BioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
BioMediTech, Tampere University of Technology, Tampere, Finland.
Commun Biol. 2020 Oct 2;3(1):548. doi: 10.1038/s42003-020-01273-w.
Development and study of cell-cultured constructs, such as tissue-engineering scaffolds or organ-on-a-chip platforms require a comprehensive, representative view on the cells inside the used materials. However, common characteristics of biomedical materials, for example, in porous, fibrous, rough-surfaced, and composite materials, can severely disturb low-energy imaging. In order to image and quantify cell structures in optically challenging samples, we combined labeling, 3D X-ray imaging, and in silico processing into a methodological pipeline. Cell-structure images were acquired by a tube-source X-ray microtomography device and compared to optical references for assessing the visual and quantitative accuracy. The spatial coverage of the X-ray imaging was demonstrated by investigating stem-cell nuclei inside clinically relevant-sized tissue-engineering scaffolds (5x13 mm) that were difficult to examine with the optical methods. Our results highlight the potential of the readily available X-ray microtomography devices that can be used to thoroughly study relative large cell-cultured samples with microscopic 3D accuracy.
细胞培养构建体(如组织工程支架或芯片上器官平台)的开发和研究需要对所用材料内部的细胞进行全面、有代表性的观察。然而,生物医学材料的常见特性,例如多孔、纤维状、粗糙表面和复合材料,会严重干扰低能量成像。为了对具有挑战性的光学样本中的细胞结构进行成像和定量分析,我们将标记、3D X 射线成像和计算机处理结合到一个方法学管道中。通过管源 X 射线微断层成像设备获取细胞结构图像,并与光学参考图像进行比较,以评估视觉和定量准确性。通过研究临床相关尺寸的组织工程支架(5x13mm)内的干细胞核,证明了 X 射线成像的空间覆盖范围,这些支架用光学方法很难进行检查。我们的结果突出了现成的 X 射线微断层成像设备的潜力,这些设备可用于彻底研究具有微观 3D 精度的相对较大的细胞培养样本。