Staiger J F, Zilles K, Freund T F
Institute of Experimental Medicine, Hungarian Academy of Science, Budapest, Hungary.
Eur J Neurosci. 1996 Nov;8(11):2273-85. doi: 10.1111/j.1460-9568.1996.tb01191.x.
The spatial synaptic pattern formed by boutons, originating in the ventroposteromedial thalamic nucleus, with GABAergic neurons in the rat barrel cortex was mapped. The aim was to shed light on the structural basis by which inhibitory circuits may be activated at the first stage of cortical information processing. The thalamic afferent projection was labelled by anterograde transport of Phaseolus vulgaris leucoagglutinin (PHA-L), whereas the GABAergic targets in layer IV of the rat barrel cortex was visualized by postembedding GABA immunogold-labelling or by pre-embedding parvalbumin immunocytochemistry. In the first set of experiments, we mapped barrels, contained in single ultrathin sections, by means of a computer-controlled electron microscope stage in their entire layer IV representation. From a total of 1199 asymmetric PHA-L-labelled synapses, only 98 were on GABAergic elements, mainly on dendritic shafts. This corresponded to 8.2% of all synapses counted. These synapses on GABAergic targets were essentially homogeneously distributed without a reliable relationship to barrel subdivisions, i.e., hollow versus wall; or layer IVa versus layer IVb. In the second part of the study, we demonstrated that parvalbumin-containing neurons represent the major GABAergic cell type targetted by thalamic afferents in layer IV of the barrel cortex, since all parvalbumin-positive cells investigated received multiple synaptic contacts (up to eight synapses per neuron) from the ventroposteromedial thalamic nucleus. These results imply that interneurons responsible for perisomatic inhibition (basket and chandelier cells known to contain parvalbumin) are likely to be strongly excited by thalamic afferents, despite the relatively low proportion of thalamic synapses on GABAergic elements compared to spines of principal cells, and participate in the early stages of cortical sensory information processing.
绘制了起源于丘脑腹后内侧核的终扣与大鼠桶状皮质中γ-氨基丁酸能神经元形成的空间突触模式。目的是阐明在皮质信息处理的第一阶段抑制性回路可能被激活的结构基础。通过菜豆白细胞凝集素(PHA-L)的顺行运输标记丘脑传入投射,而通过包埋后γ-氨基丁酸免疫金标记或包埋前小白蛋白免疫细胞化学来观察大鼠桶状皮质IV层中的γ-氨基丁酸能靶点。在第一组实验中,我们借助计算机控制的电子显微镜载物台,在其整个IV层代表区域内绘制单个超薄切片中的桶状结构。在总共1199个不对称PHA-L标记的突触中,只有98个位于γ-氨基丁酸能元件上,主要在树突干上。这相当于所有计数突触的8.2%。这些位于γ-氨基丁酸能靶点上的突触基本均匀分布,与桶状结构的细分(即空心与壁;或IVa层与IVb层)没有可靠的关系。在研究的第二部分,我们证明含小白蛋白的神经元是桶状皮质IV层中丘脑传入纤维靶向的主要γ-氨基丁酸能细胞类型,因为所有研究的小白蛋白阳性细胞都接受了来自丘脑腹后内侧核的多个突触接触(每个神经元多达八个突触)。这些结果表明,负责躯体周围抑制的中间神经元(已知含有小白蛋白的篮状细胞和吊灯细胞)可能会被丘脑传入纤维强烈兴奋,尽管与主细胞的棘突相比,丘脑突触在γ-氨基丁酸能元件上的比例相对较低,并且参与皮质感觉信息处理的早期阶段。