Kolber A R, Goldstein M N, Moore B W
Proc Natl Acad Sci U S A. 1974 Oct;71(10):4203-7. doi: 10.1073/pnas.71.10.4203.
Purified nerve growth factor induced the outgrowth of neurites from cultured human neuroblastoma cells (NJB line) and a concomitant increase in colchicine-binding activity in extracts from these cultures. The parallel stimulation of neurite outgrowth from the cells and colchicine-binding activity of the extracts is interpreted to represent de novo synthesis of microtubular subunit protein in response to the challenge by nerve growth factor. The regulation of the expression of 14-3-2 protein, a protein characteristic of differentiated neuronal cells, was not affected in NJB cells by the addition of nerve growth factor to the culture medium. 14-3-2 protein is present in NJB cells at a concentration equal to that present in human brain from subculture to the stationary phase of growth of the tumor cells. It was concluded that these two gene products, characteristic of differentiated neural cells, are not coordinately regulated in NJB human neuroblastoma cells.
纯化的神经生长因子可诱导培养的人神经母细胞瘤细胞(NJB系)长出神经突,并使这些培养物提取物中的秋水仙碱结合活性随之增加。细胞神经突生长与提取物秋水仙碱结合活性的平行刺激被解释为,这代表了响应神经生长因子的刺激而从头合成微管亚基蛋白。向培养基中添加神经生长因子,并不会影响NJB细胞中14-3-2蛋白(一种分化神经元细胞特有的蛋白)表达的调节。从传代培养到肿瘤细胞生长的静止期,NJB细胞中14-3-2蛋白的浓度与人脑中该蛋白的浓度相当。得出的结论是,这两种分化神经细胞特有的基因产物在NJB人神经母细胞瘤细胞中不受协同调节。