Sugimoto T, Umezawa A, Hata J
Department of Pathology, Keio University School of Medicine, Tokyo, Japan.
Virchows Arch. 1997 Jan;430(1):41-6. doi: 10.1007/BF01008015.
We investigated the capacity of eight well-characterized Ewing's sarcoma cell lines to differentiate towards a neural phenotype. Ewing's sarcoma cells expressed the neuroectoderm-associated antigens such as nerve growth factor (NGF) receptor, N-CAM (6H7 and Leu-19) and Leu-7. Ewing's sarcoma cells also exhibited the potential for neural differentiation at the mRNA level; neuron-specific medium- and low-sized filament (NF-M and NF-L) expression was induced by dibutyryladenosine cyclic monophosphate. The pattern of expression of NF-L obtained by using alternative polyadenylation sites in Ewing's sarcoma cells differed from that in peripheral primitive neuroectodermal tumour (PNET) cells, and was similar to that in undifferentiated neural tissues. Furthermore, the NGF receptors detected by immunohistochemistry were found to be non-functional as assayed by c-fos induction with NGF treatment. The results indicate that Ewing's sarcoma cells maintain a primitive phenotype and have the potential to differentiate into a neural phenotype, indicating that Ewing's sarcoma is distinct from PNET.
我们研究了八种特征明确的尤因肉瘤细胞系向神经表型分化的能力。尤因肉瘤细胞表达神经外胚层相关抗原,如神经生长因子(NGF)受体、N-CAM(6H7和Leu-19)以及Leu-7。尤因肉瘤细胞在mRNA水平也表现出神经分化的潜力;二丁酰腺苷环化一磷酸可诱导神经元特异性中、低分子量细丝(NF-M和NF-L)的表达。在尤因肉瘤细胞中,通过使用可变聚腺苷酸化位点获得的NF-L表达模式与外周原始神经外胚层肿瘤(PNET)细胞不同,而与未分化神经组织中的模式相似。此外,通过免疫组织化学检测到的NGF受体经NGF处理诱导c-fos后被发现无功能。结果表明,尤因肉瘤细胞保持原始表型并具有分化为神经表型的潜力,这表明尤因肉瘤与PNET不同。