Synergistic effect of GDNF and NGF on axonal branching and elongation in vitro
Neuroscience Research, ISSN: 0168-0102, Vol: 65, Issue: 1, Page: 88-97
2009
- 118Citations
- 82Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations118
- Citation Indexes118
- 118
- CrossRef88
- Captures82
- Readers82
- 82
Article Description
There is a clinical need to enhance functional recovery of injured peripheral nerves. Local administration of neurotrophic factors (NTFs) after surgical repair has been proposed for this purpose. Little is known, however, on the optimal local dose and dosing frequency of NTFs in a peripheral nerve defect. For increasing our knowledge on biologically relevant local NTFs concentrations and for making available an in vitro assay for assessing the bioactivity of NTFs in connection with implantable localized delivery systems, we developed in this study a bioassay for NTFs, which is based on dorsal root ganglion (DRG) explants from E9 (9 days old) chicken embryos. Axonal elongation and extent of axonal branching was analyzed microscopically after addition of glial cell line-derived neurotrophic factor (GDNF) and nerve growth factor (NGF), each alone and in combination. GDNF significantly promoted axonal elongation, but only little axonal branching, whereas NGF induced extensive axonal branching with modest axonal elongation. The combination of GDNF and NGF exerted a synergistic effect on the axonal elongation, axonal branching and growth kinetics. GDNF and NGF also enhanced the expression of their respective functional receptors Ret and TrkA on the DRG neurons. This information should be relevant for the development of implants containing NTFs and on drug therapy of damaged peripheral nerves.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0168010209001783; http://dx.doi.org/10.1016/j.neures.2009.06.003; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=67650617681&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/19523996; https://linkinghub.elsevier.com/retrieve/pii/S0168010209001783; https://dx.doi.org/10.1016/j.neures.2009.06.003
Elsevier BV
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