Tannenbaum J, Godman G C
Mol Cell Biol. 1983 Jan;3(1):132-42. doi: 10.1128/mcb.3.1.132-142.1983.
In HEp-2 cells treated with 0.2 to 2.0 microM cytochalasin D (CD) for 7.5 to 24 h there was a 20 to 50% relative increase in actin content (units of actin per microgram of total cell protein). This augmentation, which was concentration and time dependent, was prevented by treatment with cycloheximide during exposure to CD. A 15 to 20% increase in the relative rate of actin synthesis in CD-treated HEp-2 cells (0.2 to 2.0 microM CD) was detectable after 1 h of treatment and increased to 30 to 50% by 24 h. This increased rate of actin synthesis was apparently responsible for the higher actin content of CD-treated HEp-2 cells. The concentration dependence of these effects of CD on actin metabolism correlated with the pattern seen for CD-triggered changes in cellular morphology and the underlying rearrangements of the actin-containing cytoskeletal structures, suggesting that the effects on metabolism and morphology were interrelated. Since the rapidly occurring cytoskeletal reorganization preceded the effects of CD on actin metabolism, it is proposed that actin synthesis is induced by the cytoskeletal rearrangement resulting from exposure to CD.
在用0.2至2.0微摩尔细胞松弛素D(CD)处理7.5至24小时的HEp - 2细胞中,肌动蛋白含量(每微克总细胞蛋白中的肌动蛋白单位)相对增加了20%至50%。这种增加具有浓度和时间依赖性,在暴露于CD期间用环己酰亚胺处理可阻止其发生。在处理1小时后,可检测到用CD处理的HEp - 2细胞(0.2至2.0微摩尔CD)中肌动蛋白合成相对速率增加了15%至20%,到24小时时增加到30%至50%。肌动蛋白合成速率的增加显然是用CD处理的HEp - 2细胞中肌动蛋白含量较高的原因。CD对肌动蛋白代谢的这些作用的浓度依赖性与CD引发的细胞形态变化模式以及含肌动蛋白的细胞骨架结构的潜在重排相关,这表明对代谢和形态的影响是相互关联的。由于快速发生的细胞骨架重组先于CD对肌动蛋白代谢的影响,因此有人提出肌动蛋白合成是由暴露于CD导致的细胞骨架重排所诱导的。