Differential effects of glial cell line-derived neurotrophic factor on A9 and A10 dopamine neuron survival in vitro
Neuroscience, ISSN: 0306-4522, Vol: 147, Issue: 3, Page: 712-719
2007
- 15Citations
- 24Captures
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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
- Citations15
- Citation Indexes15
- 15
- CrossRef14
- Captures24
- Readers24
- 24
Article Description
Glial cell-line derived neurotrophic factor (GDNF) enhances dopamine (DA) cell survival and fiber outgrowth, and may be beneficial in enhancing cell restorative strategies for Parkinson’s disease (PD). However, GDNF may have different roles for transplanted DA cell sub-types. The present in vitro study investigated the effect of GDNF on the survival of rat DA cells displaying a phenotype consistent with either the substantia nigra [A9 cells immunopositive for tyrosine hydroxylase (TH) and G-protein-gated inwardly rectifying potassium channel subunit 2 (GIRK2)] or with the ventral tegmental area [A10 cells immunopositive for TH and calbindin]. It was found that a single exposure of GDNF enhanced the number of DA cells of an A9 phenotype, without affecting DA cells of an A10 phenotype. Conversely, repeated GDNF exposure did not alter the survival of A9 phenotypic cells, but doubled the percentage of A10 cells. It was concluded that GDNF administration may affect dopaminergic cells differently depending on time and degree of GDNF exposure. For cell transplantation in PD, long-term GDNF administration may result in detrimental effects for transplanted A9 TH+ cells as this may introduce competition with A10 TH+ cells for survival and fiber outgrowth into the host striatum. These results may have important implications for clinical neural transplantation in PD.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0306452207004198; http://dx.doi.org/10.1016/j.neuroscience.2007.03.057; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=34347269143&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/17583436; https://linkinghub.elsevier.com/retrieve/pii/S0306452207004198; https://dx.doi.org/10.1016/j.neuroscience.2007.03.057
Elsevier BV
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