基于干细胞的检测平台证明了患者皮质神经元的突触功能障碍取决于α-突触核蛋白。

IF 6.7 1区 医学 Q1 NEUROSCIENCES
Andrew J White, Karis A Clark, Kellianne D Alexander, Nagendran Ramalingam, Tracy L Young-Pearse, Ulf Dettmer, Dennis J Selkoe, Gary P H Ho
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引用次数: 0

摘要

大脑皮层中富含α-突触核蛋白(αS)的路易体和神经元与帕金森病(PD)和路易体痴呆症(DLB)中痴呆症的存在有关,但αS是否会影响人类大脑皮层神经元中突触小泡的动力学尚不清楚。我们利用一种新的基于 iPSC 的检测平台来测量突触囊泡循环,结果发现,在人类大脑皮层谷氨酸能神经元中,转基因表达或患者来源神经元中内源性基因座的三倍复制导致的 αS 增加会减少刺激和自发条件下的突触囊泡循环。因此,我们利用一个稳健、易于采用的检测平台,首次展示了αS诱导的人类皮质神经元突触功能障碍,而突触功能障碍是帕金森病痴呆症和DLB的关键细胞基质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A stem cell-based assay platform demonstrates alpha-synuclein dependent synaptic dysfunction in patient-derived cortical neurons.

A stem cell-based assay platform demonstrates alpha-synuclein dependent synaptic dysfunction in patient-derived cortical neurons.

Alpha-synuclein (αS)-rich Lewy bodies and neurites in the cerebral cortex correlate with the presence of dementia in Parkinson disease (PD) and Dementia with Lewy bodies (DLB), but whether αS influences synaptic vesicle dynamics in human cortical neurons is unknown. Using a new iPSC-based assay platform for measuring synaptic vesicle cycling, we found that in human cortical glutamatergic neurons, increased αS from either transgenic expression or triplication of the endogenous locus in patient-derived neurons reduced synaptic vesicle cycling under both stimulated and spontaneous conditions. Thus, using a robust, easily adopted assay platform, we show for the first time αS-induced synaptic dysfunction in human cortical neurons, a key cellular substrate for PD dementia and DLB.

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来源期刊
NPJ Parkinson's Disease
NPJ Parkinson's Disease Medicine-Neurology (clinical)
CiteScore
9.80
自引率
5.70%
发文量
156
审稿时长
11 weeks
期刊介绍: npj Parkinson's Disease is a comprehensive open access journal that covers a wide range of research areas related to Parkinson's disease. It publishes original studies in basic science, translational research, and clinical investigations. The journal is dedicated to advancing our understanding of Parkinson's disease by exploring various aspects such as anatomy, etiology, genetics, cellular and molecular physiology, neurophysiology, epidemiology, and therapeutic development. By providing free and immediate access to the scientific and Parkinson's disease community, npj Parkinson's Disease promotes collaboration and knowledge sharing among researchers and healthcare professionals.
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