Cauli B, Porter J T, Tsuzuki K, Lambolez B, Rossier J, Quenet B, Audinat E
Neurobiologie et Diversité Cellulaire, Centre Nationale de la Recherche Scientifique, Unité Mixte de Recherche 7637, Centre Nationale de la Recherche Scientifique, ecole Supérieure de Physique et Chimie Industrielles, Paris, France.
Proc Natl Acad Sci U S A. 2000 May 23;97(11):6144-9. doi: 10.1073/pnas.97.11.6144.
A classification of fusiform neocortical interneurons (n = 60) was performed with an unsupervised cluster analysis based on the comparison of multiple electrophysiological and molecular parameters studied by patch-clamp and single-cell multiplex reverse transcription-PCR in rat neocortical acute slices. The multiplex reverse transcription-PCR protocol was designed to detect simultaneously the expression of GAD65, GAD67, calbindin, parvalbumin, calretinin, neuropeptide Y, vasoactive intestinal peptide (VIP), somatostatin (SS), cholecystokinin, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid, kainate, N-methyl-d-aspartate, and metabotropic glutamate receptor subtypes. Three groups of fusiform interneurons with distinctive features were disclosed by the cluster analysis. The first type of fusiform neuron (n = 12), termed regular spiking nonpyramidal (RSNP)-SS cluster, was characterized by a firing pattern of RSNP cells and by a high occurrence of SS. The second type of fusiform neuron (n = 32), termed RSNP-VIP cluster, predominantly expressed VIP and also showed firing properties of RSNP neurons with accommodation profiles different from those of RSNP-SS cells. Finally, the last type of fusiform neuron (n = 16) contained a majority of irregular spiking-VIPergic neurons. In addition, the analysis of glutamate receptors revealed cell-type-specific expression profiles. This study shows that combinations of multiple independent criteria define distinct neocortical populations of interneurons potentially involved in specific functions.
基于对大鼠新皮质急性脑片中通过膜片钳和单细胞多重逆转录聚合酶链反应研究的多个电生理和分子参数的比较,采用无监督聚类分析对60个梭形新皮质中间神经元进行了分类。多重逆转录聚合酶链反应方案旨在同时检测谷氨酸脱羧酶65(GAD65)、谷氨酸脱羧酶67(GAD67)、钙结合蛋白、小白蛋白、钙视网膜蛋白、神经肽Y、血管活性肠肽(VIP)、生长抑素(SS)、胆囊收缩素、α-氨基-3-羟基-5-甲基-4-异恶唑丙酸、海人藻酸、N-甲基-D-天冬氨酸和代谢型谷氨酸受体亚型的表达。聚类分析揭示了具有独特特征的三组梭形中间神经元。第一种类型的梭形神经元(n = 12),称为规则放电非锥体(RSNP)-SS簇,其特征是具有RSNP细胞的放电模式且SS的出现频率较高。第二种类型的梭形神经元(n = 32),称为RSNP-VIP簇,主要表达VIP,并且还表现出RSNP神经元的放电特性,其适应模式与RSNP-SS细胞不同。最后,最后一种类型的梭形神经元(n = 16)包含大多数不规则放电的VIP能神经元。此外,对谷氨酸受体的分析揭示了细胞类型特异性的表达谱。这项研究表明,多个独立标准的组合定义了可能参与特定功能的不同新皮质中间神经元群体。