Koonce M P, Schliwa M
J Cell Biol. 1986 Aug;103(2):605-12. doi: 10.1083/jcb.103.2.605.
The peripheral feeding network of the giant freshwater ameba Reticulomyxa can be easily and rapidly lysed to produce an extensive, stable, and completely exposed cytoskeletal framework of colinear microtubules and microfilaments. Most of the organelles that remain attached to this framework resume rapid saltatory movements at rates of up to 20 micron/s if ATP is added. This lysed model system is also capable of other forms of motility, namely an active splaying of microtubule bundles and bulk streaming. Reactivation does not occur with other nucleoside triphosphates, requires Mg ions, is insensitive to even high concentrations of erythro-9-(3-[2-hydroxynonyl]) adenine, is sensitive to vanadate only at concentrations of approximately 100 microM, and is inhibited by N-ethylmaleimide at concentrations greater than 100 microM. The physiology of this reactivation suggests an organelle transport motor distinct from cytoplasmic dynein and possibly the recently described kinesin. This system can serve as a model for elucidating the mechanisms of intracellular transport and, in addition, provides a unique opportunity to examine associations between microtubules and microfilaments.
大型淡水变形虫网状变形虫(Reticulomyxa)的外周供能网络可以很容易且快速地被裂解,从而产生一个由共线微管和微丝组成的广泛、稳定且完全暴露的细胞骨架框架。如果添加ATP,大多数附着在该框架上的细胞器会以高达20微米/秒的速度恢复快速跳跃运动。这个裂解后的模型系统还能够进行其他形式的运动,即微管束的主动展开和整体流动。其他核苷三磷酸不会引发再激活,再激活需要镁离子,即使在高浓度的erythro-9-(3-[2-羟基壬基])腺嘌呤存在下也不敏感,仅在浓度约为100微摩尔时对钒酸盐敏感,并且在浓度大于100微摩尔时会被N-乙基马来酰亚胺抑制。这种再激活的生理学现象表明存在一种不同于细胞质动力蛋白且可能不同于最近描述的驱动蛋白的细胞器运输马达。该系统可作为阐明细胞内运输机制的模型,此外,还提供了一个独特的机会来研究微管和微丝之间的关联。