Yang C Y, Yazulla S
Department of Neurobiology and Behavior, State University of New York, Stony Brook 11794.
J Comp Neurol. 1988 Jun 15;272(3):343-57. doi: 10.1002/cne.902720305.
Putative glycinergic neurons in the larval tiger salamander retina were localized by a comparative analysis of high affinity 3H-glycine uptake and glycine-like immunoreactivity (Gly-IR) at the light microscopic level. Commonly labeled neurons include at least three types of amacrine cell (Type IAd, Type IAb, Type IIAd; distinguished by soma location and dendritic ramification), cell bodies in the ganglion cell layer (GCL), and rarely observed Type II (inner) bipolar cells. With the increased resolution provided by Gly-IR, we identified a Type IAa amacrine cell, two types of Type IIAd amacrine cells, and Gly-IR interplexiform cells. Gly-IR axons in longitudinal sections of the optic nerve indicate the presence of Gly-IR ganglion cells. The percentage of labeled somas in the inner nuclear layer (INL) compared to all cells in each layer was similar for the two methods: 30-40% in INL 2 (middle layer of somas), 30-40% in INL 3 (inner layer of somas), and about 5% in the GCL. Labeled processes were found throughout the full thickness of the inner plexiform layer (IPL), but with a much denser band in the proximal half (sublamina b). The only major difference between the two methods (3H-glycine uptake vs. Gly-IR) was that Type I (outer) bipolar cells were labeled only by 3H-glycine uptake; these cells were more lightly labeled with silver grains than cell bodies in either INL 2 or INL 3. Postembed labeling of 1 micron Durcupan plastic sections for Gly-IR showed the same pattern, but with much higher resolution, as obtained with 10 micron cryostat sections. This study indicates extensive colocalization of labeling by both probes in INL 2, INL 3, the IPL, and the GCL. We conclude that Gly-IR can serve as a valid and reliable marker for glycine-containing neurons in this retina and suggest that glycine serves as a transmitter for several morphologically distinct types of amacrine cell, an interplexiform cell, and perhaps a small percentage of Type II bipolar cells and ganglion cells.
通过在光学显微镜水平上对高亲和力³H-甘氨酸摄取和甘氨酸样免疫反应性(Gly-IR)进行比较分析,定位了虎螈幼体视网膜中假定的甘氨酸能神经元。共同标记的神经元至少包括三种无长突细胞(IAd型、IAb型、IIAd型;根据胞体位置和树突分支区分)、神经节细胞层(GCL)中的胞体,以及很少观察到的II型(内侧)双极细胞。随着Gly-IR提供的分辨率提高,我们鉴定出了IAa型无长突细胞、两种IIAd型无长突细胞以及Gly-IR网间细胞。视神经纵切面上的Gly-IR轴突表明存在Gly-IR神经节细胞。两种方法中,内核层(INL)中标记胞体占各层所有细胞的百分比相似:INL 2(胞体中层)为30 - 40%,INL 3(胞体内层)为30 - 40%,GCL中约为5%。在内网状层(IPL)全层均发现了标记的突起,但近端一半(b亚层)的带更密集。两种方法(³H-甘氨酸摄取与Gly-IR)之间唯一的主要差异在于,I型(外侧)双极细胞仅通过³H-甘氨酸摄取被标记;这些细胞被银颗粒标记的程度比INL 2或INL 3中的胞体更浅。对1微米Durcupan塑料切片进行Gly-IR的包埋后标记显示出与10微米低温恒温器切片相同的模式,但分辨率更高。本研究表明,两种探针在INL 2、INL 3、IPL和GCL中的标记广泛共定位。我们得出结论,Gly-IR可作为该视网膜中含甘氨酸神经元的有效且可靠标记,并表明甘氨酸作为几种形态学上不同类型的无长突细胞、一种网间细胞以及可能一小部分II型双极细胞和神经节细胞的神经递质。