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海洋硬骨鱼线纹尖塘鳢视网膜中移位的小无长突细胞

Displaced small amacrine cells in the retina of the marine teleost Callionymus lyra L.

作者信息

van Haesendonck E, Missotten L

机构信息

Eye Research Laboratory, Universitair Ziekenhuis St. Rafaël, Leuven, Belgium.

出版信息

Vision Res. 1987;27(9):1431-43. doi: 10.1016/0042-6989(87)90153-2.

Abstract

The displaced small amacrine cells (DSA cells) in the dorsal pure cone part of the retina of the marine teleost Callionymus lyra have been analysed in a combined light and electron microcopical study. These unistratified cells have their dendritic arborization at 70% of the depth of the inner plexiform layer (P5 level). The DSA cells constitute a dense population and have variable dendritic field sizes. The bipolar input occurs in the P5,1 and the P5,2 pattern layer. The short, central DSA dendrites make ribbon synapses with midget mixed di-cone bipolar cells and with two types of pure cone bipolar cells. The amacrine input and output occurs in the fibrous layer that separates both pattern layers. The dendritic arborization is most extensive and the dendrites of neighbouring DSA cells are interconnected. The thick, central DSA dendrites are presynaptic to adjacent DSA cells and possibly to large bistratified and diffuse ganglion cells. The fine, peripheral DSA dendrites receive input from neighbouring DSA cells and probably from large uni- and bistratified and diffuse amacrine cells. A matching population of regularly placed small amacrine cells (RSA cells) has been observed. Their unistratified dendritic arborization is situated at 20% of the depth of the inner plexiform layer. The synaptic relations of RSA cells have not yet been completely analysed in detail. However, results up till now indicate that they most probably receive input from two bipolar cell types, one of which may be a pure cone type. In addition, the large bistratified amacrine and ganglion cells may be synaptically connected to the RSA cells as well as to the DSA cells.

摘要

在一项光镜与电镜联合研究中,对海生硬骨鱼线纹眶棘鲈视网膜背侧纯视锥部分的移位小无长突细胞(DSA细胞)进行了分析。这些单层细胞的树突分支位于内网状层深度的70%处(P5水平)。DSA细胞构成密集群体,树突野大小各异。双极输入出现在P5,1和P5,2模式层。短小的中央DSA树突与侏儒混合双视锥双极细胞以及两种纯视锥双极细胞形成带状突触。无长突细胞的输入和输出发生在分隔两个模式层的纤维层。树突分支最为广泛,相邻DSA细胞的树突相互连接。粗大的中央DSA树突对相邻DSA细胞以及可能对大型双分层和弥散型神经节细胞是突触前的。纤细的外周DSA树突接收来自相邻DSA细胞以及可能来自大型单分层、双分层和弥散型无长突细胞的输入。已观察到一群位置规则的小无长突细胞(RSA细胞)。它们的单层树突分支位于内网状层深度的20%处。RSA细胞的突触关系尚未完全详细分析。然而,到目前为止的结果表明,它们很可能接收来自两种双极细胞类型的输入,其中一种可能是纯视锥类型。此外,大型双分层无长突细胞和神经节细胞可能与RSA细胞以及DSA细胞形成突触连接。

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