MRC Centre for Developmental and Biomedical Genetics, Department of Biomedical Sciences, University of Sheffield, Sheffield, UK.
Adv Genet. 2011;73:1-50. doi: 10.1016/B978-0-12-380860-8.00001-X.
Parkinson's disease (PD) is the second most prevalent neurodegenerative disorder principally affecting the dopaminergic neurons of the substantia nigra. The pathogenic mechanisms are unknown and there are currently no cure or disease-modifying therapies. Recent genetic linkage studies have begun to identify single-gene mutations responsible for rare heritable forms of PD and define genetic risk factors contributing to disease prevalence in sporadic cases. These findings provide an opportunity to gain insight into the molecular mechanisms of this disorder through the creation and analysis of appropriate genetic models. One model system that has proven surprisingly tractable for these studies is the fruit fly, Drosophila melanogaster. Analysis of a number of Drosophila models of PD has revealed some profound and sometimes surprising insights into PD pathogenesis. Moreover, these models can be used to investigate potential therapeutic strategies that may be effective in vivo, and tests have highlighted the efficacy of a number of neuroprotective compounds. Here, I review the methodologies employed in developing the various Drosophila models, and the recent advances that these models in particular have contributed to our understanding of the mechanisms that underlie PD pathogenesis and possible treatment strategies.
帕金森病(PD)是第二大常见的神经退行性疾病,主要影响黑质中的多巴胺能神经元。其发病机制尚不清楚,目前尚无治愈或疾病修饰疗法。最近的遗传连锁研究已开始确定导致罕见遗传性 PD 形式的单基因突变,并确定导致散发性病例疾病流行的遗传风险因素。这些发现为通过创建和分析适当的遗传模型,深入了解该疾病的分子机制提供了机会。在这些研究中,一种已被证明非常可行的模型系统是果蝇,黑腹果蝇。对许多 PD 果蝇模型的分析揭示了一些关于 PD 发病机制的深刻而有时令人惊讶的见解。此外,这些模型可用于研究可能在体内有效的潜在治疗策略,并且测试突出了许多神经保护化合物的功效。在这里,我回顾了开发各种果蝇模型所采用的方法,以及这些模型特别是在我们对 PD 发病机制和可能的治疗策略的理解方面所做出的最新进展。