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使用扫描离子电导显微镜实时测定神经母细胞瘤细胞中聚集的α-突触核蛋白诱导的膜破裂。

Real-time determination of aggregated alpha-synuclein induced membrane disruption at neuroblastoma cells using scanning ion conductance microscopy.

机构信息

Department of Chemistry and Biochemistry, California State University Los Angeles, 5151 State University Dr., Los Angeles, CA 90032, USA.

出版信息

Faraday Discuss. 2018 Oct 1;210(0):131-143. doi: 10.1039/c8fd00059j.

Abstract

Parkinson's disease (PD) is recognized as the second most common neurodegenerative disorder and has affected approximately one million people in the United States alone. A large body of evidence has suggested that deposition of aggregated alpha-synuclein (α-Syn), a brain protein abundant near presynaptic termini, in intracellular protein inclusions (Lewy bodies) results in neuronal cell damage and ultimately contributes to the progression of PD. However, the exact mechanism is still unclear. One hypothesis is that α-Syn aggregates disrupt the cell membrane's integrity, eventually leading to cell death. We used scanning ion conductance microscopy (SICM) to monitor the morphological changes of SH-SY5Y neuroblastoma cells and observed dramatic disruption of the cell membrane after adding α-Syn aggregates to the culturing media. This work demonstrates that SICM can be applied as a new approach to studying the cytotoxicity of α-Syn aggregates.

摘要

帕金森病(PD)被认为是第二常见的神经退行性疾病,仅在美国就影响了大约 100 万人。大量证据表明,聚集的α-突触核蛋白(α-Syn)的沉积,这种在突触前末端附近丰富的脑蛋白,在细胞内蛋白质包涵体(路易体)中,导致神经元细胞损伤,并最终导致 PD 的进展。然而,确切的机制尚不清楚。一种假设是,α-Syn 聚集体破坏了细胞膜的完整性,最终导致细胞死亡。我们使用扫描离子电导显微镜(SICM)来监测 SH-SY5Y 神经母细胞瘤细胞的形态变化,并观察到在向培养介质中添加 α-Syn 聚集体后,细胞膜出现明显的破坏。这项工作表明,SICM 可以作为一种新的方法来研究 α-Syn 聚集体的细胞毒性。

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