Hurd L B, Eldred W D
Department of Anatomy and Neurobiology, Boston University School of Medicine, MA 02215.
Vis Neurosci. 1993 May-Jun;10(3):455-71. doi: 10.1017/s0952523800004685.
Although serotonin is thought to be a neurotransmitter in a number of retinal systems, much of the precise synaptic connectivity of serotonergic neurons is unknown. To address this issue, we used an antiserum directed against serotonin to label serotonergic bipolar and amacrine cells in the turtle retina. Light-microscopic analysis of labeled amacrine and bipolar cells indicated that both had bistratified dendritic arborizations primarily in stratum 1 and in strata 4/5 of the inner plexiform layer. Ultrastructural analysis of the neurocircuitry of these cells indicated that the processes of labeled bipolar cells in the outer plexiform layer made basal junction contacts with photoreceptor terminals. Only in rare instances did labeled bipolar cells processes invaginate near photoreceptor ribbon synapses. Processes of labeled bipolar cells received both conventional and small ribbon synaptic contacts in the outer plexiform layer. Bipolar cell processes in stratum 1 of the inner plexiform layer synapsed onto either amacrine/amacrine or amacrine/ganglion cell dyads, and made rare ribbon synaptic contacts onto labeled amacrine cell processes. Synaptic inputs to serotonergic bipolar cells in stratum 1 were from unlabeled bipolar and amacrine cells. Bipolar cell contacts in strata 4/5 were similar to those in stratum 1, but were fewer in number and no bipolar cell inputs were seen. Labeled amacrine cell output in both strata was onto other unlabeled amacrine cells and ganglion cells; but synaptic outputs to unlabeled bipolar cells were only seen in strata 4/5. In both strata 1 and 4/5, synaptic inputs to labeled amacrine cells were from both unlabeled amacrine cells and labeled bipolar cells. The serotonergic amacrine cells had many more synaptic interactions in stratum 1 than in strata 4/5 which supports the role of serotonergic bipolar cells in the OFF pathway of retinal processing. Interactions between serotonergic bipolar and amacrine cells may play an important role in visual processing.
尽管血清素被认为是许多视网膜系统中的一种神经递质,但血清素能神经元的许多精确突触连接尚不清楚。为了解决这个问题,我们使用了一种针对血清素的抗血清来标记乌龟视网膜中的血清素能双极细胞和无长突细胞。对标记的无长突细胞和双极细胞的光学显微镜分析表明,两者都有双分层树突分支,主要位于内网状层的第1层和第4/5层。对这些细胞神经回路的超微结构分析表明,外网状层中标记的双极细胞的突起与光感受器终末形成基底连接接触。只有在极少数情况下,标记的双极细胞突起会在内陷光感受器带状突触附近内陷。标记的双极细胞突起在外网状层接受常规和小带状突触接触。内网状层第1层的双极细胞突起与无长突细胞/无长突细胞或无长突细胞/神经节细胞二元组形成突触,并在标记的无长突细胞突起上形成罕见的带状突触接触。第1层血清素能双极细胞的突触输入来自未标记的双极细胞和无长突细胞。第4/5层的双极细胞接触与第1层相似,但数量较少,未见双极细胞输入。两层中标记的无长突细胞输出均作用于其他未标记的无长突细胞和神经节细胞;但对未标记双极细胞的突触输出仅在第4/5层可见。在第1层和第4/5层中,标记的无长突细胞的突触输入均来自未标记的无长突细胞和标记的双极细胞。血清素能无长突细胞在第1层的突触相互作用比在第4/5层多,这支持了血清素能双极细胞在视网膜处理OFF通路中的作用。血清素能双极细胞和无长突细胞之间的相互作用可能在视觉处理中起重要作用。