Article
Role of NR2B-type NMDA receptors in selective neurodegeneration in Huntington disease.
Neurobiology of aging - 1 Dec 2003
Li Lijun, Fan Mannie, Icton Carolyn D, Chen Nansheng, Leavitt Blair R, Hayden Michael R, Murphy Tim H, Raymond Lynn A
Abstract excerpt
N-Methyl-D-aspartate receptor (NMDAR)-mediated excitotoxicity has been proposed to play a role in Huntington disease (HD), caused by expansion of a polyglutamine tract in the protein huntingtin. HD is characterized by selective neurodegeneration most severely affecting striatal medium-sized spiny projection neurons (MSNs), where expression of the NMDAR subunit NR2B is increased relative to other NR2 subunits....
Topics
- Animals
- Cells, Cultured
- Disease Models, Animal
- Genetic Predisposition to Disease
- Huntingtin Protein
- Huntington Disease
- Membrane Potentials
- Mice
- Mice, Transgenic
- Mutation
- Neostriatum
