Frotscher M, Léránth C
J Comp Neurol. 1986 Jan 1;243(1):58-70. doi: 10.1002/cne.902430106.
A monoclonal antibody against choline acetyltransferase (ChAT), the acetylcholine-synthesizing enzyme, was used to study cholinergic synapses on identified (Golgi stained) granule cells in the rat fascia dentata. Choline acetyltransferase immunocytochemistry was applied to 40-microns Vibratome sections cut perpendicular to the longitudinal axis of the hippocampus. Light microscopy revealed fine varicose ChAT-immunoreactive axons in all layers of the fascia dentata, i.e., in the stratum moleculare, the stratum granulosum, and the subgranular polymorph zone. Most fibers were observed in the vicinity of granule cell bodies where they ran mainly parallel to the granular layer. Next, the immunostained Vibratome sections were sandwiched between small pieces of Parafilm and piled to form a block that was covered with agar and Golgi stained. After that, the sections were separated by cutting away the agar and removing the Parafilm. Sections containing well-impregnated granule cells were gold-toned (Fairén et al., '77), embedded in Araldite, and subjected to ultrathin sectioning for electron microscopy. A total of 14 gold-toned granule cells were examined in the electron microscope for synaptic contacts with cholinergic afferents. Choline acetyltransferase-immunoreactive axon terminals were observed that established symmetric synaptic contacts with the cell bodies and dendritic shafts of the gold-toned identified granule cells. Two types of contact were observed on spines arising from gold-toned granule cell dendrites. Immunoreactive terminals established asymmetric synaptic contacts with the head of small spines and symmetric contacts with the stalk of large, complex spines. The boutons forming asymmetric synaptic contacts with the cup-shaped spine head of the complex spines were not found to be immunoreactive. Our results demonstrate that cholinergic fibers to the rat fascia dentata establish characteristic types of synaptic contact with different postsynaptic elements of granule cells, suggesting a complex function of this afferent system.
一种针对胆碱乙酰转移酶(ChAT,合成乙酰胆碱的酶)的单克隆抗体被用于研究大鼠齿状回中已鉴定(经高尔基染色)的颗粒细胞上的胆碱能突触。胆碱乙酰转移酶免疫细胞化学技术应用于垂直于海马体长轴切割的40微米振动切片。光学显微镜显示,在齿状回的所有层中,即分子层、颗粒层和颗粒下多形区,都有细小的曲张状ChAT免疫反应性轴突。大多数纤维在颗粒细胞体附近被观察到,它们主要平行于颗粒层分布。接下来,将免疫染色的振动切片夹在小块保鲜膜之间,堆积形成一个用琼脂覆盖并进行高尔基染色的块。之后,通过切掉琼脂并去除保鲜膜来分离切片。含有充分浸染颗粒细胞的切片进行金染色(法伦等人,1977年),嵌入环氧树脂中,并进行超薄切片用于电子显微镜观察。在电子显微镜下总共检查了14个金染色的颗粒细胞与胆碱能传入纤维的突触联系。观察到胆碱乙酰转移酶免疫反应性轴突终末与金染色的已鉴定颗粒细胞的细胞体和树突干建立了对称突触联系。在金染色颗粒细胞树突产生的棘突上观察到两种类型的接触。免疫反应性终末与小棘突的头部建立了不对称突触联系,与大的复杂棘突的柄部建立了对称联系。未发现与复杂棘突杯状棘突头部形成不对称突触联系的终扣具有免疫反应性。我们的结果表明,大鼠齿状回的胆碱能纤维与颗粒细胞的不同突触后成分建立了特征性的突触联系类型,提示该传入系统具有复杂的功能。