Katsuma Y, Marceau N, Ohta M, French S W
Department of Pathology, Faculty of Health Sciences, University of Ottawa, Canada.
Hepatology. 1988 May-Jun;8(3):559-68. doi: 10.1002/hep.1840080321.
A new method of visualizing the three-dimensional architecture of the cytokeratin filaments of the intact rat hepatocyte in situ has been achieved. Frozen sections of liver cut 10 micron thick were serially extracted to remove all elements of the cells except the intermediate filaments. Parallel sections were stained with monoclonal antibodies to the two main cytokeratins found in bile duct and liver cells. Immunofluorescent antibody and immunogold electron microscopy techniques were used to identify the proteins morphologically. Several new observations resulted from these studies. The pericanalicular sheath of intermediate filaments was visualized using steropairs as an uninterrupted branching tubular structure composed of cytokeratins located in the cell cortex of adjacent hepatocytes. Intermediate filaments in the cell cortex formed a distinct sheet of matted filaments which enveloped the entire hepatocyte. The cortical intermediate filaments were in continuity with the pericanalicular sheath and the filaments located within the cytoplasm. The intermediate filaments are attached to the centrioles and appeared to tent the nuclear lamina-pore complex at points of contact. Monoclonal antibodies to rat liver intermediate filament cytokeratins (CK49 and CK55) each stained intermediate filaments located in the cell cortex, within the cytoplasm and at the nucleus. By immunogold staining, some of the intermediate filament filaments were shown to contain both cytokeratins. Filaments which did not stain were thought to be either actin at the cell periphery or nuclear lamins around the nucleus. It is concluded that the cytokeratins form a specialized framework for the cell cortex, canaliculus, centrioles and the nucleus of hepatocytes. The filaments run continuously throughout the cytoplasm without terminating.
已实现一种可视化完整大鼠肝细胞原位细胞角蛋白丝三维结构的新方法。将肝脏切成10微米厚的冰冻切片进行连续抽提,以去除细胞中除中间丝以外的所有成分。平行切片用针对胆管和肝细胞中发现的两种主要细胞角蛋白的单克隆抗体进行染色。采用免疫荧光抗体和免疫金电子显微镜技术从形态学上鉴定这些蛋白质。这些研究产生了一些新的观察结果。使用立体对观察到中间丝的胆小管周围鞘,其为位于相邻肝细胞细胞皮质中的细胞角蛋白组成的不间断分支管状结构。细胞皮质中的中间丝形成了一层明显的交织丝,包裹着整个肝细胞。皮质中间丝与胆小管周围鞘以及位于细胞质内的丝相连。中间丝附着于中心粒,并在接触点处似乎使核纤层 - 孔复合体呈帐篷状。针对大鼠肝脏中间丝细胞角蛋白(CK49和CK55)的单克隆抗体分别对位于细胞皮质、细胞质和细胞核中的中间丝进行染色。通过免疫金染色,一些中间丝显示同时含有两种细胞角蛋白。未染色的丝被认为要么是细胞周边的肌动蛋白,要么是细胞核周围的核纤层蛋白。结论是,细胞角蛋白为肝细胞的细胞皮质、胆小管、中心粒和细胞核形成了一个特殊的框架。这些丝在整个细胞质中连续延伸而不终止。