Novel high-content and open-source image analysis tools for profiling mitochondrial morphology in neurological cell models

IF 2.7 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Marcus Y. Chin , David A. Joy , Madhuja Samaddar, Anil Rana, Johann Chow, Takashi Miyamoto, Meredith Calvert
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引用次数: 0

Abstract

Mitochondria undergo dynamic morphological changes depending on cellular cues, stress, genetic factors, or disease. The structural complexity and disease-relevance of mitochondria have stimulated efforts to generate image analysis tools for describing mitochondrial morphology for therapeutic development. Using high-content analysis, we measured multiple morphological parameters and employed unbiased feature clustering to identify the most robust pair of texture metrics that described mitochondrial state. Here, we introduce a novel image analysis pipeline to enable rapid and accurate profiling of mitochondrial morphology in various cell types and pharmacological perturbations. We applied a high-content adapted implementation of our tool, MitoProfilerHC, to quantify mitochondrial morphology changes in i) a mammalian cell dose response study and ii) compartment-specific drug effects in primary neurons. Next, we expanded the usability of our pipeline by using napari, a Python-powered image analysis tool, to build an open-source version of MitoProfiler and validated its performance and applicability. In conclusion, we introduce MitoProfiler as both a high-content-based and an open-source method to accurately quantify mitochondrial morphology in cells, which we anticipate to greatly facilitate mechanistic discoveries in mitochondrial biology and disease.
用于分析神经细胞模型中线粒体形态的新型高含量和开源图像分析工具。
线粒体经历动态形态变化取决于细胞线索,压力,遗传因素,或疾病。线粒体的结构复杂性和疾病相关性促使人们努力生成图像分析工具,用于描述治疗开发的线粒体形态。通过高含量分析,我们测量了多个形态参数,并采用无偏特征聚类来识别描述线粒体状态的最稳健的纹理指标对。在这里,我们引入了一种新的图像分析管道,可以快速准确地分析各种细胞类型和药理扰动下的线粒体形态。我们应用了我们的工具MitoProfilerHC的高含量适应性实现,量化了i)哺乳动物细胞剂量反应研究和ii)初级神经元中室特异性药物效应的线粒体形态学变化。接下来,我们通过使用napari(一个python驱动的图像分析工具)来扩展管道的可用性,构建开源版本的MitoProfiler,并验证其性能和适用性。总之,我们介绍MitoProfiler作为一种基于高含量和开源的方法来准确量化细胞中的线粒体形态,我们预计这将极大地促进线粒体生物学和疾病的机制发现。
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来源期刊
SLAS Discovery
SLAS Discovery Chemistry-Analytical Chemistry
CiteScore
7.00
自引率
3.20%
发文量
58
审稿时长
39 days
期刊介绍: Advancing Life Sciences R&D: SLAS Discovery reports how scientists develop and utilize novel technologies and/or approaches to provide and characterize chemical and biological tools to understand and treat human disease. SLAS Discovery is a peer-reviewed journal that publishes scientific reports that enable and improve target validation, evaluate current drug discovery technologies, provide novel research tools, and incorporate research approaches that enhance depth of knowledge and drug discovery success. SLAS Discovery emphasizes scientific and technical advances in target identification/validation (including chemical probes, RNA silencing, gene editing technologies); biomarker discovery; assay development; virtual, medium- or high-throughput screening (biochemical and biological, biophysical, phenotypic, toxicological, ADME); lead generation/optimization; chemical biology; and informatics (data analysis, image analysis, statistics, bio- and chemo-informatics). Review articles on target biology, new paradigms in drug discovery and advances in drug discovery technologies. SLAS Discovery is of particular interest to those involved in analytical chemistry, applied microbiology, automation, biochemistry, bioengineering, biomedical optics, biotechnology, bioinformatics, cell biology, DNA science and technology, genetics, information technology, medicinal chemistry, molecular biology, natural products chemistry, organic chemistry, pharmacology, spectroscopy, and toxicology. SLAS Discovery is a member of the Committee on Publication Ethics (COPE) and was published previously (1996-2016) as the Journal of Biomolecular Screening (JBS).
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