Wilson Timothy, Parikka Vilhelmiina, Holmbom Johanna, Ylänen Heimo, Penttinen Risto
Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, FIN 20520 Turku, Finland.
J Biomed Mater Res A. 2006 Apr;77(1):67-74. doi: 10.1002/jbm.a.30600.
Bioactive glass reacts with body fluids and is gradually dissolved in tissues and in cell cultures. We investigated whether osteoclasts contribute to this process, by culturing newborn rat bone-marrow cells containing osteoclasts on polished bioactive glass plates (glass S53P4). The cultures were inspected at days 1-5 and stained for alkaline phosphatase (ALP) to demonstrate osteoblasts and for tartrate resistant acid phosphatase (TRAP) to visualize osteoclasts. Nonosteoclastic cells proliferated several-fold both on bioactive glass and on plastic, whereas osteoclasts and their precursors matured into multicellular giant cells and degenerated. Most cells on bioactive glass became ALP-positive, whereas on plastic the majority of cells remained ALP-negative. Osteoclasts survived on bioactive glass for 4-5 days, whereas on plastic they degenerated and disappeared after 3 days. Condensed nuclei indicating apoptosis were detected both in degenerating osteoclasts and osteoblasts. The surface of the bioactive glass reacted rapidly forming rounded pits, erosions, and cracks within 24 h in areas occupied by osteoblasts. Light microscopy and scanning electron micrographs demonstrated, however, a smooth surface below the cytoplasm of osteoclasts. This indicates that when applied on an intact bioactive glass surface, osteoclasts were unable to dissolve the glass material within this culture period.
生物活性玻璃与体液发生反应,并在组织和细胞培养物中逐渐溶解。我们通过在抛光的生物活性玻璃板(玻璃S53P4)上培养含有破骨细胞的新生大鼠骨髓细胞,研究破骨细胞是否参与了这一过程。在第1至5天对培养物进行检查,并用碱性磷酸酶(ALP)染色以显示成骨细胞,用抗酒石酸酸性磷酸酶(TRAP)染色以观察破骨细胞。非破骨细胞在生物活性玻璃和塑料上均增殖了数倍,而破骨细胞及其前体则成熟为多核巨细胞并发生退化。生物活性玻璃上的大多数细胞变为ALP阳性,而在塑料上,大多数细胞仍为ALP阴性。破骨细胞在生物活性玻璃上存活4至5天,而在塑料上,它们在3天后退化并消失。在退化的破骨细胞和成骨细胞中均检测到指示凋亡的浓缩核。生物活性玻璃表面在24小时内迅速发生反应,在成骨细胞占据的区域形成圆形凹坑、侵蚀和裂缝。然而,光学显微镜和扫描电子显微镜照片显示,破骨细胞细胞质下方的表面是光滑的。这表明当应用于完整的生物活性玻璃表面时,破骨细胞在该培养期内无法溶解玻璃材料。