μ-VIS X-ray Imaging Centre, Faculty of Engineering and Physical Sciences, University of Southampton, Southampton, United Kingdom.
Biomedical Imaging Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Am J Pathol. 2019 Aug;189(8):1608-1620. doi: 10.1016/j.ajpath.2019.05.004. Epub 2019 May 22.
Historically, micro-computed tomography (μCT) has been considered unsuitable for histologic analysis of unstained formalin-fixed, paraffin-embedded soft tissue biopsy specimens because of a lack of image contrast between the tissue and the paraffin. However, we recently demonstrated that μCT can successfully resolve microstructural detail in routinely prepared tissue specimens. Herein, we illustrate how μCT imaging of standard formalin-fixed, paraffin-embedded biopsy specimens can be seamlessly integrated into conventional histology workflows, enabling nondestructive three-dimensional (3D) X-ray histology, the use and benefits of which we showcase for the exemplar of human lung biopsy specimens. This technology advancement was achieved through manufacturing a first-of-kind μCT scanner for X-ray histology and developing optimized imaging protocols, which do not require any additional sample preparation. 3D X-ray histology allows for nondestructive 3D imaging of tissue microstructure, resolving structural connectivity and heterogeneity of complex tissue networks, such as the vascular network or the respiratory tract. We also demonstrate that 3D X-ray histology can yield consistent and reproducible image quality, enabling quantitative assessment of a tissue's 3D microstructures, which is inaccessible to conventional two-dimensional histology. Being nondestructive, the technique does not interfere with histology workflows, permitting subsequent tissue characterization by means of conventional light microscopy-based histology, immunohistochemistry, and immunofluorescence. 3D X-ray histology can be readily applied to a plethora of archival materials, yielding unprecedented opportunities in diagnosis and research of disease.
从历史上看,由于组织与石蜡之间缺乏图像对比度,微计算机断层扫描 (μCT) 一直被认为不适合对未经染色的福尔马林固定、石蜡包埋的软组织活检标本进行组织学分析。然而,我们最近证明 μCT 可以成功解析常规制备的组织标本中的微观结构细节。本文介绍了如何将标准福尔马林固定、石蜡包埋的活检标本的 μCT 成像无缝集成到常规组织学工作流程中,实现无损三维 (3D) X 射线组织学,展示了这种技术在人类肺活检标本中的应用和优势。这一技术进步是通过制造首例用于 X 射线组织学的 μCT 扫描仪以及开发优化的成像方案实现的,这些方案不需要任何额外的样品制备。3D X 射线组织学允许对组织微观结构进行无损 3D 成像,解析复杂组织网络(如血管网络或呼吸道)的结构连接和异质性。我们还证明 3D X 射线组织学可以产生一致且可重复的图像质量,从而能够对组织的 3D 微观结构进行定量评估,而这是传统二维组织学无法实现的。由于该技术是无损的,因此不会干扰组织学工作流程,允许随后通过基于传统的光镜的组织学、免疫组织化学和免疫荧光对组织进行特征分析。3D X 射线组织学可以很容易地应用于大量的存档材料,为疾病的诊断和研究提供了前所未有的机会。