The role of basic fibroblast growth factor in peripheral nerve regeneration
- PMID: 11681796
- DOI: 10.1007/s004290100205
The role of basic fibroblast growth factor in peripheral nerve regeneration
Abstract
In the peripheral nervous system regeneration and gradual functional restoration occur following peripheral nerve injury. Growth of regenerating axons depends on the presence of diffusible neurotrophic factors, in addition to the substratum. Neurotrophic factors that are involved in peripheral nerve regeneration include nerve growth factor, brain-derived neurotrophic factor, ciliary neurotrophic factor, glial cell line-derived neurotrophic factor, and interleukin-6. Recent functional and expression studies of basic fibroblast growth factor and its receptors have emphasized a physiological role of these molecules in the peripheral nervous system. Basic fibroblast growth factor and its receptors are constitutively expressed in dorsal root ganglia and the peripheral nerve. These molecules display an upregulation in dorsal root ganglia and in the proximal and distal nerve stumps following peripheral nerve injury. In the ganglia these molecules show a mainly neuronal expression, whereas at the lesion site of the nerve, Schwann cells and invading macrophages represent the main cellular sources of basic fibroblast growth factor and the receptors 1-3. Exogenously applied basic fibroblast growth factor mediates rescue effects on injured sensory neurons and supports neurite outgrowth of transectioned nerves. Regarding the expression patterm and the effects after exogenous administration of basic fibroblast growth factor, this molecule seems to play a physiological role during nerve regeneration. Thus, basic fibroblast growth factor could be a promising candidate to contribute to the development of new therapeutic strategies for the treatment of peripheral nerve injuries.
Similar articles
-
Physiological function and putative therapeutic impact of the FGF-2 system in peripheral nerve regeneration--lessons from in vivo studies in mice and rats.Brain Res Rev. 2006 Aug;51(2):293-9. doi: 10.1016/j.brainresrev.2005.12.001. Epub 2006 Jan 23. Brain Res Rev. 2006. PMID: 16430964 Review.
-
In vivo expression and localization of the fibroblast growth factor system in the intact and lesioned rat peripheral nerve and spinal ganglia.J Comp Neurol. 2001 Jun 4;434(3):342-57. doi: 10.1002/cne.1181. J Comp Neurol. 2001. PMID: 11331533
-
The role of neurotrophic factors in nerve regeneration.Neurosurg Focus. 2009 Feb;26(2):E3. doi: 10.3171/FOC.2009.26.2.E3. Neurosurg Focus. 2009. PMID: 19228105 Review.
-
Expression of fibroblast growth factor-2 and fibroblast growth factor receptor 1 messenger RNAs in spinal ganglia and sciatic nerve: regulation after peripheral nerve lesion.Neuroscience. 1997 Jan;76(1):123-35. doi: 10.1016/s0306-4522(96)00355-7. Neuroscience. 1997. PMID: 8971765
-
Faster nerve regeneration after sciatic nerve injury in mice over-expressing basic fibroblast growth factor.J Neurobiol. 2006 Aug;66(9):940-8. doi: 10.1002/neu.20265. J Neurobiol. 2006. PMID: 16758491
Cited by
-
The role of neurotrophic factors conjugated to iron oxide nanoparticles in peripheral nerve regeneration: in vitro studies.Biomed Res Int. 2014;2014:267808. doi: 10.1155/2014/267808. Epub 2014 Jul 16. Biomed Res Int. 2014. PMID: 25133160 Free PMC article.
-
Induction of Id-1 by FGF-2 involves activity of EGR-1 and sensitizes neuroblastoma cells to cell death.J Cell Physiol. 2011 Jul;226(7):1763-70. doi: 10.1002/jcp.22505. J Cell Physiol. 2011. PMID: 21506108 Free PMC article.
-
Spinal astrocytic FGFR3 activation leads to mechanical hypersensitivity by increased TNF-α in spared nerve injury.Int J Clin Exp Pathol. 2019 Aug 1;12(8):2898-2908. eCollection 2019. Int J Clin Exp Pathol. 2019. PMID: 31934126 Free PMC article.
-
Defining a mechanistic link between pigment epithelium-derived factor, docosahexaenoic acid, and corneal nerve regeneration.J Biol Chem. 2017 Nov 10;292(45):18486-18499. doi: 10.1074/jbc.M117.801472. Epub 2017 Sep 26. J Biol Chem. 2017. PMID: 28972155 Free PMC article.
-
STAU1 selectively regulates the expression of inflammatory and immune response genes and alternative splicing of the nerve growth factor receptor signaling pathway.Oncol Rep. 2020 Nov;44(5):1863-1874. doi: 10.3892/or.2020.7769. Epub 2020 Sep 16. Oncol Rep. 2020. PMID: 33000283 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources