肌萎缩性侧索硬化症选择性运动神经元死亡的原因和机制。

L Van den Bosch
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引用次数: 0

摘要

肌萎缩性侧索硬化症是一种神经退行性疾病,其特征是运动皮质、脑干和脊髓中的运动神经元选择性死亡。尽管在一些家族性ALS病例中发现了超氧化物歧化酶1 (SOD1)基因突变,但在大多数情况下,ALS的病因尚不清楚。选择性运动神经元死亡的机制尚不清楚。然而,很明显,兴奋性毒性可能在运动神经元死亡的选择性中起作用。兴奋性毒性是指谷氨酸介导的神经元间的正常通讯受到干扰并最终导致神经元死亡的现象。在本研究的第一部分,我们研究了运动神经元的内在特征,这些特征可能是导致这些细胞对兴奋性毒性极其敏感的原因。尽管在ALS中只有运动神经元死亡,但很明显,其他类型的细胞在这一过程中也起着重要作用。在本研究的第二部分,我们集中研究了小胶质细胞的潜在作用。这些细胞是大脑的巨噬细胞,它们在炎症期间被激活。使用二甲胺四环素,我们抑制了小胶质细胞的激活,我们已经研究了它对疾病开始的影响以及对ALS小鼠模型的生存的影响。此外,我们还研究了二甲胺四环素作用的细胞机制。这项研究的目的是深入了解ALS期间选择性运动神经元死亡的机制,我们希望这些信息可以帮助开发治疗这种严重和无法治愈的疾病的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The causes and mechanism of selective motor neuron death in amyotrophic lateral sclerosis].

Amyotrophic lateral sclerosis is a neurodegenerative disease characterized by the selective death of motor neurons in the motor cortex, brain stem and spinal cord. In most cases, the cause of ALS is unknown although in a number of familial ALS cases mutations in the superoxide dismutase 1 (SOD1) gene were discovered. The mechanism underlying the selective motor neuron death is not yet clarified. However, it is clear that excitotoxicity could play a role in the selectivity of the motor neuron death. Excitotoxicity is the phenomenon in which the normal glutamate-mediated communication between neurons is disturbed and ultimately leads to neuronal death. In the first part of this study, we have investigated the intrinsic characteristics of motor neurons that could be responsible for the fact that these cells are extremely sensitive to excitotoxicity. Despite the fact that only the motor neurons die during ALS, it is clear that also other cell types play an important role during this process. In the second part of this study, we have concentrated on the potential role of the microglia. These cells are the macrophages of the brain and they become activated during inflammation. Using minocycline, we have inhibited the activation of the microglia and we have investigated its effect on the start of the disease and on the survival of a mouse model for ALS. Furthermore, we have investigated the cellular mechanism underlying the effect of minocycline. The goal of this research is to get insight into the mechanisms responsible for the selective motor neuron death during ALS and we hope that this information can help in the development of a therapy for this dramatic and incurable disease.

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