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Expression of mutant huntingtin in glial cells contributes to neuronal excitotoxicity

Huntington disease (HD) is characterized by the preferential loss of striatal medium-sized spiny neurons (MSNs) in the brain. Because MSNs receive abundant glutamatergic input, their vulnerability to excitotoxicity may be largely influenced by the capacity of glial cells to remove extracellular glut...

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Detalhes bibliográficos
Main Authors: Shin, Ji-Yeon, Fang, Zhi-Hui, Yu, Zhao-Xue, Wang, Chuan-En, Li, Shi-Hua, Li, Xiao-Jiang
Formato: Artigo
Idioma:Inglês
Publicado em: The Rockefeller University Press 2005
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2171327/
https://ncbi.nlm.nih.gov/pubmed/16365166
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.200508072
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