Gruppo San Donato Foundation, Milan, Italy.
Cell Tissue Res. 2012 Oct;350(1):69-75. doi: 10.1007/s00441-012-1436-2. Epub 2012 Jun 7.
Fish scale culture can be used as a model to test the effects of several molecules on bone metabolism by histological and biochemical methods, although solid cell biology data about the behavior of the scale cells in culture are needed if such a model is to be employed for pharmacological applications. In the present study, we cultured zebrafish scales at various temperatures and for various times and analyzed the behavior of the bone cells in terms of viability and activity. We demonstrated that the cultured scale cells maintained their usual distribution at 28°C until 72 h, after which time episquamal osteoblasts showed an obvious change in their cell organization followed by an increase in cell death. Osteoclast tartrate-resistant acid phosphatase and osteoblast alkaline phosphatase activities were maintained until 72 h but were reduced at 96 h as a consequence of the massive cell death. This scenario indicates that zebrafish scales cultured until 72 h can be considered as an innovative model of explanted organ culture to assay the ability of chemical compounds to modulate the metabolism of bone cells.
鱼类鳞片培养可以通过组织学和生化方法来测试几种分子对骨代谢的影响,尽管如果要将这种模型用于药理学应用,则需要有关鳞片细胞在培养中行为的可靠细胞生物学数据。在本研究中,我们在不同温度下和不同时间培养斑马鱼鳞片,并根据细胞活力和活性分析骨细胞的行为。我们证明,培养的鳞片细胞在 28°C 下保持其通常的分布,直到 72 小时后,表皮成骨细胞的细胞组织发生明显变化,随后细胞死亡增加。破骨细胞抗酒石酸酸性磷酸酶和成骨细胞碱性磷酸酶活性可维持至 72 小时,但由于大量细胞死亡,在 96 小时时降低。这种情况表明,培养至 72 小时的斑马鱼鳞片可以被认为是一种创新的离体器官培养模型,用于测定化学化合物调节骨细胞代谢的能力。