Brands R, de Boer A, Feltkamp C A, Roos E
Division of Cell Biology, The Netherlands Cancer Institute (Antoni van Leeuwenhoek Huis), Amsterdam.
Exp Cell Res. 1990 Jan;186(1):138-48. doi: 10.1016/0014-4827(90)90220-5.
The localization of talin and vinculin in chicken embryo fibroblasts (CEF) during transformation was studied by immunoelectron microscopy. CEF cells were infected with a temperature-sensitive mutant of Rous sarcoma virus. After 16 h at 42 degrees C, transformation was induced by incubation at 37 degrees C for different intervals up to 3 h. Cells were cleaved by "wet cleaving" as reported previously by us (R. Brands and C.A. Feltkamp, 1988, Exp. Cell Res. 176, 309) and labeled with affinity-purified polyclonal antibodies to talin or vinculin, or monoclonal anti-vinculin. We observed a rapid reduction of vinculin in adhesion plaques within 15 min and a much slower dissociation of talin. This was found using single-labeling procedures and also within the same cell using double labeling. Seemingly intact microfilament bundles were observed associated with adhesion plaques that contained relatively little vinculin. These observations show that an early event in src-induced transformation is the release of vinculin from adhesion plaques. Furthermore, since adhesion plaques with attached filament bundles can exist at least transiently with very little or no vinculin present, it seems likely that vinculin is not, or not the only protein, linking actin filaments to adhesion plaques.
通过免疫电子显微镜研究了鸡胚成纤维细胞(CEF)在转化过程中踝蛋白和纽蛋白的定位。用劳斯肉瘤病毒的温度敏感突变体感染CEF细胞。在42℃下培养16小时后,在37℃下孵育不同时间(最长3小时)诱导转化。按照我们之前报道的方法(R. Brands和C.A. Feltkamp,1988,《细胞实验研究》176,309)通过“湿裂解”裂解细胞,并用针对踝蛋白或纽蛋白的亲和纯化多克隆抗体或抗纽蛋白单克隆抗体进行标记。我们观察到,在15分钟内黏着斑中的纽蛋白迅速减少,而踝蛋白的解离则慢得多。这是通过单标记程序观察到的,并且在同一细胞内使用双标记也观察到了。观察到看似完整的微丝束与黏着斑相关,而这些黏着斑中纽蛋白相对较少。这些观察结果表明,src诱导的转化中的一个早期事件是纽蛋白从黏着斑中释放。此外,由于带有附着的细丝束的黏着斑至少可以短暂存在,其中纽蛋白含量极少或不存在,因此纽蛋白似乎不是或将不是将肌动蛋白丝连接到黏着斑的唯一蛋白质。