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通过与经辐照的骨髓基质细胞系共培养诱导因子依赖性造血祖细胞系中的生长改变。

Induction of growth alterations in factor-dependent hematopoietic progenitor cell lines by cocultivation with irradiated bone marrow stromal cell lines.

作者信息

Naparstek E, Pierce J, Metcalf D, Shadduck R, Ihle J, Leder A, Sakakeeny M A, Wagner K, Falco J, FitzGerald T J

出版信息

Blood. 1986 May;67(5):1395-403.

PMID:2870752
Abstract

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.

摘要

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。

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