Confocal assay for invasion: use of propidium iodide fluorescence and laser reflectance to quantify the rate of migration of cells through a matrix.

Cytometry Pub Date : 2000-08-01
U Benbow, K A Orndorff, C E Brinckerhoff, A L Givan
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Abstract

Background: Most assays used to measure invasion are based on manual counting of the number of cells that have migrated completely through commercial coated filters. We describe here a confocal fluorescence-imaging method that can assess the relative rates of invasion of cells into a matrix.

Methods: After being seeded on the matrix and a period of incubation, the cells are fixed and treated with RNase. Propidium iodide is then added to stain the double-stranded DNA. A confocal microscope system is used to obtain high-resolution images of the red propidium iodide fluorescence and laser reflectance from optical sections at increasing depths in the matrix. The section with high laser reflectance marks the top of the matrix.

Results: Data were calculated as the total area of red fluorescence above background in each section and were plotted as a percentage of the summed fluorescent areas in all sections.

Conclusions: Because the distance into the matrix of the nuclei can be calculated by measuring from the reflective upper surface of the matrix, the method is useful for assessing the rate of cell migration and for comparing the ability of different cells to invade through different matrices under varying conditions.

侵袭共聚焦测定:使用碘化丙啶荧光和激光反射来量化细胞通过基质的迁移率。
背景:大多数用于测量入侵的检测方法是基于人工计数通过商业包被过滤器完全迁移的细胞数量。我们在这里描述了一种共聚焦荧光成像方法,可以评估细胞侵入基质的相对率。方法:细胞接种于基质上孵育一段时间后,固定细胞,用RNase处理。然后加入碘化丙啶染色双链DNA。共聚焦显微镜系统用于获得高分辨率图像的红色碘化丙啶荧光和激光反射率的光学切片在增加深度的矩阵。激光反射率高的部分标记在矩阵的顶部。结果:数据计算为每个切片中背景上方红色荧光的总面积,并绘制为所有切片中荧光面积总和的百分比。结论:由于可以从基质的反射上表面测量细胞核进入基质的距离,因此该方法可用于评估细胞迁移速率和比较不同条件下不同细胞通过不同基质的入侵能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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