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Decreased expression of GLT ‐1 in the R6/2 model of Huntington's disease does not worsen disease progression
Author(s) -
Petr Geraldine T.,
Schultheis Laurel A.,
Hussey Kayla C.,
Sun Yan,
Dubinsky Janet M.,
Aoki Chiye,
Rosenberg Paul A.
Publication year - 2013
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/ejn.12202
Subject(s) - striatum , glutamate receptor , excitotoxicity , biology , huntington's disease , glutamatergic , genetically modified mouse , endocrinology , transgene , medicine , neuroscience , dopamine , receptor , biochemistry , gene , disease
Excitotoxicity is thought to be important in the pathogenesis of Huntington's disease ( HD ). Glutamate is the predominant excitatory neurotransmitter in the brain, and excess activation of glutamate receptors can cause neuronal dysfunction and death. Glutamate transporters regulate the extracellular concentration of glutamate. GLT ‐1 is the most abundant glutamate transporter, and accounts for most of the glutamate transport in the brain. Administration of ceftriaxone, an antibiotic that increases the functional expression of GLT ‐1, can improve the behavioral phenotype of the R6/2 mouse model of HD . To test the hypothesis that GLT ‐1 expression critically affects the HD disease process, we generated a novel mouse model that is heterozygous for the null allele of GLT ‐1 and carries the R6/2 transgene (double mutation). We demonstrated that the protein expression of total GLT ‐1, as well as two of its isoforms, is decreased within the cortex and striatum of 12‐week‐old R6/2 mice, and that the expression of EAAC 1 was decreased in the striatum. Protein expression of GLT ‐1 was further decreased in the cortex and striatum of the double mutation mice compared with the R6/2 mice at 11 weeks. However, the effects of the R6/2 transgene on weight loss, accelerating rotarod, climbing and paw‐clasping were not exacerbated in these double mutants. Na + ‐dependent glutamate uptake into synapatosomes isolated from the striatum and cortex of 11‐week‐old R6/2 mice was unchanged compared with controls. These results suggest that changes in GLT ‐1 expression or function per se are unlikely to potentiate or ameliorate the progression of HD .