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基于行为的药物筛选系统,使用秀丽隐杆线虫运动神经元疾病模型。

A behavior-based drug screening system using a Caenorhabditis elegans model of motor neuron disease.

机构信息

Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Department of Neurology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

出版信息

Sci Rep. 2019 Jul 12;9(1):10104. doi: 10.1038/s41598-019-46642-6.

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the progressive loss of motor neurons, for which there is no effective treatment. Previously, we generated a Caenorhabditis elegans model of ALS, in which the expression of dnc-1, the homologous gene of human dynactin-1, is knocked down (KD) specifically in motor neurons. This dnc-1 KD model showed progressive motor defects together with axonal and neuronal degeneration, as observed in ALS patients. In the present study, we established a behavior-based, automated, and quantitative drug screening system using this dnc-1 KD model together with Multi-Worm Tracker (MWT), and tested whether 38 candidate neuroprotective compounds could improve the mobility of the dnc-1 KD animals. We found that 12 compounds, including riluzole, which is an approved medication for ALS patients, ameliorated the phenotype of the dnc-1 KD animals. Nifedipine, a calcium channel blocker, most robustly ameliorated the motor deficits as well as axonal degeneration of dnc-1 KD animals. Nifedipine also ameliorated the motor defects of other motor neuronal degeneration models of C. elegans, including dnc-1 mutants and human TAR DNA-binding protein of 43 kDa overexpressing worms. Our results indicate that dnc-1 KD in C. elegans is a useful model for the screening of drugs against motor neuron degeneration, and that MWT is a powerful tool for the behavior-based screening of drugs.

摘要

肌萎缩侧索硬化症(ALS)是一种致命的神经退行性疾病,其特征是运动神经元逐渐丧失,目前尚无有效的治疗方法。此前,我们构建了一个肌萎缩侧索硬化症的秀丽隐杆线虫模型,该模型中特异性地在运动神经元中敲低了 dnc-1(人动力蛋白激活蛋白 1 同源物)的表达。该 dnc-1 KD 模型表现出进行性运动缺陷以及轴突和神经元变性,这与 ALS 患者的情况相似。在本研究中,我们使用该 dnc-1 KD 模型和 Multi-Worm Tracker(MWT)建立了一种基于行为的、自动化的、定量的药物筛选系统,并测试了 38 种候选神经保护化合物是否能改善 dnc-1 KD 动物的运动能力。我们发现,包括利鲁唑(一种已批准用于 ALS 患者的药物)在内的 12 种化合物能改善 dnc-1 KD 动物的表型。钙通道阻滞剂硝苯地平能最有效地改善 dnc-1 KD 动物的运动障碍和轴突变性。硝苯地平还能改善其他运动神经元变性线虫模型,包括 dnc-1 突变体和过表达人 TAR DNA 结合蛋白 43kDa 的线虫的运动缺陷。我们的研究结果表明,秀丽隐杆线虫中的 dnc-1 KD 是筛选针对运动神经元变性药物的有用模型,MWT 是一种基于行为的药物筛选的强大工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19cb/6626054/f57851b996bb/41598_2019_46642_Fig1_HTML.jpg

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