Greenberger J S, Wright E, Henault S, Anklesaria P, Leif J, Sakakeeny M A, FitzGerald T J, Pierce J H, Kase K
Department of Radiation Oncology, University of Massachusetts Medical Center, Worcester 01655.
Exp Hematol. 1990 Jun;18(5):408-15.
The hematopoietic and stromal cell-specific properties of the cells involved in gamma irradiation leukemogenesis in vitro were defined. Cocultivation of clonal factor-dependent (FD), interleukin 3 (IL-3)-dependent cell lines 32D cl 3 or B6SUtA, or dual IL-3-/granulocyte-macrophage colony-stimulating factor (GM-CSF)-dependent cell lines FDC-P1 or bg/bg d64 was carried out with clonal stromal cell lines D2XRII, GB1/6, +/+ 2.4, or Sld3. FD cell lines were added to control or 5000-cGy-irradiated plateau phase monolayer cultures of each stromal cell line, and parameters of stem cell engraftment and malignant transformation in vitro were quantitated. Cobblestone island formation by FD cells, cumulative production of nonadherent hematopoietic cells, and evolution of tumorigenic factor-independent (FI) subclonal lines were quantitated over 5-8 weeks. There was no detectable evolution of FI sublines with 32D cl 3, B6SUtA, or bg/bg d64 cells cocultivated with control or irradiated Sld3 stromal cells. IL-3-dependent cell lines 32D cl 3 or B6SUtA formed small 10- to 49-cell cobblestone "clusters" at low frequency on control or irradiated D2XRII, showed limited proliferation for less than 1 week, and showed no detectable evolution of FI cell lines. Subclones of 32D cl 3 derived by transfection and expression of recombinant oncogenes v-sis, or c-myc, or the epidermal growth factor receptor remained factor dependent and did not transform to factor independence after cocultivation with irradiated stromal cell lines. In contrast, cell line bg/bg d64, and each of seven subclonal lines of FDC-P1, including subclones selected for growth in GM-CSF, formed abundant cobblestone island colonies of greater than or equal to 50 cells on irradiated D2XRII stromal cells, produced non-adherent cells over 5-8 weeks, and showed evolution of tumorigenic FI subclonal lines. The data provide evidence for stable biological differences in both the hematopoietic and stromal cell components of the in vitro model of gamma irradiation leukemogenesis.
确定了参与体外γ射线照射诱导白血病发生的细胞的造血和基质细胞特异性特性。将克隆的因子依赖性(FD)、白细胞介素3(IL-3)依赖性细胞系32D cl 3或B6SUtA,或双IL-3/粒细胞-巨噬细胞集落刺激因子(GM-CSF)依赖性细胞系FDC-P1或bg/bg d64与克隆的基质细胞系D2XRII、GB1/6、+/+ 2.4或Sld3进行共培养。将FD细胞系添加到每个基质细胞系的对照或5000 cGy照射的平台期单层培养物中,并对体外干细胞植入和恶性转化的参数进行定量。在5至8周内对FD细胞形成的鹅卵石岛、非贴壁造血细胞的累积产生以及致瘤因子非依赖性(FI)亚克隆系的演变进行定量。与对照或照射的Sld3基质细胞共培养的32D cl 3、B6SUtA或bg/bg d64细胞未检测到FI亚系的演变。IL-3依赖性细胞系32D cl 3或B6SUtA在对照或照射的D2XRII上以低频率形成小的10至49细胞的鹅卵石“簇”,增殖受限不到1周,且未检测到FI细胞系的演变。通过转染和表达重组癌基因v-sis、c-myc或表皮生长因子受体衍生的32D cl 3亚克隆在与照射的基质细胞系共培养后仍依赖因子,未转化为因子非依赖性。相反,细胞系bg/bg d64以及FDC-P1的七个亚克隆系中的每一个,包括选择在GM-CSF中生长的亚克隆,在照射的D2XRII基质细胞上形成大量大于或等于50细胞的鹅卵石岛集落,在5至8周内产生非贴壁细胞,并显示出致瘤FI亚克隆系的演变。这些数据为γ射线照射诱导白血病发生的体外模型的造血和基质细胞成分中的稳定生物学差异提供了证据。