Repérant Jacques, Ward Roger, Médina Monique, Kenigfest Natalia B, Rio Jean-Paul, Miceli Dom, Jay Bruno
Département Régulations, Développement et Diversité Moléculaire, USM 501, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Paris, France.
Brain Struct Funct. 2009 Sep;213(4-5):395-422. doi: 10.1007/s00429-009-0205-9. Epub 2009 Feb 28.
The ultrastructure of the retinorecipient layers of the lamprey optic tectum was analysed using tract tracing techniques combined with GABA and glutamate immunocytochemistry. Two types of neurons were identified; a population of large GABA-immunonegative cells, and a population of smaller, highly GABA-immunoreactive interneurons, some of whose dendrites contain synaptic vesicles (DCSV). Five types of axon terminals were identified and divided into two major categories. The first of these are GABA-immunonegative, highly glutamate-immunoreactive, contain round synaptic vesicles, make asymmetrical synaptic contacts, and can in turn be divided into AT1 and AT2 terminals. The AT1 terminals are those of the retinotectal projection. The origin of the nonretinal AT2 terminals could not be determined. AT1 and AT2 terminals establish synaptic contacts with DCSV, with dendrites of the retinopetal neurons (DRN), and with conventional dendritic (D) profiles. The terminals of the second category are GABA-immunoreactive and can similarly be divided into AT3 and AT4 terminals. The AT3 terminals contain pleiomorphic synaptic vesicles and make symmetrical synaptic contacts for the most part with glutamate-immunoreactive D profiles. The AT4 terminals contain rounded synaptic vesicles and make asymmetrical synaptic contacts with DRN, with DCSV, and with D profiles. A fifth, rarely observed category of terminals (AT5) contain both clear synaptic vesicles and a large number of dense-core vesicles. Synaptic triads involving AT1, AT2 or AT4 terminals are rare. Our findings are compared to these of previous studies of the fine structure and immunochemical properties of the retinorecipient layers of the optic tectum or superior colliculus of Gnathostomes.
运用示踪技术结合GABA和谷氨酸免疫细胞化学方法,对七鳃鳗视顶盖视网膜接收层的超微结构进行了分析。鉴定出两种类型的神经元:一群大型GABA免疫阴性细胞,以及一群较小的、高度GABA免疫反应性的中间神经元,其中一些中间神经元的树突含有突触小泡(DCSV)。鉴定出五种类型的轴突终末,并将其分为两大类。第一类是GABA免疫阴性、高度谷氨酸免疫反应性的,含有圆形突触小泡,形成不对称突触联系,进而可分为AT1和AT2终末。AT1终末是视网膜顶盖投射的终末。非视网膜AT2终末的起源无法确定。AT1和AT2终末与DCSV、视网膜向心性神经元(DRN)的树突以及常规树突(D)形态建立突触联系。第二类终末是GABA免疫反应性的,同样可分为AT3和AT4终末。AT3终末含有多形性突触小泡,大部分与谷氨酸免疫反应性的D形态形成对称突触联系。AT4终末含有圆形突触小泡,与DRN、DCSV以及D形态形成不对称突触联系。第五类终末(AT5)很少观察到,含有清亮突触小泡和大量致密核心小泡。涉及AT1、AT2或AT4终末的突触三联体很少见。我们的研究结果与之前对有颌类动物视顶盖或上丘视网膜接收层的精细结构和免疫化学特性的研究结果进行了比较。