Acidic and basic fibroblast growth factors in the nervous system: distribution and differential alteration of levels after injury of central versus peripheral nerve
- PMID: 1992009
- PMCID: PMC6575224
- DOI: 10.1523/JNEUROSCI.11-02-00412.1991
Acidic and basic fibroblast growth factors in the nervous system: distribution and differential alteration of levels after injury of central versus peripheral nerve
Abstract
Acidic and basic fibroblast growth factors (aFGF and bFGF) are known to stimulate mitogenesis in a variety of non-neuronal cell types. Recent work has also established that FGFs can act as neurotrophic factors that promote the survival and regeneration in vitro of a variety of neurons. The present study investigates the distribution of aFGF and bFGF in vivo by using a mitogenic bioassay on AKR-2B cells coupled with Western-blot analysis to estimate the levels of aFGF and bFGF in different areas of the rat nervous system. Acidic FGF and bFGF from extracts of nervous tissue were found to differ considerably in their relative dependencies upon heparin to potentiate their mitogenic activities: the effect of aFGF was strongly dependent upon heparin, whereas the effect of bFGF was only slightly potentiated by heparin. Heparin was also found to stimulate differentially the mitogenic activity of extracts prepared from different areas of the nervous system, indicating that spinal cord, cortex, pituitary, and optic nerve contained different ratios of aFGF to bFGF, whereas sciatic nerve contained extremely high levels of only aFGF. These results were confirmed in Western-blot experiments, using antibodies specific for either aFGF or bFGF. Transection of nerves had opposing effects in sciatic and optic nerves: aFGF rapidly declined in the sciatic nerve distal to the cut, whereas bFGF increased slightly in the distal portion of the cut optic nerve. This differential effect of injury on FGF levels in central versus peripheral nerves may reflect the differential regenerative potential of these two types of nerves.
Similar articles
-
Differential localization and possible functions of aFGF and bFGF in the central and peripheral nervous systems.Ann N Y Acad Sci. 1991;638:348-60. doi: 10.1111/j.1749-6632.1991.tb49045.x. Ann N Y Acad Sci. 1991. PMID: 1723856
-
Culture-induced increase in acidic and basic fibroblast growth factor activities and their association with the nuclei of vascular endothelial and smooth muscle cells.J Cell Physiol. 1991 May;147(2):362-73. doi: 10.1002/jcp.1041470223. J Cell Physiol. 1991. PMID: 1710230
-
Developmental time course of acidic and basic fibroblast growth factors' expression in distinct cellular populations of the rat central nervous system.J Comp Neurol. 1995 Jul 17;358(1):142-53. doi: 10.1002/cne.903580109. J Comp Neurol. 1995. PMID: 7560275
-
[Fibroblast growth factors (FGFs) in neurodegenerative disorders].Rinsho Shinkeigaku. 1993 Dec;33(12):1270-4. Rinsho Shinkeigaku. 1993. PMID: 8174323 Review. Japanese.
-
Fibroblast (heparin-binding) growing factors in neuronal development and repair.Mol Neurobiol. 1988 Winter;2(4):263-89. doi: 10.1007/BF02935635. Mol Neurobiol. 1988. PMID: 2855976 Review.
Cited by
-
Alternatives to sural nerve grafts in the upper extremity.Hand (N Y). 2015 Mar;10(1):68-75. doi: 10.1007/s11552-014-9699-6. Hand (N Y). 2015. PMID: 25767423 Free PMC article.
-
Basic fibroblast growth factor in Dupuytren's contracture.Am J Pathol. 1992 Sep;141(3):661-71. Am J Pathol. 1992. PMID: 1325742 Free PMC article.
-
Maintaining the neuronal phenotype after injury in the adult CNS. Neurotrophic factors, axonal growth substrates, and gene therapy.Mol Neurobiol. 1995 Apr-Jun;10(2-3):151-67. doi: 10.1007/BF02740673. Mol Neurobiol. 1995. PMID: 7576305 Review.
-
Effect of basic fibroblast growth factor and cytochrome c peroxidase combination in transgenic mice corneal epithelial healing process after excimer laser photoablation.Clin Ophthalmol. 2011;5:215-21. doi: 10.2147/OPTH.S16866. Epub 2011 Feb 16. Clin Ophthalmol. 2011. PMID: 21386914 Free PMC article.
-
Antidepressant-like effects of trophic factor receptor signaling.Front Mol Neurosci. 2022 Aug 23;15:958797. doi: 10.3389/fnmol.2022.958797. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36081576 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources