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辅因子(一种光和应激门控的光遗传学工具)在原代海马神经元培养物中的转染与激活

Transfection and Activation of CofActor, a Light and Stress Gated Optogenetic Tool, in Primary Hippocampal Neuron Cultures.

作者信息

Bunner Wyatt P, Dodson Rachel, Hughes Robert M, Szatmari Erzsebet M

机构信息

Department of Physical Therapy, East Carolina University, Greenville NC, United States.

Department of Chemistry, East Carolina University, Greenville NC, United States.

出版信息

Bio Protoc. 2021 Apr 20;11(8):e3990. doi: 10.21769/BioProtoc.3990.

Abstract

Proteins involved in neurodegeneration can be coupled with optogenetic reagents to create rapid and sensitive reporters to provide insight into the biochemical processes that mediate the progression of neurodegenerative disorders, including Alzheimer's Disease (AD). We have recently developed a novel optically-responsive tool (the ' system) that couples and (key players in early stage cytoskeletal abnormalities associated with neurodegenerative disorders) with to provide spatial and temporal resolution of oxidative and energetic stress-dependent biochemical events. In contrast to currently available small-molecule based biosensors for monitoring changes in the redox environment of the cell, CofActor is a , genetically encoded redox sensor that can be activated with precise and . Here we describe a protocol for the expression and activation of the CofActor system in dissociated hippocampal neuron cultures prepared from newborn mice. Cultures were transfected with Lipofectamine on the fifth day (DIV5), then exposed to cellular stress inducing stimuli, leading to the formation of actin-cofilin rods that can be observed using live cell imaging techniques. The protocol described here allows for studies of stress-related cytoskeletal dysregulation in live neurons exposed to neurodegenerative stimuli, such as toxic Aβ42 oligomers. Moreover, expression of the sensor in neurons isolated from transgenic mouse models of AD and/or mice KO for proteins involved in AD can advance our understanding of the molecular basis of early cytoskeletal dysfunctions associated with neurodegeneration.

摘要

参与神经退行性变的蛋白质可与光遗传学试剂结合,创建快速灵敏的报告分子,以深入了解介导神经退行性疾病(包括阿尔茨海默病(AD))进展的生化过程。我们最近开发了一种新型光响应工具(“系统”),该工具将与(神经退行性疾病相关早期细胞骨架异常的关键参与者)与相结合,以提供氧化和能量应激依赖性生化事件的空间和时间分辨率。与目前用于监测细胞氧化还原环境变化的基于小分子的生物传感器不同,CofActor是一种可通过精确的和激活的基因编码氧化还原传感器。在这里,我们描述了一种在新生小鼠制备的原代海马神经元培养物中表达和激活CofActor系统的方案。在第5天(DIV5)用脂质体转染培养物,然后暴露于诱导细胞应激的刺激物,导致形成肌动蛋白-丝切蛋白杆,可使用活细胞成像技术观察到。这里描述的方案允许研究暴露于神经退行性刺激(如有毒Aβ42寡聚体)的活神经元中与应激相关的细胞骨架失调。此外,在从AD转基因小鼠模型和/或AD相关蛋白敲除小鼠分离的神经元中表达该传感器,可以推进我们对与神经退行性变相关的早期细胞骨架功能障碍分子基础的理解。

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