Prentice H M, Moore S E, Dickson J G, Doherty P, Walsh F S
Department of Neurochemistry, Institute of Neurology, London, UK.
EMBO J. 1987 Jul;6(7):1859-63. doi: 10.1002/j.1460-2075.1987.tb02444.x.
The effects of nerve growth factor (NGF) on the expression of neural cell adhesion molecule (N-CAM) in PC12 cells were determined. A quantitative immunoassay was used to show that NGF induces a 4- to 5-fold increase in relative N-CAM levels over a 3-day period. This increase could not be mimicked by cholera toxin suggesting that it is not a simple consequence of morphological differentiation. The changes in N-CAM levels induced by NGF were accompanied by changes in N-CAM molecular forms. The 140-kd N-CAM species is the major N-CAM expressed by naive PC12 cells, while NGF-treated cultures express N-CAM species of 180 kd and 140 kd. Northern analysis showed that naive cells express a 6.7-kd N-CAM mRNA species only, while NGF-treated cultures express both a 6.7-kb and a 7.2-kb transcript. As the 6.7-kb and 7.2-kb mRNAs are alternative spliced transcripts of a single gene, this result shows that NGF can activate a neuron-specific splicing mechanism. This is the first description of control of N-CAM expression by a growth factor.
测定了神经生长因子(NGF)对PC12细胞中神经细胞黏附分子(N-CAM)表达的影响。采用定量免疫分析法显示,在3天的时间里,NGF可使相对N-CAM水平增加4至5倍。霍乱毒素无法模拟这种增加,这表明它不是形态分化的简单结果。NGF诱导的N-CAM水平变化伴随着N-CAM分子形式的变化。140-kd的N-CAM是未处理的PC12细胞表达的主要N-CAM,而经NGF处理的培养物表达180 kd和140 kd的N-CAM。Northern分析表明,未处理的细胞仅表达一种6.7-kd的N-CAM mRNA,而经NGF处理的培养物则表达6.7-kb和7.2-kb的转录本。由于6.7-kb和7.2-kb的mRNA是单个基因的可变剪接转录本,这一结果表明NGF可激活神经元特异性剪接机制。这是首次对生长因子控制N-CAM表达的描述。