Pierce A M, Lindskog S, Hammarström L
Department of Dentistry, University of Adelaide, Australia.
Electron Microsc Rev. 1991;4(1):1-45. doi: 10.1016/0892-0354(91)90015-5.
Osteoclasts are multinucleated giant cells showing specialized membrane structures, clear zones and ruffled borders, which are responsible for the process of bone resorption. These cells arrive at the resorption site via the bloodstream as mononuclear cells, derived from haemopoietic precursors in the spleen or bone marrow, which fuse prior to resorption. The osteoclast may share an early progenitor cell, the granulocyte macrophage colony-forming unit (GM-CFU) with monocytes, macrophages and granulocytes, implying that osteoclasts share the pluripotent haemopoietic stem cell with all other haemopoietic cells. In the past, elucidation of the structure of these cells relied upon traditional ultrastructural techniques. Transmission electron microscopic studies revealed details of the unique ultrastructure of these cells and, in combination with stereological techniques, showed the response of cells to various hormonal stimuli. Scanning electron microscopy not only demonstrated the surface appearance of osteoclasts, and their predilection for spreading on various substratum components, but has also been used as an adjunct in resorption assays in which areas of resorption lacunae are measured as indicators of cell activity. Recent advances in fields such as immunocytochemistry and freeze fracture techniques have contributed towards a more detailed delineation of antigenic profile, cytoskeletal structure and localization of enzymatic pathways. The osteoclast is subject to extensive regulatory mechanisms and it has been established that the osteoblast plays a major rôle in mediating the effects of osteotropic hormones and local mediators on these cells. Hence, research aimed at elucidating the coupling mechanisms between these two cells may result in new therapies for bone disease.
破骨细胞是具有特殊膜结构、透明区和皱褶缘的多核巨细胞,负责骨吸收过程。这些细胞以单核细胞的形式通过血液循环到达吸收部位,单核细胞来源于脾脏或骨髓中的造血前体,在吸收前融合。破骨细胞可能与单核细胞、巨噬细胞和粒细胞共享早期祖细胞,即粒细胞巨噬细胞集落形成单位(GM-CFU),这意味着破骨细胞与所有其他造血细胞共享多能造血干细胞。过去,这些细胞结构的阐明依赖于传统的超微结构技术。透射电子显微镜研究揭示了这些细胞独特超微结构的细节,并结合体视学技术,显示了细胞对各种激素刺激的反应。扫描电子显微镜不仅展示了破骨细胞的表面外观及其在各种基质成分上的铺展倾向,还被用作吸收测定的辅助手段,在该测定中,吸收陷窝的面积被测量作为细胞活性的指标。免疫细胞化学和冷冻断裂技术等领域的最新进展有助于更详细地描绘抗原谱、细胞骨架结构和酶途径的定位。破骨细胞受到广泛的调节机制影响,并且已经确定成骨细胞在介导促骨激素和局部介质对这些细胞的作用中起主要作用。因此,旨在阐明这两种细胞之间偶联机制的研究可能会带来治疗骨疾病的新方法。