Lapper S R, Smith Y, Sadikot A F, Parent A, Bolam J P
MRC Anatomical Neuropharmacology Unit, Oxford, UK.
Brain Res. 1992 May 15;580(1-2):215-24. doi: 10.1016/0006-8993(92)90947-8.
The cortex projects heavily to the striatum and makes asymmetrical synaptic contact mainly with the spines of medium-sized densely spiny neurones. The possibility exists that corticostriatal terminals also make synaptic contact with classes of striatal interneurones. The primary objective of the present experiment was to determine whether parvalbumin-immunoreactive neurones, which represent a class of GABAergic interneurones in the striatum, also receive a direct synaptic input from corticostriatal fibres. The anterograde tracer biocytin was injected into the motor and premotor cortices of the squirrel monkey (Saimiri sciureus). Following perfuse-fixation, sections of the striatum were processed histochemically to reveal the transported biocytin using an avidin-biotin-peroxidase complex and diaminobenzidine as the chromogen. They were then immunostained to reveal parvalbumin using benzidine dihydrochloride as the chromogen. In both the light and electron microscopes, the morphological features and the afferent synaptic input of the parvalbumin-immunoreactive neurones were similar to those observed in other species. Similarly, the morphology and postsynaptic targets of the corticostriatal terminals were similar to those described in other species. Light microscopic examination revealed that the anterogradely labelled corticostriatal terminals were often in close apposition to the parvalbumin-positive neurones. At the electron microscopic level the biocytin-positive corticostriatal terminals were found to make asymmetrical synaptic contacts mainly with spines. The parvalbumin-positive neurones were seen to have an invaginated nucleus, extensive cytoplasm and relatively few spines. Parvalbumin-immunoreactive dendrites received a dense synaptic input consisting mainly of asymmetric synapses and only a few symmetric synapses. Biocytin-labelled corticostriatal terminals were often seen in asymmetrical synaptic contact with parvalbumin-immunoreactive dendrites. These results show that GABAergic interneurones identified on the basis of parvalbumin immunoreactivity, in addition to the projection neurones of the striatum, are under the direct influence of the cerebral cortex.
皮质大量投射到纹状体,主要与中型密集棘状神经元的棘形成不对称突触联系。皮质纹状体终末也有可能与某些类型的纹状体中间神经元形成突触联系。本实验的主要目的是确定在纹状体中代表一类γ-氨基丁酸能中间神经元的小白蛋白免疫反应性神经元是否也接受来自皮质纹状体纤维的直接突触输入。将顺行示踪剂生物胞素注射到松鼠猴(松鼠猴属)的运动皮质和运动前皮质中。灌注固定后,对纹状体切片进行组织化学处理,使用抗生物素蛋白-生物素-过氧化物酶复合物和二氨基联苯胺作为显色剂来显示转运的生物胞素。然后使用盐酸联苯胺作为显色剂对它们进行免疫染色以显示小白蛋白。在光学显微镜和电子显微镜下,小白蛋白免疫反应性神经元的形态特征和传入突触输入与在其他物种中观察到的相似。同样,皮质纹状体终末的形态和突触后靶点与其他物种中描述的相似。光学显微镜检查显示,顺行标记的皮质纹状体终末常常与小白蛋白阳性神经元紧密相邻。在电子显微镜水平上,发现生物胞素阳性的皮质纹状体终末主要与棘形成不对称突触联系;可见小白蛋白阳性神经元有一个内陷核、丰富的细胞质和相对较少的棘。小白蛋白免疫反应性树突接受密集的突触输入,主要由不对称突触组成,只有少数对称突触。经常可见生物胞素标记的皮质纹状体终末与小白蛋白免疫反应性树突形成不对称突触联系。这些结果表明,基于小白蛋白免疫反应性鉴定出的γ-氨基丁酸能中间神经元,除了纹状体的投射神经元外,也受到大脑皮质的直接影响。