Chardin H, Septier D, Goldberg M
Laboratoire d'Histologie, Faculté de Chirurgie Dentaire, Montrouge, France.
J Histochem Cytochem. 1990 Jun;38(6):885-94. doi: 10.1177/38.6.2110588.
Using cetylpyridinium chloride (CPC) in glutaraldehyde as fixative, we observed sinuous fiber-like structures 300-500 nm long and 7-14 nm thick in the spaces between the collagen fibers of rat incisor predentin. Small granules and fibrils were also detected. Electron-dense vesicles were seen inside the odontoblast processes. The plasma membrane was irregularly stained with material that adhered to its surface. In demineralized dentin, needle-like structures were seen at the periphery of globular structures which were not stained. Staining the sections with Alcian blue did not greatly improve the visualization of CPC-precipitated glycosaminoglycans. The specificity of staining was assessed on serial sections by selective dissociation of glycosaminoglycan aggregates with 2 M calcium chloride and their digestion by bovine testicular hyaluronidase. The glycosaminoglycans were probably combined with lipids, because treatment of the sections with a chloroform/methanol mixture removed the CPC-induced precipitates from both predentin and dentin.
以十六烷基氯化吡啶(CPC)添加到戊二醛中作为固定剂,我们在大鼠切牙前期牙本质的胶原纤维之间的间隙中观察到了长300 - 500纳米、厚7 - 14纳米的蜿蜒纤维状结构。还检测到了小颗粒和原纤维。在成牙本质细胞突起内可见电子致密小泡。质膜被附着在其表面的物质不规则染色。在脱矿牙本质中,在未染色的球状结构周边可见针状结构。用阿尔辛蓝对切片染色并没有显著改善对CPC沉淀的糖胺聚糖的可视化效果。通过用2M氯化钙选择性解离糖胺聚糖聚集体并用牛睾丸透明质酸酶对其进行消化,在连续切片上评估染色的特异性。这些糖胺聚糖可能与脂质结合,因为用氯仿/甲醇混合物处理切片可去除前期牙本质和牙本质中CPC诱导的沉淀物。