Acidic and basic fibroblast growth factors promote stable neurite outgrowth and neuronal differentiation in cultures of PC12 cells
Open Access
- 1 November 1987
- journal article
- research article
- Published by Society for Neuroscience in Journal of Neuroscience
- Vol. 7 (11), 3639-3653
- https://doi.org/10.1523/jneurosci.07-11-03639.1987
Abstract
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.This publication has 34 references indexed in Scilit:
- PC12 Pheochromocytoma Cultures in Neurobiological ResearchPublished by Elsevier ,1982
- Regulation of acetylcholinesterase by nerve growth factor in the pheochromocytoma PC12 cell lineNeuroscience Letters, 1980
- The effects of nerve growth factor on acetylcholinesterase and its multiple forms in cultures of rat PC12 pheochromocytoma cells: Increased total specific activity and appearance of the 16 S molecular formDevelopmental Biology, 1980
- Identification with cellular microtubules of one of the co-assembling microtubule-associated proteinsCell, 1979
- Induction of fibre outgrowth and choline acetyltransferase in PC12 pheochromocytoma cells by conditioned media from glial cells and organ extractsExperimental Cell Research, 1979
- Evidence for RNA synthesis-dependent and -independent pathways in stimulation of neurite outgrowth by nerve growth factorProceedings of the National Academy of Sciences, 1978
- NGF stimulates incorporation of fucose or glucosamine into an external glycoprotein in cultured rat PC12 pheochromocytoma cellsCell, 1978
- Nerve growth factor prevents the death and stimulates the neuronal differentiation of clonal PC12 pheochromocytoma cells in serum-free mediumThe Journal of cell biology, 1978
- Characterization and isolation of proteolytically modified nerve growth factorBiochemistry, 1976
- Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor.Proceedings of the National Academy of Sciences, 1976