Heindl Steffanie, Gesierich Benno, Benakis Corinne, Llovera Gemma, Duering Marco, Liesz Arthur
Institute for Stroke and Dementia Research, University Hospital, Ludwig-Maximilians-Universität München, Munich, Germany.
Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
Front Cell Neurosci. 2018 Apr 19;12:106. doi: 10.3389/fncel.2018.00106. eCollection 2018.
Microglia are the resident immune cells of the brain and react quickly to changes in their environment with transcriptional regulation and morphological changes. Brain tissue injury such as ischemic stroke induces a local inflammatory response encompassing microglial activation. The change in activation status of a microglia is reflected in its gradual morphological transformation from a highly ramified into a less ramified or amoeboid cell shape. For this reason, the morphological changes of microglia are widely utilized to quantify microglial activation and studying their involvement in virtually all brain diseases. However, the currently available methods, which are mainly based on manual rating of immunofluorescent microscopic images, are often inaccurate, rater biased, and highly time consuming. To address these issues, we created a fully automated image analysis tool, which enables the analysis of microglia morphology from a confocal Z-stack and providing up to 59 morphological features. We developed the algorithm on an exploratory dataset of microglial cells from a stroke mouse model and validated the findings on an independent data set. In both datasets, we could demonstrate the ability of the algorithm to sensitively discriminate between the microglia morphology in the peri-infarct and the contralateral, unaffected cortex. Dimensionality reduction by principal component analysis allowed to generate a highly sensitive compound score for microglial shape analysis. Finally, we tested for concordance of results between the novel automated analysis tool and the conventional manual analysis and found a high degree of correlation. In conclusion, our novel method for the fully automatized analysis of microglia morphology shows excellent accuracy and time efficacy compared to traditional analysis methods. This tool, which we make openly available, could find application to study microglia morphology using fluorescence imaging in a wide range of brain disease models.
小胶质细胞是大脑中的常驻免疫细胞,会通过转录调控和形态变化对其周围环境的变化迅速做出反应。诸如缺血性中风之类的脑组织损伤会引发包括小胶质细胞激活在内的局部炎症反应。小胶质细胞激活状态的变化反映在其形态从高度分支逐渐转变为分支较少或类阿米巴样细胞形状。因此,小胶质细胞的形态变化被广泛用于量化小胶质细胞的激活情况,并研究它们在几乎所有脑部疾病中的作用。然而,目前可用的方法主要基于对免疫荧光显微镜图像的人工评分,往往不准确、存在评分者偏差且耗时极长。为了解决这些问题,我们创建了一个全自动图像分析工具,该工具能够从共聚焦Z轴堆栈分析小胶质细胞形态,并提供多达59种形态特征。我们在一个中风小鼠模型的小胶质细胞探索性数据集中开发了该算法,并在一个独立数据集上验证了研究结果。在这两个数据集中,我们都能够证明该算法能够灵敏地区分梗死灶周围和对侧未受影响皮质中的小胶质细胞形态。通过主成分分析进行降维,能够生成用于小胶质细胞形状分析的高灵敏度复合评分。最后,我们测试了新型自动化分析工具与传统人工分析结果之间的一致性,发现两者具有高度相关性。总之,与传统分析方法相比,我们用于小胶质细胞形态全自动分析的新方法具有出色的准确性和时效性。我们公开提供的这个工具可用于在广泛的脑部疾病模型中使用荧光成像研究小胶质细胞形态。