Meyer J M, Staubli A, Ruch J V
Cell Tissue Res. 1981;220(3):589-97. doi: 10.1007/BF00216762.
Ruthenium red staining and tannic acid fixation were used to analyse the fine structure of embryonic mouse dental basement membrane in intact first mandibular molars or in EDTA-isolated dental papillae. Preameloblasts are separated from extracellular matrix proper by a basal lamina that contains regularly arranged proteoglycan granules of about 10 nm in diameter. This distribution pattern is particularly evident in the inner and outer lamina rara of the basal lamina associated with EDTA-isolated dental papillae. The plasmalemma of preameloblasts demonstrates electron dense plaques on the inner leaflet. Ruthenium red positive granules (50 nm in diameter) coat nonstriated and striated fibrils of the matrix. Hyaluronidase treatment digested the ruthenium red positive granules. Tannic acid fixation allowed the demonstration of filaments within the lamina rara interna, connecting the lamina densa with plasmalemma of preameloblasts. These observations are discussed in the context of the terminal differentiation of odontoblasts.
采用钌红染色和单宁酸固定法,分析完整的第一下颌磨牙或经乙二胺四乙酸(EDTA)分离的牙乳头中胚胎小鼠牙基底膜的精细结构。前成釉细胞通过一层基膜与细胞外基质本体分离,该基膜含有直径约10纳米、排列规则的蛋白聚糖颗粒。这种分布模式在与EDTA分离的牙乳头相关的基膜的内、外透明层中尤为明显。前成釉细胞的质膜在内小叶上显示出电子致密斑。钌红阳性颗粒(直径50纳米)覆盖基质的无横纹和有横纹纤维。透明质酸酶处理可消化钌红阳性颗粒。单宁酸固定可显示内透明层内的细丝,这些细丝将致密层与前成釉细胞的质膜相连。结合成牙本质细胞的终末分化对这些观察结果进行了讨论。