Minkin C
Calcif Tissue Int. 1982 May;34(3):285-90. doi: 10.1007/BF02411252.
Organ cultures of newborn mouse calvaria were used to test the hypothesis that tartrate-resistant acid phosphatase might serve as a biochemical marker for osteoclast function. When bone resorption was stimulated in vitro with either parathyroid hormone or 1,25(OH)2D3, there was a significant increase in both tartrate-resistant and tartrate-sensitivity acid phosphatase activity in the medium relative to cultured controls. Tartrate-resistant activity was localized histochemically primarily over the osteoclast and appeared as three distinct activity bands when electrophoresed on polyacrylamide gels. The tartrate-sensitive activity was found primarily associated with bone cells other than the osteoclast using histochemical techniques, and was resolved into five bands on polyacrylamide gels. The results obtained from biochemical assays, histochemical observations, and polyacrylamide gel electrophoresis suggest that bone resorption in vitro results in the release of tartrate-resistant acid phosphatase from osteoclasts and tartrate-sensitive acid phosphatase from other bone cells as well as osteoclasts. Tartrate-resistant acid phosphatases of bone may be suitable biochemical probes for osteoclasts function, but it will be necessary to achieve further purification in order to develop analytical methods with sufficient sensitivity and specificity (e.g., immunochemical) to ensure precise localization and quantitation.
抗酒石酸酸性磷酸酶可能作为破骨细胞功能的生化标志物。当用甲状旁腺激素或1,25(OH)₂D₃在体外刺激骨吸收时,相对于培养对照,培养基中抗酒石酸和对酒石酸敏感的酸性磷酸酶活性均显著增加。抗酒石酸活性通过组织化学方法主要定位在破骨细胞上,在聚丙烯酰胺凝胶上电泳时呈现为三条不同的活性带。使用组织化学技术发现,对酒石酸敏感的活性主要与破骨细胞以外的骨细胞相关,在聚丙烯酰胺凝胶上可解析为五条带。生化测定、组织化学观察和聚丙烯酰胺凝胶电泳的结果表明,体外骨吸收导致抗酒石酸酸性磷酸酶从破骨细胞中释放出来,同时对酒石酸敏感的酸性磷酸酶也从其他骨细胞以及破骨细胞中释放出来。骨的抗酒石酸酸性磷酸酶可能是用于破骨细胞功能的合适生化探针,但为了开发具有足够灵敏度和特异性的分析方法(例如免疫化学方法)以确保精确定位和定量,有必要进一步纯化。