Gritsaenko Tatiana, Pierrefite-Carle Valérie, Creff Gaëlle, Vidaud Claude, Carle Georges, Santucci-Darmanin Sabine
UMR E-4320 TIRO-MATOs CEA/DRF/BIAM, Université Nice Sophia-Antipolis.
UMR 7272 Institut de Chimie de Nice CNRS, Université Nice Sophia-Antipolis.
J Vis Exp. 2018 Jan 30(131):56499. doi: 10.3791/56499.
Uranium has been shown to interfere with bone physiology and it is well established that this metal accumulates in bone. However, little is known about the effect of natural uranium on the behavior of bone cells. In particular, the impact of uranium on osteoclasts, the cells responsible for the resorption of the bone matrix, is not documented. To investigate this issue, we have established a new protocol using uranyl acetate as a source of natural uranium and the murine RAW 264.7 cell line as a model of osteoclast precursors. Herein, we detailed all the assays required to test uranium cytotoxicity on osteoclast precursors and to evaluate its impact on the osteoclastogenesis and on the resorbing function of mature osteoclasts. The conditions we have developed, in particular for the preparation of uranyl-containing culture media and for the seeding of RAW 264.7 cells allow to obtain reliable and highly reproductive results. Moreover, we have optimized the use of software tools to facilitate the analysis of various parameters such as the size of osteoclasts or the percentage of resorbed matrix.
铀已被证明会干扰骨骼生理,并且这种金属在骨骼中积累已得到充分证实。然而,关于天然铀对骨细胞行为的影响却知之甚少。特别是,铀对破骨细胞(负责骨基质吸收的细胞)的影响尚无文献记载。为了研究这个问题,我们建立了一种新方案,使用醋酸铀酰作为天然铀的来源,并使用小鼠RAW 264.7细胞系作为破骨细胞前体的模型。在此,我们详细介绍了测试铀对破骨细胞前体的细胞毒性以及评估其对破骨细胞生成和成熟破骨细胞吸收功能影响所需的所有检测方法。我们所建立的条件,特别是用于制备含铀培养基和接种RAW 264.7细胞的条件,能够获得可靠且高度可重复的结果。此外,我们优化了软件工具的使用,以方便对各种参数进行分析,如破骨细胞的大小或吸收基质的百分比。