Neural circuits in the mouse retina support color vision in the upper visual field

International audienceColor vision is essential for an animal's survival. It starts in the retina, where signals from different photoreceptor types are locally compared by neural circuits. Mice, like most mammals, are dichromatic with two cone types. They can discriminate colors only in their upper visual field. In the corresponding ventral retina, however, most cones display the same spectral preference, thereby presumably impairing spectral comparisons. In this study, we systematically investigated the retinal circuits underlying mouse color vision by recording light responses from cones, bipolar and ganglion cells. Surprisingly, most color-opponent cells are located in the ventral retina, with rod photoreceptors likely being involved. Here, the complexity of chromatic processing increases from cones towards the retinal output, where non-linear center-surround interactions create specific color-opponent output channels to the brain. This suggests that neural circuits in the mouse retina are tuned to extract color from the upper visual field, aiding robust detection of predators and ensuring the animal's survival

Data for Center-surround interactions underlie bipolar cell motion sensitivity in the mouse retina

Data from the publication "Center-surround interactions underlie bipolar cell motion sensitivity in the mouse retina" published in Nature Communications (2022) https://doi.org/10.1038/s41467-022-32762-7. Code for working with this dataset may be found at https://github.com/eulerlab/bc-motio

Center-surround interactions underlie bipolar cell motion sensitivity in the mouse retina

Motion sensing is a critical aspect of vision. We studied the representation of motion in mouse retinal bipolar cells and found that some bipolar cells are radially direction selective, preferring the origin of small object motion trajectories. Using a glutamate sensor, we directly observed bipolar cells synaptic output and found that there are radial direction selective and non-selective bipolar cell types, the majority being selective, and that radial direction selectivity relies on properties of the center-surround receptive field. We used these bipolar cell receptive fields along with connectomics to design biophysical models of downstream cells. The models and additional experiments demonstrated that bipolar cells pass radial direction selective excitation to starburst amacrine cells, which contributes to their directional tuning. As bipolar cells provide excitation to most amacrine and ganglion cells, their radial direction selectivity may contribute to motion processing throughout the visual system

Suppression without inhibition: how retinal computation contributes to saccadic suppression

Sequential light stimulation reduces the sensitivity of retinal ganglion cells via three different mechanisms which differentially affect ON and OFF cells