Gogusev J, Barbey S, Nezelof C
Unite Inserm 90, Hospital Necker-Enfants Malades, Paris, France.
Anticancer Res. 1993 Jul-Aug;13(4):1043-7.
Following exposure to phorbol ester (TPA), DEL cell line, a human malignant histiocytosis (MH) cell line, is able to differentiate along a macrophage phenotype and thus it provides a suitable model for analyzing the sequential and differential gene expression associated with monocyte/macrophage differentiation. C-myc, c-myb, c-fos, c-sis and c-fms expression were determined by Northern analysis at various times following TPA treatment. The results showed that TPA down-modulated the constitutive expression of c-myc, c-myb, and c-fms, mRNA to low but still detectable levels. Conversely, TPA-induced differentiation resulted in transient appearance of c-fos, whereas no change in the level of c-sis and actin transcripts were observed. Thus, the c-fms and c-sis genes appear to be regulated in a specific manner in this malignant histiocytosis derived cell line. Furthermore, these investigations demonstrated a constitutive CSF-1 gene expression which transiently increased at mRNA and also at protein level as evaluated by a murine bone marrow CFU bioassay. Through this drug-induced modulation, the DEL cell line offers an additional model for studying some of the subtle interrelations existing between a growth factor (CSF-1) and its receptor (c-fms) in the monocyte/macrophage system.
暴露于佛波酯(TPA)后,人恶性组织细胞增多症(MH)细胞系DEL细胞系能够沿着巨噬细胞表型分化,因此它为分析与单核细胞/巨噬细胞分化相关的序列和差异基因表达提供了一个合适的模型。在TPA处理后的不同时间,通过Northern分析确定C-myc、c-myb、c-fos、c-sis和c-fms的表达。结果表明,TPA将c-myc、c-myb和c-fms mRNA的组成型表达下调至低但仍可检测的水平。相反,TPA诱导的分化导致c-fos短暂出现,而c-sis和肌动蛋白转录本水平未观察到变化。因此,在这种源自恶性组织细胞增多症的细胞系中,c-fms和c-sis基因似乎以特定方式受到调控。此外,这些研究表明存在组成型CSF-1基因表达,通过小鼠骨髓CFU生物测定评估,其在mRNA水平以及蛋白质水平均短暂增加。通过这种药物诱导的调节,DEL细胞系为研究单核细胞/巨噬细胞系统中生长因子(CSF-1)及其受体(c-fms)之间存在的一些微妙相互关系提供了另一个模型。