Condon Nicholas D, Stow Jennifer L, Wall Adam A
Institute for Molecular Biosciences (IMB) Microscopy, The University of Queensland, Brisbane, Australia.
IMB Centre for Inflammation Disease Research, The University of Queensland, Brisbane, Australia.
Bio Protoc. 2020 Jan 20;10(2):e3494. doi: 10.21769/BioProtoc.3494.
Cell surface protrusions include F-actin rich, wave-like ruffles that are erected transiently in response to stimuli and during cell migration. Macrophages are innate immune cells that ruffle constitutively and more dramatically in cells activated by pathogens. Dorsal ruffles and their resulting macropinosomes are key sites for environmental sampling, pathogen detection and immune signaling. Quantitative assessment of ruffling is important for assessing pathogen responses in macrophages and for analysis of growth factor responses in other cell types but automated and quantitative methods are lacking, and rely on manual and qualitative assessments. Here we present an automated ImageJ macro for quantifying dorsal cell surface protrusions from 3D microscope images. The assay presented here is suitable for high-throughput screening applications to detect drug, pathogen, or growth factor induced changes in cell ruffling by measuring ruffle area and intensity and providing normalized values in an easy to read combined spreadsheet.
细胞表面突起包括富含F-肌动蛋白的波浪状褶皱,这些褶皱会在受到刺激时以及细胞迁移过程中短暂竖起。巨噬细胞是先天性免疫细胞,其会持续产生褶皱,在被病原体激活的细胞中褶皱更为明显。背侧褶皱及其产生的巨吞饮小泡是环境采样、病原体检测和免疫信号传导的关键部位。对褶皱进行定量评估对于评估巨噬细胞对病原体的反应以及分析其他细胞类型对生长因子的反应很重要,但目前缺乏自动化的定量方法,主要依靠手动和定性评估。在此,我们展示了一个用于从3D显微镜图像中定量背侧细胞表面突起的自动化ImageJ宏程序。本文介绍的检测方法适用于高通量筛选应用,通过测量褶皱面积和强度并在易于阅读的组合电子表格中提供标准化值,来检测药物、病原体或生长因子诱导的细胞褶皱变化。