Sasaki T, Hong M H, Udagawa N, Moriyama Y
Department of Oral Anatomy, School of Dentistry, Showa University, Tokyo, Japan.
Cell Tissue Res. 1994 Nov;278(2):265-71. doi: 10.1007/BF00414169.
By means of light- and electron-microscopic immunocytochemistry, we have demonstrated the expression of vacuolar H(+)-ATPase in mouse osteoclasts. In fully differentiated osteoclasts, intense immunolabeling was observed along the plasma membranes including those of ruffled borders and associated pale vesicles and vacuoles, whereas those of clear zones and basolateral cell surfaces were entirely free of immunoreaction. Specific expression of vacuolar H(+)-ATPase was also detected over polyribosomes and cisterns of the rough-surfaced endoplasmic reticulum. Multinucleated osteoclastic cells were suspended on dentine slices and cultured for 48 h in the presence or absence of either concanamycin B or bafilomycin A1, specific inhibitors of vacuolar H(+)-ATPase. Morphometric analysis of co-cultured dentine slices with backscattered electron microscopy revealed that both inhibitors strongly reduced the formation of resorption lacunae in a dose-dependent manner. These results suggest that vacuolar H(+)-ATPase is produced in the rough-surfaced endoplasmic reticulum, stored in the membrane vesicles, and transported into the ruffled border membranes of osteoclasts, and that this enzyme plays a key role in the creation of an acidic subosteoclastic microenvironment for the demineralization of co-cultured substrates.
通过光镜和电镜免疫细胞化学方法,我们已证实小鼠破骨细胞中存在液泡型H(+)-ATP酶的表达。在完全分化的破骨细胞中,沿质膜包括皱襞缘、相关淡染小泡和液泡的质膜观察到强烈的免疫标记,而清亮区和基底外侧细胞表面则完全没有免疫反应。在多核糖体和糙面内质网的池上也检测到液泡型H(+)-ATP酶的特异性表达。多核破骨细胞悬浮于牙本质切片上,在存在或不存在液泡型H(+)-ATP酶的特异性抑制剂 concanamycin B 或 bafilomycin A1 的情况下培养48小时。用背散射电子显微镜对共培养的牙本质切片进行形态计量分析表明,两种抑制剂均以剂量依赖方式强烈减少吸收陷窝的形成。这些结果表明,液泡型H(+)-ATP酶在内质网中产生,储存于膜小泡中,并转运至破骨细胞的皱襞缘膜,且该酶在为共培养底物脱矿质作用而形成酸性破骨细胞下微环境中起关键作用。