Advanced Research Center, The Nippon Dental University School of Life Dentistry at Niigata, 1-8 Hamaura-cho, Chuo-ku, Niigata 951-8580, Japan.
Acta Histochem. 2011 Jul;113(4):395-401. doi: 10.1016/j.acthis.2010.03.003. Epub 2010 May 23.
We used fluorescence immunohistochemistry, analysis of differential interference contrast (DIC) images and confocal laser-scanning microscopy in the transmission mode, after staining specimens with toluidine blue, to examine the localization of keratin 13 (K13) and keratin 14 (K14) in the lingual epithelium of fetal and juvenile Sprague-Dawley rats during the prenatal and postnatal morphogenesis of circumvallate papillae. No immunoreactivity specific for K13 and K14 was detected in the lingual epithelium of fetuses on day 15 after conception (E15), at which time the primitive rudiment of the circumvallate papillae was detectable by the thickening of several layers of cuboidal epithelial cells. On E17 and E19, the developing circumvallate papillae were clearly recognizable, consisting of a central papilla and the surrounding sulcus. No immunoreactivity specific for K13 and K14 was evident in the lingual epithelium around these structures at this time. K14-specific immunoreactivity was first detected in the basal layer of the epithelium of the circumvallate papillae on postnatal day 0 (P0) and K13-specific immunoreactivity was detected on P7. Morphogenesis of the circumvallate papillae progressed significantly from P0 to P14, and immunoreactivity specific for K13 and K14 was clearly recognizable after P7. The respective patterns of K13-specific and K14-specific immunoreactivity differed during the development of the circumvallate papillae: K13-specific immunoreactivity was generally evident in cells of the intermediate layer of the epithelium, while K14-specific immunoreactivity was detected in cells of the basal and suprabasal layers. The present results are discussed in the context of the previously determined localization of K13 and K14 in the dorsal epithelium of the anterior part of the rat tongue during its morphogenesis.
我们使用荧光免疫组织化学、微分干涉对比(DIC)图像分析和共聚焦激光扫描显微镜传输模式,在经甲苯胺蓝染色的标本上,研究了角蛋白 13(K13)和角蛋白 14(K14)在 Sprague-Dawley 胎鼠和幼鼠舌背味蕾发生过程中的定位。在受孕后第 15 天(E15)的胎儿舌上皮中,未检测到针对 K13 和 K14 的免疫反应性,此时,通过数层立方上皮细胞的增厚可以检测到原始的轮廓乳头雏形。在 E17 和 E19 时,正在发育的轮廓乳头清晰可辨,由中央乳头和周围的沟组成。此时,这些结构周围的舌上皮中没有明显的 K13 和 K14 特异性免疫反应性。在出生后第 0 天(P0),可以在轮廓乳头上皮的基底层首次检测到 K14 特异性免疫反应性,而在 P7 时可以检测到 K13 特异性免疫反应性。从 P0 到 P14,轮廓乳头的形态发生显著进展,在 P7 后可以清楚地识别出针对 K13 和 K14 的免疫反应性。在轮廓乳头发育过程中,K13 特异性和 K14 特异性免疫反应性的模式不同:K13 特异性免疫反应性通常在上皮的中间层细胞中明显,而 K14 特异性免疫反应性则在基底和超基底细胞中检测到。本研究结果与先前在大鼠舌前背侧上皮的形态发生过程中确定的 K13 和 K14 定位进行了讨论。