Iwasaki Shin-ichi, Aoyagi Hidekazu, Asami Tomoichiro
Advanced Research Center, The Nippon Dental University School of Life Dentistry at Niigata, 1-8 Hamaura-cho, Niigata 951-8580, Japan.
Odontology. 2006 Sep;94(1):64-8. doi: 10.1007/s10266-005-0059-4.
We examined the expression of keratin 18 (K18), by immunofluorescence staining, while monitoring morphological changes in the periderm on the lingual epithelium of rats by laser-scanning microscopy of epoxy resin-embedded, semi-ultrathin sections. We also examined differential interference contrast (DIC) images of the same sections to define the histology and morphology of the cells. It is difficult to visualize histological details of the fetal lingual epithelium of the rat on semi-ultrathin sections by light microscopy after immunohistochemical staining, because the histological structures in such sections cannot be distinguished by standard counterstaining. To solve this problem and to visualize keratin 18 (K18), we used a combination of immunofluorescence staining of semi-ultrathin sections and corresponding differential contrast (DIC) images, obtained by laser-scanning microscopy.
我们通过免疫荧光染色检测角蛋白18(K18)的表达,同时利用激光扫描显微镜对环氧树脂包埋的半超薄切片进行观察,监测大鼠舌上皮周皮的形态变化。我们还检查了相同切片的微分干涉差(DIC)图像,以确定细胞的组织学和形态。免疫组织化学染色后,在光镜下很难在半超薄切片上观察到大鼠胎儿舌上皮的组织学细节,因为这些切片中的组织结构无法通过标准复染来区分。为了解决这个问题并可视化角蛋白18(K18),我们将半超薄切片的免疫荧光染色与通过激光扫描显微镜获得的相应微分干涉差(DIC)图像相结合。