Bernhardt A, Koperski K, Schumacher M, Gelinsky M
Fetscherstr. 42, 01309 Dresden,
Eur Cell Mater. 2017 Jan 18;33:28-42. doi: 10.22203/eCM.v033a03.
Cell-based in vitro resorption assays are an important tool to simulate the in vivo biodegradation of resorbable bone graft materials and to predict their clinical performance. The present study analyses the activity of osteoclast-specific enzymes as potential surrogate measures for classical pit assay, which is not applicable on irregular structured materials. Osteoclasts derived from human peripheral blood mononuclear cells were cultivated on different surfaces: calcium phosphate bone cements (CPC), dentin discs, osteoblast-derived extracellular matrix (ECM) and tissue culture polystyrene as control. Pit formation on the resorbable materials was investigated and correlated with the activity of tartrate resistant acid phosphatase (TRAP), carbonic anhydrase II (CAII) and cathepsin K (CTSK). Furthermore, the relation between intra- and extracellular enzyme activities was examined for TRAP and CTSK during resorption of the different materials. Resorbed area of CPC correlated with intracellular TRAP activity and intracellular CAII activity. Highest resorption was detected at around pH 7.2. Resorbed area on dentin correlated with the extracellular CTSK activity and extracellular TRAP activity and was maximal at around pH 6.8. Osteoclasts cultivated on cell-derived mineralised ECM showed a good correlation between both extracellular TRAP and CTSK activity and the release of calcium ions. Based on these data a different regulation of TRAP and CTSK secretion is hypothesised for the resorption of inorganic calcium phosphate compared to the resorption of collagenous mineralised matrix.
基于细胞的体外吸收试验是模拟可吸收骨移植材料体内生物降解并预测其临床性能的重要工具。本研究分析破骨细胞特异性酶的活性,作为经典蚀斑试验的潜在替代指标,经典蚀斑试验不适用于结构不规则的材料。将源自人外周血单核细胞的破骨细胞培养在不同表面上:磷酸钙骨水泥(CPC)、牙本质圆盘、成骨细胞衍生的细胞外基质(ECM)以及作为对照的组织培养聚苯乙烯。研究了可吸收材料上的蚀斑形成情况,并将其与抗酒石酸酸性磷酸酶(TRAP)、碳酸酐酶II(CAII)和组织蛋白酶K(CTSK)的活性相关联。此外,还检测了不同材料吸收过程中TRAP和CTSK的细胞内和细胞外酶活性之间的关系。CPC的吸收面积与细胞内TRAP活性和细胞内CAII活性相关。在pH约7.2时检测到最高吸收。牙本质上的吸收面积与细胞外CTSK活性和细胞外TRAP活性相关,在pH约6.8时最大。在细胞衍生的矿化ECM上培养的破骨细胞显示细胞外TRAP和CTSK活性与钙离子释放之间具有良好的相关性。基于这些数据,假设与胶原矿化基质的吸收相比,无机磷酸钙的吸收对TRAP和CTSK分泌有不同的调节。