Kordeli E, Cartaud J, Nghiêm H O, Pradel L A, Dubreuil C, Paulin D, Changeux J P
J Cell Biol. 1986 Mar;102(3):748-61. doi: 10.1083/jcb.102.3.748.
The subcellular distribution of the 43,000-D protein (43 kD or v1) and of some major cytoskeletal proteins was investigated in Torpedo marmorata electrocytes by immunocytochemical methods (immunofluorescence and immunogold at the electron microscope level) on frozen-fixed sections and homogenates of electric tissue. A monoclonal antibody directed against the 43-kD protein (Nghiêm, H. O., J. Cartaud, C. Dubreuil, C. Kordeli, G. Buttin, and J. P. Changeux, 1983, Proc. Natl. Acad. Sci. USA, 80:6403-6407), selectively labeled the postsynaptic membrane on its cytoplasmic face. Staining by anti-actin and anti-desmin antibodies appeared evenly distributed within the cytoplasm: anti-desmin antibodies being associated with the network of intermediate-sized filaments that spans the electrocyte, and anti-actin antibodies making scattered clusters throughout the cytoplasm without preferential labeling of the postsynaptic membrane. On the other hand, a dense coating by anti-actin antibodies became apparent on the postsynaptic membrane in homogenates of electric tissue pointing to the possible artifactual redistribution of a soluble cytoplasmic actin pool. Anti-fodrin and anti-ankyrin antibodies selectively labeled the non-innervated membrane of the cell. F actin was also detected in this membrane. Filamin and vinculin, two actin-binding proteins recently localized at the rat neuromuscular junction (Bloch, R. J., and Z. W. Hall, 1983, J. Cell Biol., 97:217-223), were detected in the electrocyte by the immunoblot technique but not by immunocytochemistry. The data are interpreted in terms of the functional polarity of the electrocyte and of the selective interaction of the cytoskeleton with the innervated and non-innervated domains of the plasma membrane.
运用免疫细胞化学方法(在冷冻固定切片及电组织匀浆上进行免疫荧光和电镜水平的免疫金标),研究了电鳐(Torpedo marmorata)电细胞中43,000道尔顿蛋白(43 kD或v1)及一些主要细胞骨架蛋白的亚细胞分布。一种针对43-kD蛋白的单克隆抗体(Nghiêm, H. O., J. Cartaud, C. Dubreuil, C. Kordeli, G. Buttin, and J. P. Changeux, 1983, Proc. Natl. Acad. Sci. USA, 80:6403 - 6407),选择性地标记了突触后膜的胞质面。抗肌动蛋白和抗结蛋白抗体的染色在细胞质内呈均匀分布:抗结蛋白抗体与横跨电细胞的中等大小纤维网络相关,而抗肌动蛋白抗体在整个细胞质中形成散在的簇,未对突触后膜进行优先标记。另一方面,在电组织匀浆的突触后膜上,抗肌动蛋白抗体形成致密包被,这表明可溶性胞质肌动蛋白池可能出现人为的重新分布。抗血影蛋白和抗锚蛋白抗体选择性地标记了细胞的非神经支配膜。在该膜中也检测到了F肌动蛋白。通过免疫印迹技术在电细胞中检测到了细丝蛋白和纽蛋白这两种最近定位于大鼠神经肌肉接头处的肌动蛋白结合蛋白(Bloch, R. J., and Z. W. Hall, 1983, J. Cell Biol., 97:217 - 223),但未通过免疫细胞化学方法检测到。这些数据从电细胞的功能极性以及细胞骨架与质膜神经支配和非神经支配区域的选择性相互作用方面进行了解释。