
AbstractVisual features extracted by retinal circuits are streamed into higher visual areas (HVAs) after being processed along the visual hierarchy. However, how specialized neuronal representations of HVAs are built, based on retinal output channels, remained unclear. Here, we addressed this question by determining the effects of genetically disrupting retinal direction selectivity on motion-evoked responses in visual stages from the retina to HVAs in mice. Direction-selective (DS) cells in the rostrolateral (RL) area that prefer higher temporal frequencies, and that change direction tuning bias as the temporal frequency of a stimulus increases, are selectively reduced upon retinal manipulation. DS cells in the primary visual cortex projecting to area RL, but not to the posteromedial area, were similarly affected. Therefore, the specific connectivity of cortico-cortical projection neurons routes feedforward signaling originating from retinal DS cells preferentially to area RL. We thus identify a cortical processing stream for motion computed in the retina.
Male, MOTION, Science, Motion Perception, MOUSE, Article, Retina, Mice, FUNCTIONAL SPECIALIZATION, Orientation, MAPS, REVEALS, Animals, Visual Pathways, Visual Cortex, Neurons, Q, CIRCUIT, RESPONSE PROPERTIES, GANGLION-CELLS, Mice, Inbred C57BL, PRIMARY VISUAL-CORTEX, Cytoskeletal Proteins, Female, LATERAL GENICULATE-NUCLEUS, Photic Stimulation
Male, MOTION, Science, Motion Perception, MOUSE, Article, Retina, Mice, FUNCTIONAL SPECIALIZATION, Orientation, MAPS, REVEALS, Animals, Visual Pathways, Visual Cortex, Neurons, Q, CIRCUIT, RESPONSE PROPERTIES, GANGLION-CELLS, Mice, Inbred C57BL, PRIMARY VISUAL-CORTEX, Cytoskeletal Proteins, Female, LATERAL GENICULATE-NUCLEUS, Photic Stimulation
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