BTBD10, an Akt interactor, activates Akt by decreasing the protein phosphatase 2A-mediated dephosphorylation and inactivation of Akt. Overexpression of BTBD10 suppresses motor neuron death that is induced by a familial amyotrophic lateral sclerosis (ALS)-linked superoxide dismutase 1 (SOD1) mutant, G93A-SOD1 in vitro. In this study, we further investigated the BTBD10-mediated suppression of motor neuron death. We found that the small interfering RNA-mediated inhibition of BTBD10 expression led to the death of cultured motor neurons. In Caenorhabditis elegans (C. elegans), disruption of the btbd-10 gene caused not only loss of neurons, including both motor and touch-receptor neurons, but also a locomotion defect. In addition, we found that the expression of BTBD10 was generally decreased in the motor neurons from patients of sporadic ALS and transgenic mice overexpressing G93A-SOD1 (G93A-SOD1-transgenic mice). Collectively, these results suggest that the reduced expression of BTBD10 leads to motor neuron death both in vitro and in vivo.
Reduced expression of BTBD10, an Akt activator, leads to motor neuron death.
Akt 激活因子 BTBD10 表达降低会导致运动神经元死亡
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作者:Nawa M, Kage-Nakadai E, Aiso S, Okamoto K, Mitani S, Matsuoka M
| 期刊: | Cell Death and Differentiation | 影响因子: | 15.400 |
| 时间: | 2012 | 起止号: | 2012 Aug;19(8):1398-407 |
| doi: | 10.1038/cdd.2012.19 | 研究方向: | 神经科学 |
| 信号通路: | PI3K/Akt | ||
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