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Modulation of α-synuclein expression in transgenic animals for modelling synucleinopathies — is the juice worth the squeeze?

机译:调节转基因动物中α-突触核蛋白表达以模拟突触核蛋白病-这种汁液值得吗?

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摘要

Studies of various animal models have made a substantial contribution to the recent progress in understanding the molecular and cellular basis of neurodegenerative disorders. Modelling of neuro-degeneration by genetic alteration of laboratory animals became one of the most powerful tools of modern experimental neurology. The crucial event in pathogenesis of neurodegenerative diseases known as synucleinopathies is modification of α-synuclein metabolism caused by missense mutations, increased expression of the gene, or impaired degradation or intracellular compart-mentalisation of the protein. Therefore, manipulations with expression of α-synuclein in laboratory animals were widely used for creating models of these diseases. In the present review we discuss strong and weak sides of such models, what has been already learned from studies of these animals and what types of models might be useful to further our knowledge about pathogenesis of different synucleinopathies.
机译:各种动物模型的研究对了解神经退行性疾病的分子和细胞基础的最新进展做出了重大贡献。通过实验动物遗传改变对神经变性进行建模成为现代实验神经学最强大的工具之一。在神经退行性疾病的发病机理中被称为突触核蛋白病的关键事件是由错义突变,基因表达增加,蛋白质的降解或细胞内分隔受损引起的α-突触核蛋白代谢修饰。因此,在实验动物中对α-突触核蛋白表达的操纵被广泛用于创建这些疾病的模型。在本综述中,我们将讨论此类模型的优缺点,从对这些动物的研究中了解到的内容以及哪些类型的模型可能有助于进一步了解不同突触核蛋白病的发病机理。

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