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神经退行性疾病中的突触核蛋白病:共犯、内部作案与选择性易损性。

Synucleinopathies in neurodegenerative diseases: Accomplices, an inside job and selective vulnerability.

作者信息

Azizi S Ausim, Azizi Saara-Anne

机构信息

Department of Neurology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 10140, United States.

Pritzker School of Medicine, University of Chicago, Chicago, Il 60637, United States.

出版信息

Neurosci Lett. 2018 Apr 13;672:150-152. doi: 10.1016/j.neulet.2017.12.003. Epub 2017 Dec 5.

Abstract

Pathogenesis of degenerative diseases is complex and multifaceted. The disease phenotypes depend on the location of injury/damage in the brain networks and pathologically are characterized by loss of brain cells. The reason for this loss appears to be an accumulation of misfolded and dysfunctional proteins that trigger apoptotic cell death. The role of alpha-synuclein mutations, its interaction with other proteins and the cellular environment is discussed in the context of selective neuron loss.

摘要

退行性疾病的发病机制复杂且多方面。疾病表型取决于脑网络中损伤/损害的位置,病理上以脑细胞丢失为特征。这种丢失的原因似乎是错误折叠和功能失调的蛋白质积累,从而引发细胞凋亡性死亡。在选择性神经元丢失的背景下,讨论了α-突触核蛋白突变的作用、其与其他蛋白质以及细胞环境的相互作用。

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