Niggemann B, Maaser K, Lü H, Kroczek R, Zänker K S, Friedl P
Institute of Immunology, University Witten/Herdecke, Witten, Germany.
Cancer Lett. 1997 Oct 14;118(2):173-80. doi: 10.1016/s0304-3835(97)00328-5.
Active cellular locomotion is a feature of such diverse cell types as lymphocytes and cancer cells. The locomotory phenotype of a cell should ultimately reflect the biochemical basis of different migratory strategies. We investigated the locomotory behavior of five epithelial cell lines and one non-epithelial human cell-line as well as human CD4+ T lymphocytes in a three-dimensional collagen type I matrix using time-lapse video microscopy and computer assisted cell-tracking. Migration velocity was up to 70 times lower in tumor cells (0.1-0.3 microm/min) as compared to T lymphocytes (7-7.5 microm/min), whereas the percentage of spontaneously active cells was up to twice as high in tumor cells (80-90%) in comparison to T lymphocytes (54%). Persistence, i.e. the degree of roaming, varied appreciably between the different cell types. In conclusion, velocity and persistence may describe distinct migration strategies in different cell types, i.e. discerning T cell migration from tumor cell invasion.
活跃的细胞运动是淋巴细胞和癌细胞等多种不同细胞类型的一个特征。细胞的运动表型最终应反映不同迁移策略的生化基础。我们使用延时视频显微镜和计算机辅助细胞追踪技术,研究了五种上皮细胞系、一种非上皮人类细胞系以及人类CD4 + T淋巴细胞在三维I型胶原基质中的运动行为。与T淋巴细胞(7 - 7.5微米/分钟)相比,肿瘤细胞的迁移速度低至70倍(0.1 - 0.3微米/分钟),而肿瘤细胞中自发活跃细胞的百分比是T淋巴细胞(54%)的两倍(80 - 90%)。持续性,即漫游程度,在不同细胞类型之间有明显差异。总之,速度和持续性可能描述了不同细胞类型中的不同迁移策略,即区分T细胞迁移和肿瘤细胞侵袭。