Rydel R E, Greene L A
Department of Pharmacology, New York University School of Medicine, New York 10016.
J Neurosci. 1987 Nov;7(11):3639-53. doi: 10.1523/JNEUROSCI.07-11-03639.1987.
Acidic (aFGF) and basic (bFGF) fibroblast growth factors are well-characterized peptide hormones that have potent angiogenic activity and that are mitogenic for a variety of cell types. The present findings demonstrate that FGFs can reproduce the entire spectrum of rat pheochromocytoma PC12 cell responses previously shown to be elicited by NGF. These include responses that are rapid (cell flattening, enhanced phosphorylation of tyrosine hydroxylase) or delayed (neurite outgrowth, induction of phosphorylated MAP 1.2, regulation of NILE and Thy-1 glycoproteins, cessation of mitosis, elevation of AChE activity), as well as responses that have been shown to be either transcription-independent (neurite regeneration, promotion of survival) or transcription-dependent (priming, regulation of NILE and Thy-1 glycoproteins, elevation of AChE activity). The only responses for which the FGFs and NGF consistently showed quantitative differences were in the rates for neurite initiation and elongation in serum-containing medium. Thus, while all 3 factors promoted the formation of stable neurites, the network of outgrowth elicited by NGF at any given time of treatment was always of greater density. Togari et al. (1985) have previously reported that bFGF can initiate transient neurite formation in PC12 cell cultures. The present observations describe a variety of additional actions of bFGF on a neuronal cell line, and demonstrate that aFGF is capable of mimicking many, if not all, of these actions. These observations thus extend the range of actions that aFGF and bFGF may potentially exert on nerve cells, either during their development, repair, or maintenance. In addition, this work suggests that the PC12 cell line may serve as a useful model system with which to study the mechanism of action of FGFs on neurons. Since all 3 factors appear capable of eliciting the same wide spectrum of responses, molecular events specifically associated with FGFs and NGF in PC12 cells may prove illuminating of the causal steps involved in neuronal differentiation.
酸性(aFGF)和碱性(bFGF)成纤维细胞生长因子是特性明确的肽类激素,具有强大的血管生成活性,对多种细胞类型具有促有丝分裂活性。目前的研究结果表明,FGFs能够重现先前显示由NGF引发的大鼠嗜铬细胞瘤PC12细胞反应的整个范围。这些反应包括快速反应(细胞变平、酪氨酸羟化酶磷酸化增强)或延迟反应(神经突生长、磷酸化MAP 1.2的诱导、NILE和Thy-1糖蛋白的调节、有丝分裂停止、乙酰胆碱酯酶活性升高),以及已显示为不依赖转录(神经突再生、促进存活)或依赖转录(启动、NILE和Thy-1糖蛋白的调节、乙酰胆碱酯酶活性升高)的反应。FGFs和NGF始终表现出定量差异的唯一反应是在含血清培养基中神经突起始和伸长的速率。因此,虽然所有这3种因子都促进了稳定神经突的形成,但在任何给定的处理时间,由NGF引发的生长网络总是密度更大。Togari等人(1985年)先前报道,bFGF可以在PC12细胞培养物中引发短暂的神经突形成。目前的观察结果描述了bFGF对神经元细胞系的多种额外作用,并证明aFGF能够模拟其中许多(如果不是全部)作用。因此,这些观察结果扩展了aFGF和bFGF在神经细胞发育、修复或维持过程中可能潜在发挥作用的范围。此外,这项工作表明PC12细胞系可能是一个有用的模型系统,用于研究FGFs对神经元的作用机制。由于所有这3种因子似乎都能够引发相同广泛的反应,PC12细胞中与FGFs和NGF特异性相关的分子事件可能有助于阐明神经元分化所涉及的因果步骤。