Glaucoma and Retinal Neurodegenerative Disease Research Group, Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, United Kingdom.
Neural Circuit Development and Regeneration Research Group, Department of Biology, University of Leuven, Naamsestraat 61 box 2464, 3000, Leuven, Belgium.
Sci Rep. 2017 May 8;7(1):1576. doi: 10.1038/s41598-017-01747-8.
Microglia play an important role in the pathology of CNS disorders, however, there remains significant uncertainty about the neuroprotective/degenerative role of these cells due to a lack of techniques to adequately assess their complex behaviour in response to injury. Advancing microscopy techniques, transgenic lines and well-characterized molecular markers, have made histological assessment of microglia populations more accessible. However, there is a distinct lack of tools to adequately extract information from these images to fully characterise microglia behaviour. This, combined with growing economic pressures and the ethical need to minimise the use of laboratory animals, led us to develop tools to maximise the amount of information obtained. This study describes a novel approach, combining image analysis with spatial statistical techniques. In addition to monitoring morphological parameters and global changes in microglia density, nearest neighbour distance, and regularity index, we used cluster analyses based on changes in soma size and roundness to yield novel insights into the behaviour of different microglia phenotypes in a murine optic nerve injury model. These methods should be considered a generic tool to quantitatively assess microglia activation, to profile phenotypic changes into microglia subpopulations, and to map spatial distributions in virtually every CNS region and disease state.
小胶质细胞在中枢神经系统疾病的病理中起着重要作用,然而,由于缺乏充分评估其对损伤反应的复杂行为的技术,这些细胞的神经保护/退行性作用仍然存在很大的不确定性。先进的显微镜技术、转基因系和特征明确的分子标记,使小胶质细胞群体的组织学评估变得更加容易。然而,目前缺乏足够的工具来从这些图像中提取信息,以充分描述小胶质细胞的行为。再加上不断增长的经济压力和尽量减少使用实验动物的伦理需要,促使我们开发了一些工具,以最大限度地获取信息。本研究描述了一种新的方法,将图像分析与空间统计技术相结合。除了监测小胶质细胞形态参数和密度的全局变化、最近邻距离和规则指数外,我们还使用基于体部大小和圆度变化的聚类分析,为不同的小胶质细胞表型在鼠视神经损伤模型中的行为提供了新的见解。这些方法应该被视为一种通用的工具,用于定量评估小胶质细胞的激活,将表型变化描绘成小胶质细胞亚群,并绘制虚拟的每个中枢神经系统区域和疾病状态的空间分布。