Godman G, Woda B, Kolberg R, Berl S
Eur J Cell Biol. 1980 Oct;22(2):745-54.
In HeLa and HEp2, cell lines derived from human carcinoma, application of cytochalasin D (CD) is followed in minutes by generalized cell contraction and zeiosis. Simultaneously, actin, myosin and tropomyosin, mostly from cables, become relocated in condensed masses. Most of these occupy the bases of the zeiotic knobs protruding at the cell surface. In contrast to most nontransformed cell types, in these cells both the protrusions and the contractile proteins are concomitantly translocated centripetally to the cell apex to form an aggregate of zeiotic knobs and a subjacent, membrane-associated, actin-based microfilamentous cap containing tropomyosin and myosin. The redistribution of these contractile proteins is antagonized by pretreatment with inhibitors of energy metabolism, or with cyclic adenine nucleotide. The centripetal movement appears to be guided by microtubules, which tend a radiate toward apical aggregates. Under the influence of CD 10 nm filaments associate in bundles. These processes are rapidly reversed after withdrawal of CD. The changes in distribution of actin, myosin and tropomyosin in relation to cell surface structures are considered in terms of the hypothesis that CD induces contraction of the microfilament apparatus of the cortex which, at least in part, remains tethered to plasma membrane.
在源自人类癌组织的HeLa和HEp2细胞系中,应用细胞松弛素D(CD)几分钟后,细胞会出现普遍收缩和形成泡状突起。同时,肌动蛋白、肌球蛋白和原肌球蛋白(大多来自微丝束)会重新定位到浓缩的团块中。其中大部分占据了细胞表面突出的泡状突起的基部。与大多数未转化的细胞类型不同,在这些细胞中,突起和收缩蛋白会同时向心迁移到细胞顶端,形成泡状突起的聚集体以及下方与膜相关的、基于肌动蛋白的微丝帽,其中含有原肌球蛋白和肌球蛋白。这些收缩蛋白的重新分布会被能量代谢抑制剂或环腺苷酸预处理所拮抗。向心运动似乎由微管引导,微管倾向于向顶端聚集体辐射。在CD的影响下,10纳米的细丝会束状聚集。去除CD后,这些过程会迅速逆转。肌动蛋白、肌球蛋白和原肌球蛋白分布相对于细胞表面结构的变化,是根据CD诱导皮质微丝装置收缩这一假说进行考虑的,该装置至少部分仍与质膜相连。