Departments of Neurobiology.
Neurosensorics.
J Neurosci. 2018 Feb 21;38(8):2015-2028. doi: 10.1523/JNEUROSCI.0141-17.2018. Epub 2018 Jan 19.
In the mammalian retina, horizontal cells receive glutamatergic inputs from many rod and cone photoreceptors and return feedback signals to them, thereby changing photoreceptor glutamate release in a light-dependent manner. Horizontal cells also provide feedforward signals to bipolar cells. It is unclear, however, how horizontal cell signals also affect the temporal, spatial, and contrast tuning in retinal output neurons, the ganglion cells. To study this, we generated a genetically modified mouse line in which we eliminated the light dependency of feedback by deleting glutamate receptors from mouse horizontal cells. This genetic modification allowed us to investigate the impact of horizontal cells on ganglion cell signaling independent of the actual mode of feedback in the outer retina and without pharmacological manipulation of signal transmission. In control and genetically modified mice (both sexes), we recorded the light responses of transient OFF-α retinal ganglion cells in the intact retina. Excitatory postsynaptic currents (EPSCs) were reduced and the cells were tuned to lower temporal frequencies and higher contrasts, presumably because photoreceptor output was attenuated. Moreover, receptive fields of recorded cells showed a significantly altered surround structure. Our data thus suggest that horizontal cells are responsible for adjusting the dynamic range of retinal ganglion cells and, together with amacrine cells, contribute to the center/surround organization of ganglion cell receptive fields in the mouse. Horizontal cells represent a major neuronal class in the mammalian retina and provide lateral feedback and feedforward signals to photoreceptors and bipolar cells, respectively. The mode of signal transmission remains controversial and, moreover, the contribution of horizontal cells to visual processing is still elusive. To address the question of how horizontal cells affect retinal output signals, we recorded the light responses of transient OFF-α retinal ganglion cells in a newly generated mouse line. In this mouse line, horizontal cell signals were no longer modulated by light. With light response recordings, we show that horizontal cells increase the dynamic range of retinal ganglion cells for contrast and temporal changes and contribute to the center/surround organization of their receptive fields.
在哺乳动物的视网膜中,水平细胞从许多视杆和视锥感光细胞接收谷氨酸能输入,并向它们返回反馈信号,从而以光依赖的方式改变感光细胞谷氨酸的释放。水平细胞还向双极细胞提供前馈信号。然而,目前尚不清楚水平细胞信号如何也影响视网膜输出神经元(神经节细胞)的时间、空间和对比度调谐。为了研究这一点,我们生成了一种基因修饰的小鼠品系,其中通过从小鼠水平细胞中删除谷氨酸受体,消除了反馈的光依赖性。这种基因修饰使我们能够在不依赖于外视网膜中反馈的实际模式且无需对信号传输进行药理学处理的情况下,研究水平细胞对神经节细胞信号的影响。在对照和基因修饰的小鼠(雌雄皆有)中,我们在完整的视网膜中记录了瞬态 OFF-α 视网膜神经节细胞的光反应。兴奋性突触后电流(EPSC)减少,细胞调谐至更低的时间频率和更高的对比度,这可能是因为光感受器的输出被减弱。此外,记录细胞的感受野显示出明显改变的环绕结构。因此,我们的数据表明水平细胞负责调节视网膜神经节细胞的动态范围,并且与无长突细胞一起,有助于在小鼠中形成神经节细胞感受野的中心/环绕结构。水平细胞是哺乳动物视网膜中的主要神经元类群,分别向光感受器和双极细胞提供侧向反馈和前馈信号。信号传输的模式仍然存在争议,而且水平细胞对视觉处理的贡献仍然难以捉摸。为了解决水平细胞如何影响视网膜输出信号的问题,我们在一个新生成的小鼠品系中记录了瞬态 OFF-α 视网膜神经节细胞的光反应。在这个小鼠品系中,水平细胞信号不再受光调制。通过光反应记录,我们表明水平细胞增加了视网膜神经节细胞对对比度和时间变化的动态范围,并有助于它们感受野的中心/环绕组织。