Takahashi H
Department of Anatomy, Hirosaki University School of Medicine, Japan.
Anat Embryol (Berl). 1988;178(4):353-8. doi: 10.1007/BF00698666.
Cell surface carbohydrates in the neurulating ectoderm of bantam chick embryos of stage 6-11 were examined using the fluorescein isothiocyanate-labeled and ferritin-labeled peanut lectin, Arachis hypogaea agglutinin (PNA), which is Gal beta 1----3GalNAc specific. Weak fluorescence showing PNA binding sites was seen on the apical surfaces of neural plate cells. On the surfaces of neural tube cells the fluorescence was more intense and appeared as a band. When using ferritin particles as a quantitative EM marker, only a few PNA binding sites covering the apical surfaces of the basal plate cells during the neural plate stage were seen (274.3 +/- 18.67 ferritin particles/micron 2). As neural tube formation advanced, the number of the ferritin labeled PNA binding sites increased as was to be expected from the fluorescent label experiment. At the neural ridge contact stage there were 2.5 times more binding sites than at the neural plate stage. After this period, the lectin binding sites showed no significant changes. These results were the inverse of those for RCAI or WGA lectins previously reported by us. These observations suggest that sugar residues or the sugar-chain skeletons on the neuroectoderm are altered during neurulation.
使用异硫氰酸荧光素标记和铁蛋白标记的花生凝集素(Arachis hypogaea agglutinin,PNA),其对Galβ1----3GalNAc具有特异性,对6-11期矮脚鸡胚胎神经胚形成期外胚层的细胞表面碳水化合物进行了检测。在神经板细胞的顶端表面可见显示PNA结合位点的微弱荧光。在神经管细胞表面,荧光更强,呈带状。当使用铁蛋白颗粒作为定量电镜标记时,在神经板阶段仅可见少数覆盖基板细胞顶端表面的PNA结合位点(274.3±18.67个铁蛋白颗粒/微米²)。随着神经管形成的推进,铁蛋白标记的PNA结合位点数量增加,这与荧光标记实验预期的结果一致。在神经嵴接触阶段,结合位点比神经板阶段多2.5倍。在此之后,凝集素结合位点没有显著变化。这些结果与我们之前报道的RCAI或WGA凝集素的结果相反。这些观察结果表明,神经外胚层上的糖残基或糖链骨架在神经胚形成过程中发生了改变。