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In vitro model of bone to facilitate measurement of adhesion forces and super-resolution imaging of osteoclasts

机译:骨的体外模型有助于测量破骨细胞的粘附力和超分辨率成像

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摘要

To elucidate processes in the osteoclastic bone resorption, visualise resorption and related actin reorganisation, a combination of imaging technologies and an applicable in vitro model is needed. Nanosized bone powder from matching species is deposited on any biocompatible surface in order to form a thin, translucent, smooth and elastic representation of injured bone. Osteoclasts cultured on the layer expressed matching morphology to ones cultured on sawed cortical bone slices. Resorption pits were easily identified by reflectance microscopy. The coating allowed actin structures on the bone interface to be visualised with super-resolution microscopy along with a detailed interlinked actin networks and actin branching in conjunction with V-ATPase, dynamin and Arp2/3 at actin patches. Furthermore, we measured the timescale of an adaptive osteoclast adhesion to bone by force spectroscopy experiments on live osteoclasts with bone-coated AFM cantilevers. Utilising the in vitro model and the advanced imaging technologies we localised immunofluorescence signals in respect to bone with high precision and detected resorption at its early stages. Put together, our data supports a cyclic model for resorption in human osteoclasts.
机译:为了阐明破骨细胞骨吸收的过程,可视化吸收和相关的肌动蛋白重组,需要结合成像技术和适用的体外模型。来自匹配物种的纳米尺寸骨粉沉积在任何生物相容性表面上,以形成受伤骨的薄,半透明,光滑和弹性的代表。在该层上培养的破骨细胞的形态与在锯切的皮质骨切片上培养的相匹配。吸收坑很容易通过反射显微镜鉴定。该涂层使骨骼界面上的肌动蛋白结构可以通过超分辨率显微镜以及详细的相互连接的肌动蛋白网络和肌动蛋白分支与肌动蛋白斑处的V-ATPase,动力蛋白和Arp2 / 3结合来可视化。此外,我们通过在带骨涂层AFM悬臂的活破骨细胞上进行力谱实验,测量了适应性破骨细胞粘附于骨的时间尺度。利用体外模型和先进的成像技术,我们可以相对于骨骼精确定位免疫荧光信号,并在早期检测到吸收。综上所述,我们的数据支持人类破骨细胞吸收的循环模型。

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