Zagoren J C, Raine C S, Suzuki K
Brain Res. 1982 Jun 17;242(1):19-25. doi: 10.1016/0006-8993(82)90491-7.
Cations are known to bind to the node of Ranvier and the paranodal regions of myelinated fibers. The integrity of these specialized structures is essential for normal conduction. Sites of cation binding can be microscopically identified by the electrondense histochemical reaction product formed by the precipitate of copper sulfate/potassium ferrocyanide. This technique was used to study the distribution of cation binding during normal development of myelinating fibers. Sciatic nerves of C57B1 mice, at 1, 3, 5, 6, 7, 8, 9, 13, 16, 18, 24 and 30 days of age, were prepared for electron microscopy following fixation in phosphate-buffered 2.5% glutaraldehyde and 1% osmic acid, microdissection and incubation in phosphate-buffered 0.1 M cupric sulfate followed by 0.1 M potassium ferrocyanide. Localization of reaction product was studied by light and electron microscopy. By light microscopy, no reaction product was observed prior to 9 days of age. At 13 days, a few nodes and paranodes exhibited reaction product. This increased in frequency and intensity up to 30 days when almost all nodes or paranodes exhibited reaction product. Ultrastructurally, diffuse reaction product was first observed at 3 days of age in the axoplasm of the node, in the paranodal extracellular space of the terminal loops, in the Schwann cell proper and in the terminal loops of Schwann cell cytoplasm. When myelinated axons fulfilled the criteria for mature nodes, reaction product was no longer observed in the Schwann cell cytoplasm, while the intensity of reaction product in the nodal axoplasm and paranodal extracellular space of the terminal loops increased. Reaction product in the latter site appeared to be interrupted by the transverse bands. These results suggest that cation binding accompanies nodal maturity and that the Schwann cell may play a role in production or storage of the cation binding substance during myelinogenesis and development.
已知阳离子会结合到郎飞结和有髓纤维的旁结区域。这些特殊结构的完整性对于正常传导至关重要。阳离子结合位点可通过硫酸铜/亚铁氰化钾沉淀形成的电子致密组织化学反应产物在显微镜下进行识别。该技术用于研究有髓纤维正常发育过程中阳离子结合的分布情况。将不同日龄(1、3、5、6、7、8、9、13、16、18、24和30日龄)的C57B1小鼠坐骨神经,在磷酸盐缓冲的2.5%戊二醛和1%锇酸中固定、显微解剖,然后在磷酸盐缓冲的0.1 M硫酸铜中孵育,接着在0.1 M亚铁氰化钾中孵育,之后制备用于电子显微镜观察的样本。通过光学显微镜和电子显微镜研究反应产物的定位。光学显微镜观察发现,9日龄之前未观察到反应产物。13日龄时,少数结和旁结出现反应产物。直至30日龄,反应产物的频率和强度不断增加,此时几乎所有的结或旁结都出现了反应产物。超微结构观察显示,3日龄时在结的轴质、终末袢的旁结细胞外间隙、雪旺细胞本体以及雪旺细胞细胞质的终末袢中首次观察到弥漫性反应产物。当有髓轴突达到成熟结的标准时,雪旺细胞细胞质中不再观察到反应产物,而结的轴质和终末袢的旁结细胞外间隙中的反应产物强度增加。后一部位的反应产物似乎被横向带中断。这些结果表明阳离子结合伴随着结的成熟,并且雪旺细胞可能在髓鞘形成和发育过程中参与阳离子结合物质的产生或储存。