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解剖果蝇翅膀中线粒体的克隆成像。

Clonal Imaging of Mitochondria in the Dissected Fly Wing.

作者信息

Maddison Daniel C, Mattedi Francesca, Vagnoni Alessio, Smith Gaynor Ann

机构信息

UK Dementia Research Institute, School of Medicine, Cardiff University, Cardiff CF24 4HQ, United Kingdom.

Department of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RX, United Kingdom.

出版信息

Cold Spring Harb Protoc. 2023 Feb 1;2023(2):100-105. doi: 10.1101/pdb.prot108051.

Abstract

Mitochondria are essential for long-term neuronal function and survival. They are maintained in neurons, including long axonal stretches, through dynamic processes such as fission, fusion, biogenesis, and mitophagy. Here, we describe a protocol for the in-depth morphological analysis of individual mitochondria in axons in vivo. Most mitochondrial analysis of axons is currently performed in vitro with neurons in a developmental state. Therefore, an understanding of the axonal mitochondrial network during aging in fully differentiated neurons and the long-term consequence of gene knockout is often not developed. By using a clonal system paired with fluorescent genetically encoded markers in the wing, we can visualize individual neurons (out of the whole bundle), including their long axons and the mitochondria that they contain, using confocal imaging. The clonal system also allows visualization of neurons with genetic perturbations that would otherwise be lethal if present in the whole organism, allowing investigators to bypass lethality. This protocol can further be adapted to measure the physiological and biochemical state of the mitochondria. Mitochondrial morphology and health in axons are tightly linked to aging, axon injury, and neurodegeneration; therefore, this method can be used to investigate mitochondrial dysfunction associated with novel genes or those linked to neurodegenerative disease and axonopathy.

摘要

线粒体对于神经元的长期功能和存活至关重要。它们通过诸如裂变、融合、生物发生和线粒体自噬等动态过程,在包括长轴突延伸在内的神经元中得以维持。在此,我们描述了一种用于在体内对轴突中单个线粒体进行深度形态学分析的方案。目前,大多数对轴突线粒体的分析是在体外对处于发育状态的神经元进行的。因此,对于完全分化的神经元在衰老过程中的轴突线粒体网络以及基因敲除的长期后果,人们往往缺乏了解。通过使用与翅膀中荧光基因编码标记配对的克隆系统,我们可以利用共聚焦成像可视化单个神经元(从整个束中分离出来),包括它们的长轴突以及其中所含的线粒体。该克隆系统还能使带有基因扰动的神经元可视化,而这些扰动若存在于整个生物体中则会导致致死,从而使研究人员能够绕过致死性问题。此方案还可进一步用于测量线粒体的生理和生化状态。轴突中线粒体的形态和健康与衰老、轴突损伤及神经退行性变紧密相关;因此,该方法可用于研究与新基因或与神经退行性疾病及轴索性疾病相关的线粒体功能障碍。

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