Laboratory of Molecular Neuroscience, Medical Research Institute (MRI), Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
Laboratory of Molecular Neuroscience, Medical Research Institute (MRI), Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan; Center for Brain Integration Research (CBIR), TMDU, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
Biochem Biophys Res Commun. 2018 Mar 4;497(2):689-693. doi: 10.1016/j.bbrc.2018.02.132. Epub 2018 Feb 16.
Amyotrophic lateral sclerosis (ALS) is a chronic neurodegenerative disorder characterized by the selective loss of motor neurons. The precise mechanisms that cause the selective death of motor neurons remain unclear, but a growing body of evidence suggests that glutamate-mediated excitotoxicity has been considered to play an important role in the mechanisms of motor neuron degeneration in ALS. Reductions in glutamate transporter GLT1 have been reported in animal models of ALS and the motor cortex and spinal cord of ALS patients. However, it remains unknown whether the reduction in GLT1 has a primary role in the induction of motor neuron degeneration in ALS. Here, we generated conditional knockout mice that lacked GLT1 specifically in the spinal cord by crossing floxed-GLT1 mice and Hoxb8-Cre mice. Hoxb8-Cre/GLT1 mice showed motor deficits and motor neuron loss. Thus, loss of the glial glutamate transporter GLT1 is sufficient to cause motor neuron death in mice.
肌萎缩侧索硬化症(ALS)是一种慢性神经退行性疾病,其特征是运动神经元的选择性丧失。导致运动神经元选择性死亡的确切机制尚不清楚,但越来越多的证据表明,谷氨酸介导的兴奋性毒性被认为在 ALS 中运动神经元退化的机制中起重要作用。在 ALS 的动物模型以及 ALS 患者的运动皮层和脊髓中,已报道谷氨酸转运体 GLT1 减少。然而,GLT1 的减少是否在 ALS 中诱导运动神经元退化中起主要作用仍不清楚。在这里,我们通过将 floxed-GLT1 小鼠与 Hoxb8-Cre 小鼠杂交,生成了脊髓中特异性缺乏 GLT1 的条件敲除小鼠。Hoxb8-Cre/GLT1 小鼠表现出运动功能障碍和运动神经元丧失。因此,胶质谷氨酸转运体 GLT1 的缺失足以导致小鼠运动神经元死亡。