Ohara P T, Lieberman A R
Department of Anatomy, University of California at San Francisco 94194-0452.
J Neurocytol. 1993 Sep;22(9):815-25. doi: 10.1007/BF01181326.
We describe here, and review, the ultrastructural features and synaptic relationships of flat-vesicle containing, presumptively inhibitory presynaptic elements in the glomerular and extraglomerular neuropils of the thalamic ventrobasal (VB) nucleus in monkey, cat and rat. This account is based on EM study of normal material, LM and EM immunocytochemistry for GABA, anterograde tracing with HRP and EM of physiologically characterized interneurons intracellularly injected with HRP. It emerges clearly from this study that attempts to categorize flat-vesicle containing terminals in thalamic tissue as either F-boutons (axon terminals with flattened synaptic vesicles and Gray type II synaptic specializations) or P-boutons (dendritic appendages of interneurons with flattened vesicles) by examining only single sections are likely to produce unreliable results. In many cases it is only by studying serial sections that such profiles can be unambiguously identified. Within glomeruli the P-boutons participate in triplet (triadic) synapses which are thought to mediate rapid feed forward inhibition of projection cells, and serial synaptic arrays involving other P-boutons. Since P-boutons from more than one interneuron are present in individual VB glomeruli, P-bouton to P-bouton synapses may mediate disinhibition of interneurons. We show that dendritic shafts of interneurons make and receive synaptic contacts and that in the monkey, at least, reciprocal synaptic contacts between shafts or between a shaft and a P-bouton are not uncommon. Finally, we confirm that in the rat VB there are insignificant numbers of P-boutons or cells with the morphological and transmitter characteristics of interneurons and we suggest that comparative electrophysiological studies of inhibitory events in rat VB versus those in cat or monkey VB during transmission of somatosensory information might help to clarify the roles of thalamic intrinsic neurons.
我们在此描述并回顾了猴、猫和大鼠丘脑腹侧基底(VB)核的肾小球和球外神经毡中含有扁平囊泡的、推测为抑制性突触前元件的超微结构特征和突触关系。本报告基于对正常材料的电镜研究、GABA的光镜和电镜免疫细胞化学、用HRP进行的顺行追踪以及对经细胞内注射HRP的生理特征性中间神经元的电镜观察。从这项研究中可以清楚地看出,仅通过检查单个切片就试图将丘脑组织中含有扁平囊泡的终末分类为F型终扣(具有扁平突触囊泡和Gray II型突触特化的轴突终末)或P型终扣(具有扁平囊泡的中间神经元的树突附属物)很可能会产生不可靠的结果。在许多情况下,只有通过研究连续切片才能明确识别这些结构。在肾小球内,P型终扣参与三联体(三元)突触,这些突触被认为介导投射细胞的快速前馈抑制,以及涉及其他P型终扣的连续突触阵列。由于单个VB肾小球中存在来自多个中间神经元的P型终扣,P型终扣到P型终扣的突触可能介导中间神经元的去抑制。我们发现中间神经元的树突干形成并接受突触联系,并且至少在猴子中,树突干之间或树突干与P型终扣之间的相互突触联系并不罕见。最后,我们证实,在大鼠VB中,具有中间神经元形态和递质特征的P型终扣或细胞数量极少,我们建议对大鼠VB与猫或猴子VB在体感信息传递过程中抑制性事件进行比较电生理研究,可能有助于阐明丘脑内在神经元的作用。