Brückner G, Müller L, Wollweber L, Samtleben R, Biesold D
J Hirnforsch. 1985;26(6):615-34.
The location of lectin binding sites and of anionic components was studied in the embryonic rat cerebral cortex after the formation of the cortical plate at embryonic day 18. The cortical layers advanced in differentiation, i.e. the sub-plate region and the marginal zone, showed a predominant staining with peroxidase conjugates of wheat germ agglutinin (WGA), peanut agglutinin (PNA), and after immunocytochemical detection of PNA binding sites. This pattern was obtained also with the colloidal iron hydroxide staining method. In contrast to this, the binding of concanavalin A and of succinylated WGA did not reveal a prevalent staining of the sub-plate region and the marginal zone. The further histochemical analysis of the substances responsible for the selective staining of these layers was performed by lipid extractions and by enzymatic treatment of the tissue sections with trypsin, hyaluronidase or neuraminidase prior to the binding of lectins or colloidal iron. The results obtained indicated high concentrations of sialylated galactosylglycoproteins in coexistence with glycosaminoglycans. Electron microscopy was performed with peroxidase conjugates of WGA and PNA. Binding sites of both of the lectins in the sub-plate region and in the marginal zone were located mainly at cell surfaces of the different cellular structures. The most intensive binding of WGA and PNA was detected at the surface membranes and at intracellular material of amoeboid microglial cells and astrocyte-like cell processes. It can be concluded that in distinct brain areas during early differentiation specific glycoproteins in coexistence with glycosaminoglycans are situated at, or associated with cell surfaces in high concentrations. The identical histochemical features previously described in mesenchymal tissues suggest that these glycoconjugates might be related to common morphogenetic processes in which non-neuronal cells of brain and body are specifically involved.
在胚胎第18天形成皮质板后,研究了凝集素结合位点和阴离子成分在胚胎大鼠大脑皮质中的定位。皮质层在分化过程中,即亚板区和边缘区,在用小麦胚芽凝集素(WGA)、花生凝集素(PNA)的过氧化物酶结合物以及免疫细胞化学检测PNA结合位点后,显示出主要的染色。用氢氧化铁胶体染色法也得到了这种模式。与此相反,伴刀豆球蛋白A和琥珀酰化WGA的结合并未显示亚板区和边缘区有普遍的染色。在凝集素或胶体铁结合之前,通过脂质提取以及用胰蛋白酶、透明质酸酶或神经氨酸酶对组织切片进行酶处理,对导致这些层选择性染色的物质进行了进一步的组织化学分析。所得结果表明,唾液酸化半乳糖基糖蛋白与糖胺聚糖共存,且浓度较高。用WGA和PNA的过氧化物酶结合物进行了电子显微镜检查。亚板区和边缘区这两种凝集素的结合位点主要位于不同细胞结构的细胞表面。在阿米巴样小胶质细胞和星形胶质细胞样细胞突起的表面膜和细胞内物质处检测到WGA和PNA的结合最为强烈。可以得出结论,在早期分化过程中,不同的脑区中,特定的糖蛋白与糖胺聚糖共存,且高浓度地位于细胞表面或与细胞表面相关。先前在间充质组织中描述的相同组织化学特征表明,这些糖缀合物可能与共同的形态发生过程有关,在这些过程中,脑和身体的非神经元细胞特别参与其中。