Watanabe H, Miake K, Sasaki J
Departments of Histology, Tokyo Dental College, Chiba City, Japan.
Acta Anat (Basel). 1993;147(1):14-23.
We evaluated the cytoskeleton of osteoblasts in the rat calvaria by transmission electron microscopy after perfusion with a mixture of Triton X-100 and glutaraldehyde and immunoelectron microscopy. In osteoblasts, microfilaments (5-6 nm in diameter) and intermediate filaments (10-12 nm) were arranged in networks or bundles, avoiding cell organelles such as mitochondria and the rough-surfaced endoplasmic reticulum. Some of these intermediate filaments were attached to the nucleus and had a double-helix structure. Immunoelectron microscopy demonstrated that these fibers are actin and vimentin filaments, respectively. Intermediate filaments were abundant around the nucleus while microfilaments were abundant around the cell membrane. Microfilaments formed thick bundles around the cell membrane in formative osteoblasts but did not form bundles in resting osteoblasts.
在用Triton X-100和戊二醛混合液灌注及免疫电子显微镜检查后,我们通过透射电子显微镜评估了大鼠颅骨成骨细胞的细胞骨架。在成骨细胞中,微丝(直径5 - 6纳米)和中间丝(10 - 12纳米)呈网络状或束状排列,避开了线粒体和糙面内质网等细胞器。其中一些中间丝附着于细胞核,具有双螺旋结构。免疫电子显微镜显示这些纤维分别是肌动蛋白丝和波形蛋白丝。中间丝在细胞核周围丰富,而微丝在细胞膜周围丰富。在形成期成骨细胞中,微丝在细胞膜周围形成粗束,而在静止期成骨细胞中不形成束。