Cucchiaro J B, Uhlrich D J, Sherman S M
Department of Neurobiology, State University of New York, Stony Brook 11794-5230.
J Comp Neurol. 1993 Aug 22;334(4):618-30. doi: 10.1002/cne.903340409.
We have recently shown in cats that many neurons projecting to the lateral geniculate nucleus from the pretectum use gamma-amino butyric acid (GABA) as their neurotransmitter. We sought to determine the morphology of synaptic terminals and synapses formed by these pretectal axons and the extent to which they resemble other GABAergic terminals found in the geniculate neuropil (i.e., from geniculate interneurons and cells of the nearby perigeniculate nucleus). To do this, we labeled a population of pretectal axons with the anterograde tracer Phaseolus vulgaris leucoagglutinin and analyzed the morphology and synaptology of labeled pretectal terminals in the A-laminae of the cat's lateral geniculate nucleus. The pretectal projection, which arises primarily from the nucleus of the optic tract (NOT), provides synaptic innervation to elements in the geniculate neuropil. The labeled NOT terminals are densely packed with vesicles, contain dark mitochondria, and form symmetrical synaptic contacts. These are characteristics of the F1 type of terminal, and we know from other studies that GABAergic axon terminals from interneurons and perigeniculate cells also give rise to F1 terminals. We compared our population of NOT terminals with labeled perigeniculate and unlabeled F1 terminals selected from the geniculate neuropil and found that all three populations share many morphological characteristics. Both qualitative and quantitative assessments of the pretectal terminals suggest that these are a type of F1 terminal. Most pretectal terminals selectively form synapses onto geniculate profiles that contain irregularly distributed vesicles and dark mitochondria and that are postsynaptic to other types of terminals. These postsynaptic targets thus exhibit features of another class of inhibitory, GABAergic terminal known as F2 terminals, which are the specialized appendages of geniculate interneurons. Pretectal inputs, being GABAergic, may thus serve to inhibit local interneuronal outputs. Pretectal axons also innervate the perigeniculate nucleus, in which the only targets are the other main type of inhibitory, GABAergic neurons. These results suggest that the pretectum may facilitate retinal transmission through the lateral geniculate nucleus by providing inhibition to the local inhibitory cells: the interneurons and probably perigeniculate cells. This would serve to release geniculate relay cells from inhibition.
我们最近在猫身上发现,许多从前庭投射到外侧膝状体核的神经元使用γ-氨基丁酸(GABA)作为神经递质。我们试图确定这些前庭轴突形成的突触终末和突触的形态,以及它们与在膝状体神经毡中发现的其他GABA能终末(即来自膝状体中间神经元和附近的膝状体旁核细胞)的相似程度。为此,我们用顺行示踪剂菜豆白细胞凝集素标记了一群前庭轴突,并分析了猫外侧膝状体核A层中标记的前庭终末的形态和突触学。前庭投射主要起源于视束核(NOT),为膝状体神经毡中的神经元提供突触支配。标记的NOT终末充满了囊泡,含有深色线粒体,并形成对称的突触联系。这些是F1型终末的特征,我们从其他研究中知道,来自中间神经元和膝状体旁细胞的GABA能轴突终末也会产生F1终末。我们将我们的NOT终末群体与从膝状体神经毡中选择的标记的膝状体旁终末和未标记的F1终末进行了比较,发现这三个群体具有许多形态学特征。对前庭终末的定性和定量评估都表明,它们是一种F1终末。大多数前庭终末选择性地与含有不规则分布囊泡和深色线粒体的膝状体神经元形成突触,并且是其他类型终末的突触后神经元。这些突触后靶点因此表现出另一类抑制性GABA能终末(称为F2终末)的特征,F2终末是膝状体中间神经元的特化附属物。因此,作为GABA能的前庭输入可能起到抑制局部中间神经元输出的作用。前庭轴突也支配膝状体旁核,其中唯一的靶点是另一种主要类型的抑制性GABA能神经元。这些结果表明,前庭可能通过对局部抑制性细胞(中间神经元以及可能的膝状体旁细胞)的抑制作用来促进视网膜通过外侧膝状体核的传递。这将有助于使膝状体中继细胞从抑制中释放出来。