Fukui Y, Uyeda T Q, Kitayama C, Inoué S
Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611-3008, USA.
Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10020-5. doi: 10.1073/pnas.97.18.10020.
We report here our efforts to measure the crawling force generated by cells undergoing amoeboid locomotion. In a centrifuge microscope, acceleration was increased until amoebae of Dictyostelium discoideum were "stalled" or no longer able to "climb up." The "apparent weight" of the amoebae at stalling rpm in myosin mutants depended on the presence of myosin II (but not myosins IA and IB) and paralleled the cortical strength of the cells. Surprisingly, however, the cell stalled not only in low-density media as expected but also in media with densities greater than the cell density where the buoyant force should push the amoeba upward. We find that the leading pseudopod is bent under centrifugal force in all stalled amoebae, suggesting that this pseudopod is very dense indeed. This finding also suggests that directional cell locomotion against resistive forces requires a turgid forward-pointing pseudopod, most likely sustained by cortical actomyosin II.
我们在此报告我们为测量进行阿米巴样运动的细胞所产生的爬行力而做出的努力。在离心显微镜中,不断增加加速度,直到盘基网柄菌的变形虫“停滞”或不再能够“向上攀爬”。在肌球蛋白突变体中,处于停滞转速时变形虫的“表观重量”取决于肌球蛋白II(而非肌球蛋白IA和IB)的存在,并与细胞的皮质强度平行。然而,令人惊讶的是,细胞不仅如预期那样在低密度培养基中停滞,而且在密度大于细胞密度的培养基中也会停滞,在这种情况下浮力应将变形虫向上推。我们发现,在所有停滞的变形虫中,领先伪足在离心力作用下会弯曲,这表明该伪足确实非常致密。这一发现还表明,细胞对抗阻力的定向运动需要一个肿胀的向前伸出的伪足,很可能由皮质肌动球蛋白II维持。