Palikaras Konstantinos, Tavernarakis Nektarios
Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, Greece; Department of Basic Sciences, Faculty of Medicine, University of Crete, Heraklion, 70013, Crete, Greece;
J Vis Exp. 2020 Aug 15(162). doi: 10.3791/61169.
Battling human neurodegenerative pathologies and managing their pervasive socioeconomic impact is becoming a global priority. Notwithstanding their detrimental effects on the human life quality and the healthcare system, the majority of human neurodegenerative disorders still remain incurable and non-preventable. Therefore, the development of novel therapeutic interventions against such maladies is becoming a pressing urgency. Age-associated deterioration of neuronal circuits and function is evolutionarily conserved in organisms as diverse as the lowly worm Caenorhabditis elegans and humans, signifying similarities in the underlying cellular and molecular mechanisms. C. elegans is a highly malleable genetic model, which offers a well-characterized nervous system, body transparency and a diverse repertoire of genetic and imaging techniques to assess neuronal activity and quality control during ageing. Here, we introduce and describe methodologies utilizing some versatile nematode models, including hyperactivated ion channel-induced necrosis (e.g., deg-3(d) and mec-4(d)) and protein aggregate (e.g., α-syunclein and poly-glutamate)-induced neurotoxicity, to monitor and dissect the cellular and molecular underpinnings of age-related neuronal breakdown. A combination of these animal neurodegeneration models, together with genetic and pharmacological screens for cell death modulators will lead to an unprecedented understanding of age-related breakdown of neuronal function and will provide critical insights with broad relevance to human health and quality of life.
对抗人类神经退行性疾病并应对其广泛的社会经济影响正成为全球的优先事项。尽管这些疾病对人类生活质量和医疗系统有不利影响,但大多数人类神经退行性疾病仍然无法治愈且无法预防。因此,开发针对此类疾病的新型治疗干预措施变得迫在眉睫。神经元回路和功能的年龄相关性衰退在从低等线虫秀丽隐杆线虫到人类等多种生物中都具有进化保守性,这表明其潜在的细胞和分子机制具有相似性。秀丽隐杆线虫是一种具有高度可塑性的遗传模型,它提供了一个特征明确的神经系统、身体透明度以及多种遗传和成像技术,用于评估衰老过程中的神经元活动和质量控制。在这里,我们介绍并描述利用一些通用线虫模型的方法,包括超激活离子通道诱导的坏死(例如,deg-3(d)和mec-4(d))以及蛋白质聚集体(例如,α-突触核蛋白和多聚谷氨酸)诱导的神经毒性,以监测和剖析与年龄相关的神经元衰退的细胞和分子基础。这些动物神经退行性模型与细胞死亡调节剂的遗传和药理学筛选相结合,将使我们对与年龄相关的神经元功能衰退有前所未有的理解,并将为与人类健康和生活质量广泛相关的关键见解提供依据。