML-derived myofibroblasts composed with the bone marrow-stroma, which produced significant amounts of human vascular endothelial growth factor A. When the parental CML cells were cultured with myofibroblasts separated from CML cell-engrafted NOD/SCID murine bone marrow, CML cells proliferated significantly. These observations indicate that CML cells make an adequate microenvironment for their own proliferation in vivo .

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