Reinholt F P, Widholm S M, Ek-Rylander B, Andersson G
Karolinska Institutet, Department of Pathology, Huddinge University Hospital, Sweden.
J Bone Miner Res. 1990 Oct;5(10):1055-61. doi: 10.1002/jbmr.5650051009.
Osteoclasts are effector cells in bone breakdown, and the active bone resorption is confined to the ruffled border zone of these cells. An acid milieu is maintained in this zone which is probably a prerequisite for bone resorption. Tartrate-resistant acid phosphatase (TRAP) activity has been recognized as a characteristic property of osteoclasts and in several studies proposed as a cytochemical marker of osteoclasts. We have previously isolated and characterized a tartrate-resistant and iron-activated acid ATPase (TrATPase) from rat bone, the enzyme being a member of the TRAP family. In the present study the ultrastructural localization of this enzyme was delineated by employing immunogold technique on low temperature-embedded maxillar rat bone. Intensive immunolabeling was seen on the bone surfaces facing the ruffled border zone while lower amounts of marker were seen in adjacent bone areas, that is, on the bone surfaces facing the clear zone and deeper-into the bone. Within the osteoclasts gold markers were observed mainly in vesicular structures interpreted as lysosomes. Immunolabeling was also observed in the recently described endocytic cells located near osteoblasts and osteoclasts. Also in these cells, the marker was confined to lysosomelike structures. The amount of label in bone facing osteoblasts was low, as was the amount within osteoblasts. Our observation of extracellular localization, in particular accumulation of TrATPase in bone matrix facing the ruffled border area of the osteoclasts, favors the view that the enzyme is exported to areas of active bone resorption, thereby indicating a potential role for the enzyme in this process.
破骨细胞是骨吸收的效应细胞,活跃的骨吸收局限于这些细胞的褶皱边缘区。该区域维持着酸性环境,这可能是骨吸收的一个先决条件。抗酒石酸酸性磷酸酶(TRAP)活性已被认为是破骨细胞的一个特征性特性,并且在多项研究中被提议作为破骨细胞的细胞化学标志物。我们之前从大鼠骨中分离并鉴定了一种抗酒石酸且铁激活的酸性ATP酶(TrATPase),该酶是TRAP家族的一员。在本研究中,通过对低温包埋的大鼠上颌骨应用免疫金技术来描绘该酶的超微结构定位。在面向褶皱边缘区的骨表面观察到强烈的免疫标记,而在相邻的骨区域,即在面向清晰区和骨内部更深位置的骨表面,观察到的标记物较少。在破骨细胞内,金标记主要观察到存在于被解释为溶酶体的泡状结构中。在最近描述的位于成骨细胞和破骨细胞附近的内吞细胞中也观察到了免疫标记。同样在这些细胞中,标记物也局限于溶酶体样结构。面向成骨细胞的骨中的标记量较低,成骨细胞内的标记量也较低。我们对细胞外定位的观察,特别是TrATPase在面向破骨细胞褶皱边缘区的骨基质中的积累,支持了该酶被输出到活跃骨吸收区域的观点,从而表明该酶在这一过程中具有潜在作用。