Soueidan A, Gan O I, Gouin F, Godard A, Heymann D, Jacques Y, Daculsi G
Laboratoire de Recherche sur les Materiaux d'Intéret Biologique CNRS-INSERM, Faculté de Chirurgie Dentaire, Nantes, France.
Virchows Arch. 1995;426(5):469-77. doi: 10.1007/BF00193170.
Osteoclastic cells from giant cell tumour of bone (GCT) of bone provide a rich source for investigation of cellular mechanisms leading to formation of multinucleated cells, the resorption process and involvement of hormones and cytokines in these events. In the present study we investigated the effect of 1,25-dihydroxyvitamin D3 (VD3) and leukaemia inhibitory factor (LIF) on the resorbing potential of osteoclast of GCT origin using quantitative image-analysis of resorption lacunae in an in vitro dentine model. While VD3 unsignificantly increased the number of resorption pits and implicated surface after 7 days of GCT cell culturing, the stimulative effect of LIF was statistically significant. In cultures supplemented with LIF (5000 U/ml) the number of lacunae and resorption surface increased by 38% and 55%, respectively, when compared with control cultures. We suggest that both osteotropic agents increased osteoclastic activity, as the number of multinucleated cells was similar in control and experimental cultures. Seeding of GCT cells on biphasic calcium phosphate substratum revealed the relative inability of osteoclastic cells to resorb this synthetic material.
骨巨细胞瘤(GCT)中的破骨细胞为研究导致多核细胞形成的细胞机制、吸收过程以及激素和细胞因子在这些事件中的作用提供了丰富的来源。在本研究中,我们使用体外牙本质模型中吸收陷窝的定量图像分析,研究了1,25 - 二羟基维生素D3(VD3)和白血病抑制因子(LIF)对GCT来源破骨细胞吸收潜能的影响。在GCT细胞培养7天后,VD3对吸收凹坑数量和牵连表面的增加作用不显著,而LIF的刺激作用具有统计学意义。与对照培养相比,在添加LIF(5000 U/ml)的培养物中,陷窝数量和吸收表面分别增加了38%和55%。我们认为这两种促骨剂均增加了破骨细胞活性,因为对照培养和实验培养中多核细胞的数量相似。将GCT细胞接种在双相磷酸钙基质上显示破骨细胞相对无法吸收这种合成材料。