Basic fibroblast growth factor: a potential regulator of proliferation and intermediate filament expression in the retina

• Published in: The Journal of neuroscience 1992-10, Vol.12 (10), p.3968-3978
• Main Authors: Lewis, GP, Erickson, PA, Guerin, CJ, Anderson, DH, Fisher, SK
• Format: Article
• Language: English
• Subjects: Animals; Cats; Cell Division - drug effects; Fibroblast Growth Factor 2 - pharmacology; Intermediate Filaments - metabolism; Rabbits; Retina - cytology; Retina - metabolism
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.12-10-03968.1992

Proliferation of astrocytes, and a concomitant increase of intermediate filaments in astrocytes are two fundamental responses of the CNS to injury. We have previously identified these two events in the retina's response to detachment of the neural retina from the adjoining monolayer of retinal pigmented epithelium. In order to analyze the potential role of basic fibroblast growth factor (bFGF) in these responses, we studied cellular proliferation and intermediate filament protein expression in the retinas of cats and rabbits 4 d and 4 weeks after a single intravitreal injection of 1 microgram of bFGF. Our results show that bFGF stimulates both of these processes in an otherwise normal eye. The eyes that received bFGF had significantly elevated numbers of 3H-thymidine-labeled Müller cells, astrocytes, vascular cells, retinal pigmented epithelial cells, microglia, and macrophages by comparison to control eyes. This proliferation was apparent at 4 d after the injection of bFGF but not after 4 weeks. In control eyes, antibodies to glial fibrillary acidic protein and vimentin labeled intermediate filaments only in the inner (vitread) portion of the Müller cells, the specialized radial astrocytes that span the width of the retina. In eyes that had been injected with bFGF, almost the entire Müller cell cytoplasm was labeled at 4 d after injection; after 4 weeks, the cytoplasmic labeling intensity had increased significantly. Release or activation of endogenous stores of bFGF after injury or disease may be involved in the control of cellular proliferation and intermediate filament expression in the retina and elsewhere in the CNS.