Bertolesi Gabriel E, Hehr Carrie L, McFarlane Sarah
Department of Cell Biology and Anatomy, Hotchkiss Brain Institute, University of Calgary, 3330 Hospital Dr, NW, Health Sciences Building, Room 2164, Calgary AB T2N4N1, Canada.
Neural Dev. 2014 Feb 13;9:3. doi: 10.1186/1749-8104-9-3.
Light information is sorted by neuronal circuits to generate image-forming (IF) (interpretation and tracking of visual objects and patterns) and non-image-forming (NIF) tasks. Among the NIF tasks, photic entrainment of circadian rhythms, the pupillary light reflex, and sleep are all associated with physiological responses, mediated mainly by a small group of melanopsin-expressing retinal ganglion cells (mRGCs). Using Xenopus laevis as a model system, and analyzing the c-fos expression induced by light as a surrogate marker of neural activity, we aimed to establish the developmental time at which the cells participating in both systems come on-line in the retina.
We found that the peripheral retina contains 80% of the two melanopsin-expressing cell types we identified in Xenopus: melanopsin-expressing horizontal cells (mHCs; opn4m+/opn4x+/Prox1+) and mRGCs (2.7% of the total RGCs; opn4m+/opn4x+/Pax6+/Isl1), in a ratio of 6:1. Only mRGCs induced c-fos expression in response to light. Dopaminergic (tyrosine hydroxylase-positive; TH+) amacrine cells (ACs) may be part of the melanopsin-mediated circuit, as shown by preferential c-fos induction by blue light. In the central retina, two cell types in the inner nuclear layer (INL) showed light-mediated induction of c-fos expression [(On-bipolar cells (Otx2+/Isl1+), and a sub-population of ACs (Pax6-/Isl1-)], as well as two RGC sub-populations (Isl1+/Pax6+ and Isl1+/Pax6-). Melanopsin and opsin expression turned on a day before the point at which c-fos expression could first be activated by light (Stage 37/38), in cells of both the classic vision circuit, and those that participate in the retinal component of the NIF circuit. Key to the classic vision circuit is that the component cells engage from the beginning as functional 'unit circuits' of two to three cells in the INL for every RGC, with subsequent growth of the vision circuit occurring by the wiring in of more units.
We identified melanopsin-expressing cells and specific cell types in the INL and the RGC layer which induce c-fos expression in response to light, and we determined the developmental time when they become active. We suggest an initial formulation of retinal circuits corresponding to the classic vision pathway and melanopsin-mediated circuits to which they may contribute.
光信息由神经回路进行分类,以产生成像(IF)(视觉对象和模式的解释与追踪)和非成像(NIF)任务。在NIF任务中,昼夜节律的光驱动、瞳孔对光反射和睡眠均与生理反应相关,这些反应主要由一小群表达黑视蛋白的视网膜神经节细胞(mRGCs)介导。我们以非洲爪蟾作为模型系统,并分析由光诱导的c-fos表达作为神经活动的替代标志物,旨在确定参与这两个系统的细胞在视网膜中开始发挥作用的发育时间。
我们发现,外周视网膜包含我们在非洲爪蟾中鉴定出的两种表达黑视蛋白细胞类型的80%:表达黑视蛋白的水平细胞(mHCs;opn4m+/opn4x+/Prox1+)和mRGCs(占总RGCs的2.7%;opn4m+/opn4x+/Pax6+/Isl1),比例为6:1。只有mRGCs对光产生反应诱导c-fos表达。多巴胺能(酪氨酸羟化酶阳性;TH+)无长突细胞(ACs)可能是黑视蛋白介导回路的一部分,蓝光优先诱导c-fos表达表明了这一点。在中央视网膜中,内核层(INL)的两种细胞类型显示出光介导的c-fos表达诱导[(开双极细胞(Otx2+/Isl1+)和ACs的一个亚群(Pax6-/Isl1-)],以及两个RGC亚群(Isl1+/Pax6+和Isl1+/Pax6-)。在经典视觉回路的细胞以及参与NIF回路视网膜成分的细胞中,黑视蛋白和视蛋白的表达在c-fos表达首次能被光激活之前一天开启(第37/38阶段)。经典视觉回路的关键在于,组成细胞从一开始就作为每个RGC在INL中由两到三个细胞组成的功能性“单位回路”发挥作用,随后视觉回路通过更多单位的连接而生长。
我们鉴定出了在INL和RGC层中表达黑视蛋白且对光产生反应诱导c-fos表达的细胞和特定细胞类型,并确定了它们开始活跃的发育时间。我们提出了与经典视觉通路以及它们可能参与的黑视蛋白介导回路相对应的视网膜回路的初步构想。