Rees Daniel J, Roberts Luke, Carla Carisi M, Morgan Alwena H, Brown M Rowan, Davies Jeffrey S
Molecular Neurobiology, Institute of Life Sciences, School of Medicine, Swansea University, Swansea, United Kingdom.
Centre for Nanohealth, College of Engineering, Swansea University, Swansea, United Kingdom.
Curr Protoc Neurosci. 2020 Dec;94(1):e105. doi: 10.1002/cpns.105.
Neuronal mitochondrial fragmentation is a phenotype exhibited in models of neurodegeneration such as Parkinson's disease. Delineating the dysfunction in mitochondrial dynamics found in diseased states can aid our understanding of underlying mechanisms of disease progression and possibly identify novel therapeutic approaches. Advances in microscopy and the availability of intuitive open-access software have accelerated the rate of image acquisition and analysis, respectively. These developments allow routine biology researchers to rapidly turn hypotheses into results. In this protocol, we describe the utilization of cell culture techniques, high-content imaging (HCI), and the subsequent open-source image analysis pipeline for the quantification of mitochondrial fragmentation in the context of a rotenone-based in vitro Parkinson's disease model. © 2020 The Authors. Basic Protocol 1: SN4741 neuron culture and treatment in a rotenone-based model of Parkinson's disease Basic Protocol 2: Identification of cell nuclei, measurement of mitochondrial membrane potential, and measurement of mitochondrial fragmentation in mouse-derived midbrain dopaminergic neurons.
神经元线粒体碎片化是在帕金森病等神经退行性疾病模型中表现出的一种表型。描绘疾病状态下线粒体动力学的功能障碍有助于我们理解疾病进展的潜在机制,并有可能确定新的治疗方法。显微镜技术的进步和直观的开源软件的可用性分别加快了图像采集和分析的速度。这些进展使常规生物学研究人员能够迅速将假设转化为结果。在本方案中,我们描述了在基于鱼藤酮的体外帕金森病模型中,利用细胞培养技术、高内涵成像(HCI)以及随后的开源图像分析流程来量化线粒体碎片化。© 2020作者。基本方案1:在基于鱼藤酮的帕金森病模型中培养和处理SN4741神经元 基本方案2:鉴定细胞核、测量线粒体膜电位以及测量小鼠中脑多巴胺能神经元中的线粒体碎片化。