Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice

Article

关键词: AMYOTROPHIC-LATERAL-SCLEROSIS;    FRONTOTEMPORAL LOBAR DEGENERATION;    ANTISENSE OLIGONUCLEOTIDE;    STRESS GRANULES;    ALS;    DISEASE;    RNA;    EXPANSIONS;    FEATURES;    MODELS;   

DOI  :  10.1038/nature22038

来源: SCIE

【 摘 要 】

Amyotrophic lateral sclerosis (ALS) is a rapidly progressing neurodegenerative disease that is characterized by motor neuron loss and that leads to paralysis and death 2-5 years after disease onset(1). Nearly all patients with ALS have aggregates of the RNA-binding protein TDP-43 in their brains and spinal cords(2), and rare mutations in the gene encoding TDP-43 can cause ALS3. There are no effective TDP-43-directed therapies for ALS or related TDP-43 proteinopathies, such as frontotemporal dementia. Antisense oligonucleotides (ASOs) and RNA-interference approaches are emerging as attractive therapeutic strategies in neurological diseases(4). Indeed, treatment of a rat model of inherited ALS (caused by a mutation in Sod1) with ASOs against Sod1 has been shown to substantially slow disease progression(5). However, as SOD1 mutations account for only around 2-5% of ALS cases, additional therapeutic strategies are needed. Silencing TDP-43 itself is probably not appropriate, given its critical cellular functions(1,6). Here we present a promising alternative therapeutic strategy for ALS that involves targeting ataxin-2. A decrease in ataxin-2 suppresses TDP-43 toxicity in yeast and flies(7), and intermediate-length polyglutamine expansions in the ataxin-2 gene increase risk of ALS(7,8). We used two independent approaches to test whether decreasing ataxin-2 levels could mitigate disease in a mouse model of TDP-43 proteinopathy(9). First, we crossed ataxin-2 knockout mice with TDP-43 (also known as TARDBP) transgenic mice. The decrease in ataxin-2 reduced aggregation of TDP-43, markedly increased survival and improved motor function. Second, in a more therapeutically applicable approach, we administered ASOs targeting ataxin-2 to the central nervous system of TDP-43 transgenic mice. This single treatment markedly extended survival. Because TDP-43 aggregation is a component of nearly all cases of ALS6, targeting ataxin-2 could represent a broadly effective therapeutic strategy.

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