2015
DOI: 10.1007/s12021-015-9267-4
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Automatic Dendritic Length Quantification for High Throughput Screening of Mature Neurons

Abstract: High-throughput automated fluorescent imaging and screening are important for studying neuronal development, functions, and pathogenesis. An automatic approach of analyzing images acquired in automated fashion, and quantifying dendritic characteristics is critical for making such screens high-throughput. However, automatic and effective algorithms and tools, especially for the images of mature mammalian neurons with complex arbors, have been lacking. Here, we present algorithms and a tool for quantifying dendr… Show more

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Cited by 9 publications
(7 citation statements)
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“…These and other measures enabled us to detect fluorescence signals specifically in cell bodies and neuronal processes in our human Ngn2-differentiated cultures, which represents, to our knowledge, unprecedented levels of neuronal density for cultures used in high-content screening, in comparison to previous work on automated segmentation approaches for rodent-derived neuronal cultures (e.g. 52,53 ). Additionally, with the goal of rapidly screening large collections of small molecules, our aim was to achieve image acquisition and segmentation in a single, microwell oriented platform, which was afforded by the IN Cell Analyzer 6000 imaging system.…”
Section: Discussionmentioning
confidence: 92%
“…These and other measures enabled us to detect fluorescence signals specifically in cell bodies and neuronal processes in our human Ngn2-differentiated cultures, which represents, to our knowledge, unprecedented levels of neuronal density for cultures used in high-content screening, in comparison to previous work on automated segmentation approaches for rodent-derived neuronal cultures (e.g. 52,53 ). Additionally, with the goal of rapidly screening large collections of small molecules, our aim was to achieve image acquisition and segmentation in a single, microwell oriented platform, which was afforded by the IN Cell Analyzer 6000 imaging system.…”
Section: Discussionmentioning
confidence: 92%
“…For example, analysis of changes in cell morphology, such as dendritic beading and cellular blebbing, could quantify early stages of necrosis and changes in nuclear structure are commonly extracted in high content analysis approaches to detect apoptosis (Anilkumar et al, 2017). Because the ImageJ and CellProfiler platforms are widely used for high content image analysis (Vokes and Carpenter, 2008; Smafield et al, 2015), the workflows described here may easily be expanded to analyze additional features.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, image time series should be analysed by suitable computational software enabling automated or semi-automated image analysis. Though there are several computational tools for the analysis of filamentous growth of fungi 23 26 and neurites 30 37 available, to our best knowledge none of the available tools is intended for the analysis of the early hyphal development of multiple germlings at the same time. In general, many available analytical tools are designed for qualitative analysis of filamentous growth rather than quantitative analysis of multiple germling-events in parallel 23 25 .…”
Section: Discussionmentioning
confidence: 99%
“…Beside the tools that are developed and optimized for the analysis of fungal growth, we also considered tools designed for the analysis of filamentous growth of other cell types like bacteria 27 , plants 28 , and neurons 29 . Especially, for tracking and analysis of neural growth and branching, many different toolboxes/algorithms have been developed recently, and most of them are available as open source software 30 37 . Nevertheless, also these tools are either optimized for the analysis of a single neuron with focus in branching events or they are designed to distinguish cellular features (eg.…”
Section: Introductionmentioning
confidence: 99%