Dugina V B, Svitkina T M, Vasiliev J M, Gelfand I M
Proc Natl Acad Sci U S A. 1987 Jun;84(12):4122-5. doi: 10.1073/pnas.84.12.4122.
The phorbol ester phorbol 12-myristate 13-acetate (PMA) induced reversible alteration of the shape of fibroblastic cells of certain transformed lines--namely, partition of the cells into two types of domains: motile body actively extending large lamellas and stable narrow cytoplasmic processes. Dynamic observations have shown that stable processes are formed from partially retracted lamellas and from contracted tail parts of cell bodies. Immunofluorescence microscopy and electron microscopy of platinum replicas of cytoskeleton have shown that PMA-induced narrow processes are rich in microtubules and intermediate filaments but relatively poor in actin microfilaments; in contrast, lamellas and cell bodies contained numerous microfilaments. Colcemid-induced depolymerization of microtubules led to contraction of PMA-induced processes; cytochalasin B prevented this contraction. It is suggested that PMA-induced separation of cell into motile and stable parts is due to directional movement of actin structures along the microtubular framework. Similar movements may play an important role in various normal morphogenetic processes.
佛波酯佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)可诱导某些转化细胞系的成纤维细胞形状发生可逆改变,即将细胞分为两种类型的结构域:活跃伸展大伪足的活动体和稳定的狭窄细胞质突起。动态观察表明,稳定的突起由部分回缩的伪足和细胞体收缩的尾部形成。免疫荧光显微镜检查和细胞骨架铂复制品的电子显微镜检查表明,PMA诱导的狭窄突起富含微管和中间丝,但肌动蛋白微丝相对较少;相反,伪足和细胞体含有大量微丝。秋水仙酰胺诱导的微管解聚导致PMA诱导的突起收缩;细胞松弛素B可阻止这种收缩。有人认为,PMA诱导的细胞分为活动部分和稳定部分是由于肌动蛋白结构沿微管框架的定向运动。类似的运动可能在各种正常形态发生过程中起重要作用。