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Investigating dynamic structural and mechanical changes of neuroblastoma cells associated with glutamate-mediated neurodegeneration

机译:研究与谷氨酸介导的神经变性相关的神经母细胞瘤细胞的动态结构和机械变化

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摘要

Glutamate-mediated neurodegeneration resulting from excessive activation of glutamate receptors is recognized as one of the major causes of various neurological disorders such as Alzheimer's and Huntington's diseases. However, the underlying mechanisms in the neurodegenerative process remain unidentified. Here, we investigate the real-time dynamic structural and mechanical changes associated with the neurodegeneration induced by the activation of N-methyl-D-aspartate (NMDA) receptors (a subtype of glutamate receptors) at the nanoscale. Atomic force microscopy (AFM) is employed to measure the three-dimensional (3-D) topography and mechanical properties of live SH-SY5Y cells under stimulus of NMDA receptors. A significant increase in surface roughness and stiffness of the cell is observed after NMDA treatment, which indicates the time-dependent neuronal cell behavior under NMDA-mediated neurodegeneration. The present AFM based study further advance our understanding of the neurodegenerative process to elucidate the pathways and mechanisms that govern NMDA induced neurodegeneration, so as to facilitate the development of novel therapeutic strategies for neurodegenerative diseases.
机译:由谷氨酸受体的过度活化引起的谷氨酸介导的神经变性被认为是各种神经系统疾病如阿尔茨海默氏病和亨廷顿氏病的主要原因之一。但是,神经退行性过程中的潜在机制仍不清楚。在这里,我们研究了与纳米级N-甲基-D-天冬氨酸(NMDA)受体(谷氨酸受体的一种亚型)的激活所诱导的神经变性相关的实时动态结构和机械变化。原子力显微镜(AFM)用于在NMDA受体刺激下测量活SH-SY5Y细胞的三维(3-D)形貌和力学性能。 NMDA处理后,观察到细胞表面粗糙度和刚度显着增加,这表明在NMDA介导的神经变性下,时间依赖性神经元细胞行为。目前基于AFM的研究进一步提高了我们对神经退行性过程的理解,以阐明控制NMDA诱导的神经退行性的途径和机制,从而促进了神经退行性疾病的新型治疗策略的发展。

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