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用于量化果蝇神经退行性变的大规模组织学方法

Mass Histology to Quantify Neurodegeneration in Drosophila.

作者信息

Sunderhaus Elizabeth R, Kretzschmar Doris

机构信息

Oregon Institute of Occupational Health Sciences, Oregon Health & Sciences University.

Oregon Institute of Occupational Health Sciences, Oregon Health & Sciences University;

出版信息

J Vis Exp. 2016 Dec 15(118):54809. doi: 10.3791/54809.

Abstract

Progressive neurodegenerative diseases like Alzheimer's disease (AD) or Parkinson's disease (PD) are an increasing threat to human health worldwide. Although mammalian models have provided important insights into the underlying mechanisms of pathogenicity, the complexity of mammalian systems together with their high costs are limiting their use. Therefore, the simple but well-established Drosophila model-system provides an alternative for investigating the molecular pathways that are affected in these diseases. Besides behavioral deficits, neurodegenerative diseases are characterized by histological phenotypes such as neuronal death and axonopathy. To quantify neuronal degeneration and to determine how it is affected by genetic and environmental factors, we use a histological approach that is based on measuring the vacuoles in adult fly brains. To minimize the effects of systematic error and to directly compare sections from control and experimental flies in one preparation, we use the 'collar' method for paraffin sections. Neurodegeneration is then assessed by measuring the size and/or number of vacuoles that have developed in the fly brain. This can either be done by focusing on a specific region of interest or by analyzing the entire brain by obtaining serial sections that span the complete head. Therefore, this method allows one to measure not only severe degeneration but also relatively mild phenotypes that are only detectable in a few sections, as occurs during normal aging.

摘要

像阿尔茨海默病(AD)或帕金森病(PD)这样的进行性神经退行性疾病,正日益威胁着全球人类健康。尽管哺乳动物模型为致病性的潜在机制提供了重要见解,但哺乳动物系统的复杂性及其高昂成本限制了它们的应用。因此,简单但成熟的果蝇模型系统为研究这些疾病中受影响的分子途径提供了一种替代方法。除了行为缺陷外,神经退行性疾病还具有组织学表型特征,如神经元死亡和轴突病变。为了量化神经元变性并确定其如何受遗传和环境因素影响,我们采用一种基于测量成年果蝇大脑中液泡的组织学方法。为了尽量减少系统误差的影响,并在一次制备中直接比较对照果蝇和实验果蝇的切片,我们对石蜡切片采用“套环”法。然后通过测量果蝇大脑中形成的液泡的大小和/或数量来评估神经变性。这既可以通过聚焦于特定的感兴趣区域来完成,也可以通过获取跨越整个头部的连续切片来分析整个大脑来实现。因此,这种方法不仅可以测量严重的变性,还可以测量相对较轻的表型,这些表型只有在少数切片中才能检测到,就像在正常衰老过程中那样。

相似文献

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Drosophila models of neurodegenerative disease.神经退行性疾病的果蝇模型。
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