Haverkamp S, Eldred W D, Ottersen O P, Pow D, Ammermüller J
Department of Biology, University of Oldenburg, Germany.
J Comp Neurol. 1997 Dec 15;389(2):235-48. doi: 10.1002/(sici)1096-9861(19971215)389:2<235::aid-cne4>3.0.co;2-2.
Previous studies have proposed models of the specific synaptic circuitry responsible for color processing in the turtle retina. To determine the accuracy of these models of the circuits underlying color opponency in the inner retina of the turtle (Pseudemys scripta), we have studied the physiology, morphology, and synaptic connectivity of identified amacrine and ganglion cells. These cells were first characterized electrophysiologically and were then stained with horseradish peroxidase. Postembedding electron immunocytochemistry for gamma-aminobutyric acid (GABA) and glycine was used to reveal the neurochemical identity of their synaptic inputs. The red-ON/green, blue-OFF small-field ganglion cell, classified as G24, branched primarily in strata S1, S4, and S5 of the inner plexiform layer (IPL). Ganglion cell G24 showed a complex receptive field organized into a red-ON center surrounded by an inhibitory region, which, in turn, was surrounded by a second excitatory region. Only the center responses were color opponent. The red-OFF/green, blue-ON large-field, stellate amacrine cell, classified as A23b, stratified exclusively in stratum S2, near the S2/S3 border. The color-coded center was surrounded by a luminosity, red-sensitive surround. Synaptic input to G24 and A23b was dominated by amacrine cells (89% and 87%, respectively). G24 received significant input from amacrine cell profiles with GABA (13% of total) as well as glycine (11% of total) immunoreactivity, mostly in the proximal stratum S5 of the IPL (64% and 67% of the total GABA- and glycine-immunoreactive input, respectively). Bipolar cell synaptic input was also found predominantly in S4 and S5 (89%). In contrast, we found no glycine-immunoreactive input to A23b, and the density of the GABA-immunoreactive amacrine cell synaptic input revealed a central (15%) to peripheral (3%) gradient within the dendritic tree. The results of the present study support the previous models of the synaptic circuitry responsible for color-opponent signal processing in the inner retina of the turtle.
以往的研究提出了负责海龟视网膜颜色处理的特定突触回路模型。为了确定这些海龟(伪彩龟)内视网膜中颜色拮抗回路模型的准确性,我们研究了已识别的无长突细胞和神经节细胞的生理学、形态学和突触连接性。这些细胞首先通过电生理学进行表征,然后用辣根过氧化物酶进行染色。采用针对γ-氨基丁酸(GABA)和甘氨酸的包埋后电子免疫细胞化学方法来揭示其突触输入的神经化学特性。红色开启/绿色、蓝色关闭的小视野神经节细胞,分类为G24,主要在内网状层(IPL)的S1、S4和S5层分支。神经节细胞G24显示出一个复杂的感受野,由一个红色开启的中心区域被一个抑制区域包围,而这个抑制区域又被第二个兴奋区域包围。只有中心反应是颜色拮抗的。红色关闭/绿色、蓝色开启的大视野、星状无长突细胞,分类为A23b,仅分层在靠近S2/S3边界的S2层。颜色编码的中心区域被一个亮度敏感、对红色敏感的周边区域包围。G24和A23b的突触输入主要由无长突细胞主导(分别为89%和87%)。G24从具有GABA免疫反应性(占总数的13%)以及甘氨酸免疫反应性(占总数的11%)的无长突细胞轮廓接收大量输入,主要在IPL的近端S5层(分别占GABA和甘氨酸免疫反应性输入总数的64%和67%)。双极细胞突触输入也主要在S4和S5层发现(89%)。相比之下,我们没有发现对A23b的甘氨酸免疫反应性输入,并且GABA免疫反应性无长突细胞突触输入的密度在树突状树中显示出从中心(15%)到周边(3%)的梯度。本研究结果支持了以往关于海龟内视网膜中负责颜色拮抗信号处理的突触回路模型。