Department of Pathology, Erasmus Medical Center, Rotterdam, The Netherlands.
J Cell Physiol. 2014 Aug;229(8):967-73. doi: 10.1002/jcp.24538.
The detection of co-localization of immunohistochemical markers in tissues or cells requires the application of the confocal laser scanning microscope (CLSM) to multiple immunofluorescence (MIF) stainings. CLSM is operationally sophisticated but requires time-consuming procedures of imaging and reconstruction, and a professional operator is required for manipulation of the microscopic system. Therefore, this technique is less suitable for the examination of many samples in a short time. Moreover, the technique only allows imaging of selected areas of a sample at one time and is not practical for fast panoramic mapping and tracking of whole tissue sections. Here we show a powerful high-throughput and operationally simple histological approach using the Hamamatsu NDP slide scanner (Hamamatsu Nanozoomer 2.0HT) and its viewing platform (NDP.Viewer). The approach not only enables fast mapping and tracking of overlapping spots or regions stained with multiple markers, but also offers panoramic screening of whole tissue sections with fully electronic manipulation for the visualization and analysis of any individual regions.
在组织或细胞中检测免疫组织化学标记物的共定位需要应用共聚焦激光扫描显微镜(CLSM)对多重免疫荧光(MIF)染色进行分析。CLSM 操作复杂,但需要耗时的成像和重建过程,并且需要专业操作人员来操作显微镜系统。因此,该技术不太适合在短时间内检查大量样本。此外,该技术一次只能对样本的选定区域进行成像,不适合快速全景映射和跟踪整个组织切片。在这里,我们展示了一种使用 Hamamatsu NDP 幻灯片扫描仪(Hamamatsu Nanozoomer 2.0HT)及其观察平台(NDP.Viewer)的强大高通量且操作简单的组织学方法。该方法不仅能够快速映射和跟踪用多种标记物染色的重叠斑点或区域,还能够对整个组织切片进行全景筛选,并且可以进行全电子操作,以可视化和分析任何单个区域。