Naparstek E, Pierce J, Metcalf D, Shadduck R, Ihle J, Leder A, Sakakeeny M A, Wagner K, Falco J, FitzGerald T J
Blood. 1986 May;67(5):1395-403.
We studied the production of hemopoietins by x-irradiated plateau-phase cultures of cloned marrow stromal cell lines derived from C3H/HeJ marrow, termed D2XRII and clone 11. The production of CSF in agar overlay of control or 10,000 rad irradiated stromal cultures was quantitated by induction of colonies in: overlaid fresh marrow, IL-3-dependent cell line 32D cl 3, or GM-CSF/IL-3-dependent cell lines FDCP-1 or bg/bg cl 1. Conditioned media were tested for CSF by bioassay using fresh marrow cells, for M-CSF (CSF-1) by RIA, and for IL-3 and GM-CSF by microwell proliferation assay with 32D cl 3 and FDCP-1 cells, respectively. X-irradiation to doses that decreased CSF-1 to 40% of control levels (greater than 5,000 rad) resulted in a 30-fold increase in growth of FDCP-1 or bg/bg cl 1 cells in liquid co-culture or agar culture overlay with no detectable growth of 32D cl 3. The frequency of subculture of nonautocrine, factor independent (FI) variant clonal lines of FDCP-1 or bg/bg cl 1 cells was increased over 1000-fold by 15 weeks cocultivation with irradiated stromal cell cultures. FI subclonal lines formed tumors in syngeneic mice and contained no detectable poly A messenger RNA for GM-CSF or IL-3, and no elevation in c-myc, c-abl, c-src, or erb-B onc gene-specific messenger RNA compared to parent factor-dependent lines. These data indicate that x-irradiated plateau phase marrow stromal cells produce increased levels of cell contact-mediated biologically active hemopoietin(s) other than M-CSF, GM-CSF, or IL-3 and induce nonautocrine factor-independent malignant cell lines in vitro.
我们研究了来自C3H/HeJ骨髓的克隆骨髓基质细胞系(称为D2XRII和克隆11)经X射线照射的平台期培养物中造血因子的产生。通过在覆盖新鲜骨髓、IL-3依赖细胞系32D cl 3或GM-CSF/IL-3依赖细胞系FDCP-1或bg/bg cl 1中诱导集落,对对照或10000拉德照射的基质培养物的琼脂覆盖层中CSF的产生进行定量。通过使用新鲜骨髓细胞的生物测定法检测条件培养基中的CSF,通过放射免疫测定法检测M-CSF(CSF-1),并分别通过使用32D cl 3和FDCP-1细胞的微孔增殖测定法检测IL-3和GM-CSF。X射线照射至使CSF-1降至对照水平的40%(大于5000拉德)的剂量,导致FDCP-1或bg/bg cl 1细胞在液体共培养或琼脂培养覆盖层中的生长增加30倍,而32D cl 3未检测到生长。与照射的基质细胞培养物共培养15周后,FDCP-1或bg/bg cl 1细胞的非自分泌、因子非依赖(FI)变异克隆系的传代频率增加了1000倍以上。FI亚克隆系在同基因小鼠中形成肿瘤,与亲本因子依赖系相比,未检测到GM-CSF或IL-3的多聚A信使RNA,且c-myc、c-abl、c-src或erb-B癌基因特异性信使RNA没有升高。这些数据表明,经X射线照射的平台期骨髓基质细胞产生除M-CSF、GM-CSF或IL-3之外的细胞接触介导的生物活性造血因子水平增加,并在体外诱导非自分泌因子非依赖的恶性细胞系。