Ushiki T, Shigeno M, Abe K
Department of Anatomy, Hokkaido University School of Medicine, Sapporo, Japan.
Arch Histol Cytol. 1994 Oct;57(4):427-32. doi: 10.1679/aohc.57.427.
The atomic force microscope (AFM) was applied for the first time to embedment-free biological sections. Aldehyde-fixed tissues (kidney, liver etc.) of mice were postfixed with osmium tetroxide and cut into 500-700 nm thick sections after embedding of the tissue block in polyethylene glycol (PEG); the sections mounted on glass slides were deembedded and critical point-dried. The AFM images were collected in air from those tissue sections in a dynamic force mode. Solid-height-mode images, which were comparable to transmission electron microscope (TEM) images, seemed to provide us more useful information than the solid-mode images which resembled scanning electron microscope (SEM) images. Internal structures including chromatin fibers in the nuclei and cytoplasmic organelles were clearly recognizable by AFM. Minute surface structures including the end-feet of renal podocytes were demonstrated. We confirm that a vertical resolution of 0.1 nm and a lateral resolution of 5-10 nm are attainable with the dynamic force mode of AFM using thin sections of tissues. The present paper proposes the usefulness of AFM for observation of biological materials without metal coating in a non-vacuous environment.
原子力显微镜(AFM)首次应用于无包埋生物切片。将小鼠的醛固定组织(肾脏、肝脏等)用四氧化锇后固定,在将组织块包埋于聚乙二醇(PEG)中后切成500 - 700纳米厚的切片;将安装在载玻片上的切片进行脱包埋处理并临界点干燥。在空气中以动态力模式从这些组织切片采集AFM图像。与透射电子显微镜(TEM)图像可比的固体高度模式图像,似乎比类似于扫描电子显微镜(SEM)图像的固体模式图像为我们提供了更多有用信息。AFM能够清晰识别包括细胞核中的染色质纤维和细胞质细胞器在内的内部结构。展示了包括肾足细胞终末足在内的微小表面结构。我们证实,使用组织薄片,AFM的动态力模式可实现0.1纳米的垂直分辨率和5 - 10纳米的横向分辨率。本文提出了AFM在非真空环境下无需金属镀膜观察生物材料的实用性。