Dávid Csaba, Schleicher Axel, Zuschratter Werner, Staiger Jochen F
Albert-Ludwigs-University Freiburg, Institute of Anatomy and Cell Biology, Department of Neuroanatomy, D-79001 Freiburg, Germany.
Eur J Neurosci. 2007 Apr;25(8):2329-40. doi: 10.1111/j.1460-9568.2007.05496.x.
gamma-Aminobutyric acid (GABA)ergic interneurons of neocortex consist of many subgroups with extremely heterogeneous morphological, physiological and molecular properties. To explore the putative effect of the vasoactive intestinal polypeptide-immunopositive (VIP +) neurons on neocortical circuitry, the number and distribution of VIP + boutons were analysed on somatodendritic domains of 272 parvalbumin immunopositive (PV +) 3D-reconstructed neurons. The synaptic nature of 91% of somatic and 76% of dendritic contacts was verified by electron microscopy. The target PV + neurons were separated in two significantly different groups by means of cluster analysis. The first group (Cluster 1, 26%) received on average five times more VIP + synapses than those of the second group. The second group (Cluster 2, 74%) contained cells that were poorly innervated by VIP + boutons or did not have either somatic or dendritic or any VIP innervation at all. The cells of Cluster 1 had a soma size and total dendritic length significantly smaller than that of Cluster 2, however, they received three times more dendritic synapses, which resulted in a five times higher VIP + synaptic density on dendrites. Our results showed that although most of the PV + cells are innervated by VIP + boutons at a varying degree, some 6% of PV + cells received no input from VIP + interneurons. This suggests a refined morphological basis to influence the majority of the PV + interneurons, which are very effectively controlling pyramidal cell firing. Together with metabolic and neuromodulatory effects of VIP, this would probably result in an enhanced responsiveness of the latter cell type to tactile stimuli.
新皮层的γ-氨基丁酸(GABA)能中间神经元由许多亚组组成,它们在形态、生理和分子特性上具有极大的异质性。为了探究血管活性肠肽免疫阳性(VIP+)神经元对新皮层神经回路的假定作用,我们分析了272个小白蛋白免疫阳性(PV+)的三维重建神经元的体树突域上VIP+终扣的数量和分布。通过电子显微镜证实了91%的体细胞接触和76%的树突接触的突触性质。通过聚类分析将目标PV+神经元分为两个显著不同的组。第一组(聚类1,26%)平均接受的VIP+突触比第二组多五倍。第二组(聚类2,74%)包含的细胞受VIP+终扣支配较少,或者根本没有体细胞、树突或任何VIP支配。聚类1的细胞的胞体大小和总树突长度明显小于聚类2,但它们接受的树突突触多三倍,这导致树突上的VIP+突触密度高五倍。我们的结果表明,虽然大多数PV+细胞在不同程度上受VIP+终扣支配,但约6%的PV+细胞没有从VIP+中间神经元接受输入。这表明存在一种精细的形态学基础来影响大多数PV+中间神经元,它们能非常有效地控制锥体细胞的放电。连同VIP的代谢和神经调节作用,这可能会导致后一种细胞类型对触觉刺激的反应性增强。