Jones G E
J Cell Sci. 1975 Mar;17(3):371-9. doi: 10.1242/jcs.17.3.371.
Over a concentration range of o-5-10 mug/cm-3, cytochalasin B caused a biphasic change in the electrophoretic mobility of disaggregated neural retina cells. An initial rise in anodal mobility at low concentrations of the drug was transformed into a reduction in the mobility below that of the control at a concentration of 10 mug/cm-3. The effect of cytochalasin B was found to be reversible by washing treated cells in cytochalasin B-free media. This was investigated at a concentration of cytochalasin at which the greatest difference existed between the mobilities of the control and experimental cell suspensions. Reaggregation of cell dispersions failed to show any significant difference in the rate of aggregation between cytochalasin B-treated cells and the control. Scanning electron microscopy of cells fixed while in suspension also showed little significant change in the surface morphology upon application of cytochalasin B. In high concentrations of the drug cells appeared somewhat smoother in outline, but no correlation was found between changes in surface morphology and the variations in cell electrophoretic mobility. It is concluded that the observed changes in electrophoretic mobility may be attributed to a binding of cytochalasin B to the cell membrane. This lends support to the hypothesis that the primary site of action of cytochalasin B may be the plasma membrane.
在浓度范围为0.5 - 10微克/立方厘米时,细胞松弛素B导致解离的神经视网膜细胞的电泳迁移率发生双相变化。在低浓度药物作用下,阳极迁移率最初上升,而在药物浓度达到10微克/立方厘米时,迁移率降至低于对照水平。通过在不含细胞松弛素B的培养基中洗涤处理过的细胞,发现细胞松弛素B的作用是可逆的。这是在细胞松弛素浓度处于对照和实验细胞悬液迁移率差异最大时进行研究的。细胞分散体的重新聚集显示,细胞松弛素B处理的细胞与对照之间在聚集速率上没有任何显著差异。对悬浮状态下固定的细胞进行扫描电子显微镜观察,结果也表明,施加细胞松弛素B后细胞表面形态几乎没有显著变化。在高浓度药物作用下,细胞轮廓显得有些更光滑,但未发现表面形态变化与细胞电泳迁移率变化之间存在相关性。得出的结论是,观察到的电泳迁移率变化可能归因于细胞松弛素B与细胞膜的结合。这支持了细胞松弛素B的主要作用位点可能是质膜的假说。