Department of Neuroscience, Brown University, 185 Meeting Street, Providence, RI 02912, USA.
Neurobiol Dis. 2010 Oct;40(1):4-11. doi: 10.1016/j.nbd.2010.05.012. Epub 2010 May 19.
Neurodegenerative diseases impose a burden on society, yet for the most part, the mechanisms underlying neuronal dysfunction and death in these disorders remain unclear despite the identification of relevant disease genes. Given the molecular conservation in neuronal signaling pathways across vertebrate and invertebrate species, many researchers have turned to the nematode Caenorhabditis elegans to identify the mechanisms underlying neurodegenerative disease pathology. C. elegans can be engineered to express human proteins associated with neurodegeneration; additionally, the function of C. elegans orthologs of human neurodegenerative disease genes can be dissected. Herein, we examine major C. elegans neurodegeneration models that recapitulate many aspects of human neurodegenerative disease and we survey the screens that have identified modifier genes. This review highlights how the C. elegans community has used this versatile organism to model several aspects of human neurodegeneration and how these studies have contributed to our understanding of human disease.
神经退行性疾病给社会带来了沉重负担,但尽管已经确定了相关的疾病基因,这些疾病中神经元功能障碍和死亡的机制在很大程度上仍不清楚。鉴于神经元信号通路在脊椎动物和无脊椎动物物种中的分子保守性,许多研究人员转向秀丽隐杆线虫来确定神经退行性疾病病理学的机制。可以设计线虫来表达与人神经退行性疾病相关的人类蛋白;此外,还可以剖析秀丽隐杆线虫与人神经退行性疾病基因的同源物的功能。本文中,我们研究了再现人类神经退行性疾病许多方面的主要秀丽隐杆线虫神经退行性变模型,并调查了已鉴定修饰基因的筛选。这篇综述强调了秀丽隐杆线虫社区如何利用这种多功能生物来模拟人类神经退行性变的几个方面,以及这些研究如何促进我们对人类疾病的理解。