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神经生长因子对c-Fos和Zif268蛋白的合成、磷酸化及DNA结合活性的正常刺激不足以介导PC12细胞的神经元分化。

Normal stimulation of the synthesis, phosphorylation and DNA binding activity of c-Fos and Zif268 proteins by nerve growth factor is not sufficient to mediate neuronal differentiation of PC12 cells.

作者信息

Szeberényi J

机构信息

Department of Medical Biology, University Medical Biology, University Medical School of Pécs, Hungary.

出版信息

Mol Cell Biochem. 1998 Dec;189(1-2):71-7. doi: 10.1023/a:1006813501633.

Abstract

Early-response genes (ERGs) are rapidly induced by nerve growth factor (NGF) in the PC12 rat pheochromocytoma cell line. To analyze the possible role of Ras and ERGs in neuronal differentiation, experiments were carried out to study the involvement of Ras proteins in the NGF-stimulated expression of two ERG-coded proteins (c-Fos and Zif268) implicated in NGF signaling. Using PC12 subclones expressing the dominant negative Ha-Ras Asn-17 protein, NGF-induced expression, phosphorylation and DNA-binding of these ERG products were found to be not sufficient to convey the biological response of PC12 cells to NGF.

摘要

早期反应基因(ERGs)在PC12大鼠嗜铬细胞瘤细胞系中可被神经生长因子(NGF)迅速诱导。为了分析Ras和ERGs在神经元分化中的可能作用,开展了实验以研究Ras蛋白在NGF刺激的两种参与NGF信号传导的ERG编码蛋白(c-Fos和Zif268)表达中的作用。使用表达显性负性Ha-Ras Asn-17蛋白的PC12亚克隆,发现这些ERG产物的NGF诱导表达、磷酸化和DNA结合不足以传达PC12细胞对NGF的生物学反应。

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