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小胶质细胞形态计量分析:选择众多,一致性却很差。

Microglial morphometric analysis: so many options, so little consistency.

作者信息

Reddaway Jack, Richardson Peter Eulalio, Bevan Ryan J, Stoneman Jessica, Palombo Marco

机构信息

Division of Neuroscience, School of Biosciences, Cardiff University, Cardiff, United Kingdom.

Hodge Centre for Neuropsychiatric Immunology, Neuroscience and Mental Health Innovation Institute (NMHII), Cardiff University, Cardiff, United Kingdom.

出版信息

Front Neuroinform. 2023 Aug 10;17:1211188. doi: 10.3389/fninf.2023.1211188. eCollection 2023.

Abstract

Quantification of microglial activation through morphometric analysis has long been a staple of the neuroimmunologist's toolkit. Microglial morphological phenomics can be conducted through either manual classification or constructing a digital skeleton and extracting morphometric data from it. Multiple open-access and paid software packages are available to generate these skeletons via semi-automated and/or fully automated methods with varying degrees of accuracy. Despite advancements in methods to generate morphometrics (quantitative measures of cellular morphology), there has been limited development of tools to analyze the datasets they generate, in particular those containing parameters from tens of thousands of cells analyzed by fully automated pipelines. In this review, we compare and critique the approaches using cluster analysis and machine learning driven predictive algorithms that have been developed to tackle these large datasets, and propose improvements for these methods. In particular, we highlight the need for a commitment to from groups developing these classifiers. Furthermore, we call attention to a need for communication between those with a strong software engineering/computer science background and neuroimmunologists to produce effective analytical tools with simplified operability if we are to see their wide-spread adoption by the glia biology community.

摘要

长期以来,通过形态计量分析对小胶质细胞激活进行定量一直是神经免疫学家工具包的一项主要内容。小胶质细胞形态表型学可以通过人工分类或构建数字骨架并从中提取形态计量数据来进行。有多个开放获取和付费软件包可通过半自动和/或全自动方法生成这些骨架,其准确性各不相同。尽管在生成形态计量学(细胞形态的定量测量)的方法方面取得了进展,但用于分析它们所生成数据集的工具开发有限,特别是那些包含通过全自动管道分析的数万个细胞参数的数据集。在这篇综述中,我们比较并批评了使用聚类分析和机器学习驱动的预测算法来处理这些大型数据集的方法,并对这些方法提出了改进建议。特别是,我们强调开发这些分类器的团队需要做出承诺。此外,我们提请注意,如果要让神经胶质生物学界广泛采用这些有效分析工具,那么具有强大软件工程/计算机科学背景的人员与神经免疫学家之间需要进行沟通,以生产出具有简化操作性的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08f5/10448193/ac006585de1d/fninf-17-1211188-g001.jpg

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