Wang S M, Chen J S, Fong T H, Wu J C
Department of Anatomy, College of Medicine, National Taiwan University, Taipei.
Histochem J. 1996 Jul;28(7):469-76. doi: 10.1007/BF02331406.
Using a xanthophore cytoskeletal preparation as immunogen, we have produced a monoclonal antibody, A2, which recognized a 160 kDa protein in 3T3 fibroblasts. This protein makes up a cytoplasmic filamentous system, which colocalizes with vimentin filaments. When microtubules and actin filaments are dissolved by high salt extraction, staining with antibody A2 is unaffected. Immunoblot analysis confirms that the 160 kDa protein is co-isolated with vimentin during in vivo high salt extraction. Following vinblastine treatment, both the 160 kDa protein and vimentin become localized to perinuclear caps, as do other intermediate filaments and their associated proteins; after vinblastine removal, the immunostaining produced by A2 becomes filamentous. Immunoelectron microscopy demonstrates that antibody A2 stains a filament system with a diameter of about 10 nm. Our observations suggest that the 160 kDa protein may be a new vimentin-associated protein which differs from the intermediate filament-associated proteins previously reported, and is widely distributed in several cell types.
以黄色素细胞骨架制剂作为免疫原,我们制备了一种单克隆抗体A2,它能识别3T3成纤维细胞中的一种160 kDa蛋白。这种蛋白构成了一个细胞质丝状系统,与波形蛋白丝共定位。当微管和肌动蛋白丝通过高盐提取被溶解时,用抗体A2染色不受影响。免疫印迹分析证实,在体内高盐提取过程中,160 kDa蛋白与波形蛋白共分离。在用长春花碱处理后,160 kDa蛋白和波形蛋白都定位于核周帽,其他中间丝及其相关蛋白也是如此;去除长春花碱后,A2产生的免疫染色变为丝状。免疫电子显微镜显示,抗体A2染色的丝状系统直径约为10 nm。我们的观察结果表明,160 kDa蛋白可能是一种新的波形蛋白相关蛋白,它不同于先前报道的中间丝相关蛋白,并且广泛分布于几种细胞类型中。