利用R6转基因亨廷顿氏病小鼠模型试图开发新的治疗策略

Jia Yi Li, Natalija Popovic, Patrik Brundin
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引用次数: 171

摘要

亨廷顿氏病(HD)是一种遗传性神经退行性疾病。自1993年发现致病基因以来,已经产生了许多HD的转基因动物模型。第一批转基因小鼠模型R6/1和R6/2系是在8年前建立的。R6/2小鼠是研究HD发病机制和治疗干预措施最具特征和应用最广泛的模型。在目前的回顾中,我们特别关注R6转基因小鼠模型的特点,并更详细地描述了在这些小鼠中测试的不同治疗策略。最后,我们还批判性地评估了HD小鼠模型与人类疾病的相关性,并讨论了如何在未来最好地使用它们。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Use of the R6 Transgenic Mouse Models of Huntington's Disease in Attempts to Develop Novel Therapeutic Strategies

Huntington's disease (HD) is a genetic neurodegenerative disorder. Since identification of the disease-causing gene in 1993, a number of genetically modified animal models of HD have been generated. The first transgenic mouse models, R6/1 and R6/2 lines, were established 8 years ago. The R6/2 mice have been the best characterized and the most widely used model to study pathogenesis of HD and therapeutic interventions. In the present review, we especially focus on the characteristics of R6 transgenic mouse models and, in greater detail, describe the different therapeutic strategies that have been tested in these mice. We also, at the end, critically assess the relevance of the HD mouse models compared with the human disease and discuss how they can be best used in the future.

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