Inflammation-induced GDNF improves locomotor function after spinal cord injury
- PMID: 15671854
- DOI: 10.1097/00001756-200502080-00004
Inflammation-induced GDNF improves locomotor function after spinal cord injury
Abstract
Activation of microglia/macrophages after injury occurs limitedly in the CNS, which finding may explain unsuccessful axonal regeneration. Therefore, the relationship between lipopolysaccharide (LPS)-induced inflammation and recovery of locomotor function of rats after spinal cord injury was examined. High-dose LPS improved locomotor function greater than low-dose LPS, being consistent with the expression of neurotrophic factor (GDNF) in microglia/macrophages. Experiments using GDNF gene mutant mice confirmed that the increase in the GDNF mRNA level, rather than the reduction in the mRNA level of inducible NO synthase, could be correlated with the restoration activity of locomotor function. These results suggest that a higher degree of inflammation leads to a higher degree of repair of CNS injuries through GDNF produced by activated microglia/macrophages.
Similar articles
-
Involvement of glial cell line-derived neurotrophic factor in activation processes of rodent macrophages.J Neurosci Res. 2005 Feb 15;79(4):476-87. doi: 10.1002/jnr.20368. J Neurosci Res. 2005. PMID: 15635609
-
Stimulation of production of glial cell line-derived neurotrophic factor and nitric oxide by lipopolysaccharide with different dose-responsiveness in cultured rat macrophages.Biomed Res. 2005 Oct;26(5):223-9. doi: 10.2220/biomedres.26.223. Biomed Res. 2005. PMID: 16295699
-
Cationic liposome-mediated GDNF gene transfer after spinal cord injury.J Neurotrauma. 2002 Sep;19(9):1081-90. doi: 10.1089/089771502760341983. J Neurotrauma. 2002. PMID: 12482120
-
Regulation of microglial activities by glial cell line derived neurotrophic factor.J Cell Biochem. 2006 Feb 15;97(3):501-11. doi: 10.1002/jcb.20646. J Cell Biochem. 2006. PMID: 16187294
-
New approaches for the treatment of pain: the GDNF family of neurotrophic growth factors.Curr Top Med Chem. 2005;5(6):577-83. doi: 10.2174/1568026054367593. Curr Top Med Chem. 2005. PMID: 16022680 Review.
Cited by
-
Osteopontin-deficient mice exhibit less inflammation, greater tissue damage, and impaired locomotor recovery from spinal cord injury compared with wild-type controls.J Neurosci. 2007 Mar 28;27(13):3603-11. doi: 10.1523/JNEUROSCI.4805-06.2007. J Neurosci. 2007. PMID: 17392476 Free PMC article.
-
Expression of neurotrophin and its tropomyosin-related kinase receptors (Trks) during axonal regeneration following spinal cord injury in larval lamprey.Neuroscience. 2011 Jun 2;183:265-77. doi: 10.1016/j.neuroscience.2011.03.024. Epub 2011 Mar 21. Neuroscience. 2011. PMID: 21421025 Free PMC article.
-
The Function of FGFR1 Signalling in the Spinal Cord: Therapeutic Approaches Using FGFR1 Ligands after Spinal Cord Injury.Neural Plast. 2017;2017:2740768. doi: 10.1155/2017/2740768. Epub 2017 Jan 18. Neural Plast. 2017. PMID: 28197342 Free PMC article. Review.
-
Low-Dose LPS Modulates Microglia/Macrophages Phenotypic Transformation to Amplify Rehabilitation Effects in Chronic Spinal Cord Injured (CSCI) Mice.Mol Neurobiol. 2024 Sep;61(9):6484-6500. doi: 10.1007/s12035-024-03979-y. Epub 2024 Feb 5. Mol Neurobiol. 2024. PMID: 38311654
-
GDNF, A Neuron-Derived Factor Upregulated in Glial Cells during Disease.J Clin Med. 2020 Feb 7;9(2):456. doi: 10.3390/jcm9020456. J Clin Med. 2020. PMID: 32046031 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases