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α-突触核蛋白纤维化与帕金森病之间是否存在因果关系?

Is there a cause-and-effect relationship between alpha-synuclein fibrillization and Parkinson's disease?

作者信息

Goldberg M S, Lansbury P T

机构信息

Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Department of Neurology, Boston, MA 02115, USA.

出版信息

Nat Cell Biol. 2000 Jul;2(7):E115-9. doi: 10.1038/35017124.

Abstract

The first gene to be linked to Parkinson's disease encodes the neuronal protein alpha-synuclein. Recent mouse and Drosophila models of Parkinson's disease support a central role for the process of alpha-synuclein fibrillization in pathogenesis. However, some evidence indicates that the fibril itself may not be the pathogenic species. Our own biophysical studies suggest that a structured fibrillization intermediate or an alternatively assembled oligomer may be responsible for neuronal death. This speculation can now be experimentally tested in the animal models. Such experiments will have implications for the development of new therapies for Parkinson's disease and related neurodegenerative diseases.

摘要

首个与帕金森病相关联的基因编码神经元蛋白α-突触核蛋白。最近的帕金森病小鼠和果蝇模型支持α-突触核蛋白纤维化过程在发病机制中起核心作用。然而,一些证据表明,纤维本身可能不是致病物质。我们自己的生物物理研究表明,一种结构化的纤维化中间体或另一种组装的寡聚体可能是神经元死亡的原因。这种推测现在可以在动物模型中进行实验验证。此类实验将对帕金森病及相关神经退行性疾病新疗法的开发产生影响。

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