Niki T, Saito S, Gladish D K
Image Processing Section, MikiOn, LLC , Tokyo , Japan.
Department of Biology, Miami University , Hamilton , Ohio , USA.
Biotech Histochem. 2019 Oct;94(7):522-526. doi: 10.1080/10520295.2019.1601769. Epub 2019 May 2.
We developed a novel sectioning and staining method to make high contrast, high resolution sections of plant tissue for light microscopy. Specimens of teosinte ( L., ssp. ) root tips were fixed and embedded in Technovit 7100™ plastic resin. Thin sections, 1-2.5 μm, were cut and mounted on glass slides. The sections were either treated with RNase or not, then stained with 0.1% toluidine blue O and observed through ∞/0 objective lenses. For light microscopy, the enzyme staining procedure increased resolution and contrast. High magnification ∞/0 objective lenses produced high quality images for digital photography without using a coverslip or immersion oil. Our slide preparation and microscopic analysis were less labor intensive and more rapid than previous methods and enabled rapid and precise alignment of serial transverse sections for both tracking cell lineages and tissue measurements.
我们开发了一种新颖的切片和染色方法,用于制作用于光学显微镜观察的植物组织高对比度、高分辨率切片。大刍草(L.,亚种)根尖标本经固定后嵌入Technovit 7100™ 塑料树脂中。切成1 - 2.5微米的薄片,并安装在载玻片上。切片要么用核糖核酸酶处理,要么不处理,然后用0.1%的甲苯胺蓝O染色,并通过无限远/0物镜观察。对于光学显微镜观察,酶染色程序提高了分辨率和对比度。高放大倍数的无限远/0物镜无需使用盖玻片或浸油即可生成用于数码摄影的高质量图像。我们的载玻片制备和显微镜分析比以前的方法劳动强度更低、速度更快,并且能够快速、精确地对齐连续横切片,用于追踪细胞谱系和组织测量。