Abstract
Deficient RNA editing of the AMPA receptor subunit GluR2 at the Q/R site is a primary cause of neuronal death and recently has been reported to be a tightly linked etiological cause of motor neuron death in sporadic amyotrophic lateral sclerosis (ALS). We quantified the RNA editing efficiency of the GluR2 Q/R site in single motor neurons of rats transgenic for mutant human Cu/Zn-superoxide dismutase (SOD1) as well as patients with spinal and bulbar muscular atrophy (SBMA), and found that GluR2 mRNA was completely edited in all the motor neurons examined. It seems likely that the death cascade is different among the dying motor neurons in sporadic ALS, familial ALS with mutant SOD1 and SBMA.
Original language | English |
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Pages (from-to) | 11-14 |
Number of pages | 4 |
Journal | Neuroscience Research |
Volume | 54 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2006 Jan |
Keywords
- ALS
- AMPA receptor
- GluR2
- Motor neuron
- Neuronal death
- RNA editing
- SOD1
- Spinal and bulbar muscular atrophy
ASJC Scopus subject areas
- Neuroscience(all)