Uchida Kazuhiko S K, Yumura Shigehiko
Department of Biology, Faculty of Science, Yamaguchi University, Yamaguchi 753-8512, Japan.
J Cell Sci. 2004 Mar 15;117(Pt 8):1443-55. doi: 10.1242/jcs.01015.
We observed the dynamics of actin foci in live Dictyostelium cells expressing GFP-actin. Actin foci were dynamic structures, but they were fixed on the substratum during cell migration. Interference reflection microscopy revealed that the ventral cell membrane was closer to the substratum at sites of actin foci. Furthermore, some actin foci were incorporated into the retraction fibers, ripped off from the cells and eventually shed on the substratum after the cells moved away. The velocity of the cells was inversely proportional to the number of actin foci. Measurement of traction force using a silicone substratum demonstrated that the traction force was transmitted to the substratum through actin foci. Taken together, several lines of evidence strongly suggest that actin foci function as the active 'feet' of Dictyostelium cells. We also found evidence suggesting that changing step is regulated in a coordinated manner during cell migration. Possible mechanisms by which these cells migrate across substrata are discussed in this context.
我们观察了表达绿色荧光蛋白(GFP)-肌动蛋白的活盘基网柄菌细胞中肌动蛋白焦点的动态变化。肌动蛋白焦点是动态结构,但在细胞迁移过程中它们固定在基质上。干涉反射显微镜显示,在肌动蛋白焦点部位,细胞腹侧细胞膜更靠近基质。此外,一些肌动蛋白焦点被整合到收缩纤维中,从细胞上撕下,最终在细胞移开后留在基质上。细胞速度与肌动蛋白焦点数量成反比。使用硅酮基质测量牵引力表明,牵引力通过肌动蛋白焦点传递到基质上。综上所述,多条证据有力地表明,肌动蛋白焦点起着盘基网柄菌细胞活跃“脚”的作用。我们还发现有证据表明,在细胞迁移过程中,步长变化是以协调的方式调节的。在此背景下讨论了这些细胞穿过基质迁移的可能机制。