Department of Neurochemistry, Institute of Neurology, London WC1, UK.
EMBO J. 1986 Dec 20;5(13):3449-53. doi: 10.1002/j.1460-2075.1986.tb04668.x.
The effect of nerve growth factor (NGF) on the expression of neurofilament and Thy-1 genes in rat PC12 pheochromocytoma cells was examined at both the transcriptional and post-transcriptional levels. Addition of NGF to cultured PC12 cells produced increases in mRNAs corresponding to the 68 kd neurofilament protein (NF68) and the Thy-1 glycoprotein within 24 h, with maximal effects of some 90- and 45-fold stimulation (relative to beta-actin mRNA) being observed after 12 and 4 days of treatment, respectively. In addition, transcriptional run-off analyses using isolated nuclei showed that NGF treatment resulted directly in 8- and 4-fold increases in the rate of NF68 and Thy-1 gene transcription. These gene activation events were independent of overt morphological differentiation of PC12 cells occurring both under conditions permissive and non-permissive for neurite outgrowth, and once established the new molecular phenotype was dependent upon the continued presence of NGF. This is the first molecular evidence for the reversible activation of neuron-specific genes during NGF-induced differentiation in PC12 cells.
神经生长因子(NGF)对大鼠 PC12 嗜铬细胞瘤细胞中神经丝和 Thy-1 基因表达的影响在转录和转录后水平上进行了研究。在培养的 PC12 细胞中加入 NGF 后,在 24 小时内产生了与 68 kd 神经丝蛋白(NF68)和 Thy-1 糖蛋白相对应的 mRNA 增加,分别在 12 天和 4 天的治疗后观察到最大效应约为 90 倍和 45 倍的刺激(相对于β-肌动蛋白 mRNA)。此外,使用分离的核进行的转录终止分析表明,NGF 处理直接导致 NF68 和 Thy-1 基因转录的速率分别增加 8 倍和 4 倍。这些基因激活事件与允许和不允许神经突生长的条件下 PC12 细胞发生的明显形态分化无关,一旦建立,新的分子表型依赖于 NGF 的持续存在。这是在 NGF 诱导的 PC12 细胞分化过程中神经元特异性基因可逆激活的第一个分子证据。