scholarly journals Neurons in the mouse deep superior colliculus encode orientation/direction through suppression and extract selective visual features

2016 ◽  
Author(s):  
Shinya Ito ◽  
David A. Feldheim ◽  
Alan M. Litke

AbstractThe superior colliculus (SC) is an integrative sensorimotor structure that contributes to multiple visiondependent behaviors. It is a laminated structure; the superficial SC layers (sSC) contain cells that respond to visual stimuli, while the deep SC layers (dSC) contain cells that also respond to auditory and somatosensory stimuli. Despite the increasing interest in mice for visual system study, the differences in the visual response properties between the sSC and the dSC are largely unknown. Here we used a large-scale silicon probe recording system to examine the visual response properties of neurons within the SC of head-fixed, awake and behaving mice. We find that both the sSC and dSC cells respond to visual stimuli, but dSC cells have three key differences. (1) The majority of the dSC orientation/direction selective (OS/DS) cells have their firing rate suppressed by drifting sinusoidal gratings (negative OS/DS cells) rather than being stimulated like the sSC cells (positive OS/DS cells). (2) Almost all the dSC cells have complex-cell-like spatial summation nonlinearity, and a significantly smaller fraction of the positive OS/DS cells in the dSC respond to flashing spots than those in the sSC. (3) The dSC cells lack Y-like spatial summation nonlinearity unlike the sSC cells. These results provide the first description of cells that are suppressed by a visual stimulus with a specific orientation or direction, show that neurons in the dSC have properties analogous to cortical complex cells, and show the presence of Y-like nonlinearity in the sSC but their absence in the dSC.Significance statementThe superior colliculus receives visual input from the retina in its superficial layers (sSC) and induces eye/head orientating movements and innate defensive responses in its deeper layers (dSC). Despite their importance, very little is known about the visual response properties of dSC neurons. Using highdensity electrode recordings and novel model-based analysis, we find that the dSC contains cells with a novel property; they are suppressed by the orientation or direction of specific stimuli. We also show that dSC cells have properties similar to cortical “complex” cells. Conversely, cells with Y-like nonlinear spatial summation properties are located only in the sSC. These findings contribute to our understanding of how the SC processes visual inputs, a critical step in comprehending visually-guided behaviors.AcknowledgementsThis work was supported by the Brain Research Seed Funding provided by UCSC and from the National Institutes of Health Grant NEI R21EYO26758 to D. A. F. and A. M. L. We thank Michael Stryker for training on the electrophysiology experiments and his very helpful comments on the manuscript, Sotiris Masmanidis for providing us with the silicon probes, Forest Martinez-McKinney and Serguei Kachiguin for their technical contributions to the silicon probe system, Jeremiah Tsyporin for taking an image of neural tissues and the training of mice, Jena Yamada, Anahit Hovhannisyan, Corinne Beier, and Sydney Weiser, for their helpful comments on the manuscript.

1997 ◽  
Vol 78 (5) ◽  
pp. 2732-2741 ◽  
Author(s):  
M. T. Wallace ◽  
J. G. McHaffie ◽  
B. E. Stein

Wallace M. T., J. G. McHaffie, and B. E. Stein. Visual response properties and visuotopic representation in the newborn monkey superior colliculus. J. Neurophysiol. 78: 2732–2741, 1997. Visually responsive neurons were recorded in the superior colliculus (SC) of the newborn rhesus monkey. The receptive fields of these neurons were larger than those in the adult, but already were organized into a well-ordered map of visual space that was very much like that seen in mature animals. This included a marked expansion of the representation of the central 10° of the visual field and a systematic foveal to peripheral increase in receptive field size. Although newborn SC neurons had longer response latencies than did their adult counterparts, they responded vigorously to visual stimuli and exhibited many visual response properties that are characteristic of the adult. These included surround inhibition, within-field spatial summation, within-field spatial inhibition, binocularity, and an adult-like ocular dominance distribution. As in the adult, SC neurons in the newborn preferred a moving visual stimulus and had adult-like selectivities for stimulus speed. The developmentally advanced state of the functional circuitry of the newborn monkey SC contrasts with the comparative immaturity of neurons in its visual cortex. It also contrasts with observations on the state of maturation of the newborn SC in other developmental models (e.g., cat). The observation that extensive visual experience is not necessary for the development of many adult-like SC response properties in the monkey SC may help explain the substantial visual capabilities shown by primates soon after birth.


2021 ◽  
Author(s):  
Shinya Ito ◽  
Yufei Si ◽  
Alan M. Litke ◽  
David A. Feldheim

AbstractSensory information from different modalities is processed in parallel, and then integrated in associative brain areas to improve object identification and the interpretation of sensory experiences. The Superior Colliculus (SC) is a midbrain structure that plays a critical role in integrating visual, auditory, and somatosensory input to assess saliency and promote action. Although the response properties of the individual SC neurons to visuoauditory stimuli have been characterized, little is known about the spatial and temporal dynamics of the integration at the population level. Here we recorded the response properties of SC neurons to spatially restricted visual and auditory stimuli using large-scale electrophysiology. We then created a general, population-level model that explains the spatial, temporal, and intensity requirements of stimuli needed for sensory integration. We found that the mouse SC contains topographically organized visual and auditory neurons that exhibit nonlinear multisensory integration. We show that nonlinear integration depends on properties of auditory but not visual stimuli. We also find that a heuristically derived nonlinear modulation function reveals conditions required for sensory integration that are consistent with previously proposed models of sensory integration such as spatial matching and the principle of inverse effectiveness.


2021 ◽  
Vol 17 (11) ◽  
pp. e1009181
Author(s):  
Shinya Ito ◽  
Yufei Si ◽  
Alan M. Litke ◽  
David A. Feldheim

Sensory information from different modalities is processed in parallel, and then integrated in associative brain areas to improve object identification and the interpretation of sensory experiences. The Superior Colliculus (SC) is a midbrain structure that plays a critical role in integrating visual, auditory, and somatosensory input to assess saliency and promote action. Although the response properties of the individual SC neurons to visuoauditory stimuli have been characterized, little is known about the spatial and temporal dynamics of the integration at the population level. Here we recorded the response properties of SC neurons to spatially restricted visual and auditory stimuli using large-scale electrophysiology. We then created a general, population-level model that explains the spatial, temporal, and intensity requirements of stimuli needed for sensory integration. We found that the mouse SC contains topographically organized visual and auditory neurons that exhibit nonlinear multisensory integration. We show that nonlinear integration depends on properties of auditory but not visual stimuli. We also find that a heuristically derived nonlinear modulation function reveals conditions required for sensory integration that are consistent with previously proposed models of sensory integration such as spatial matching and the principle of inverse effectiveness.


2012 ◽  
Vol 35 (11) ◽  
pp. 1738-1752 ◽  
Author(s):  
Robert A. Marino ◽  
Ron Levy ◽  
Susan Boehnke ◽  
Brian J. White ◽  
Laurent Itti ◽  
...  

2013 ◽  
Vol 110 (6) ◽  
pp. 1333-1345 ◽  
Author(s):  
Iain Stitt ◽  
Edgar Galindo-Leon ◽  
Florian Pieper ◽  
Gerhard Engler ◽  
Andreas K. Engel

In the superior colliculus (SC), visual afferent inputs from various sources converge in a highly organized way such that all layers form topographically aligned representations of contralateral external space. Despite this anatomical organization, it remains unclear how the layer-specific termination of different visual input pathways is reflected in the nature of visual response properties and their distribution across layers. To uncover the physiological correlates underlying the laminar organization of the SC, we recorded multiunit and local field potential activity simultaneously from all layers with dual-shank multichannel linear probes. We found that the location of spatial receptive fields was strongly conserved across all visual responsive layers. There was a tendency for receptive field size to increase with depth in the SC, with superficial receptive fields significantly smaller than deep receptive fields. Additionally, superficial layers responded significantly faster than deeper layers to flash stimulation. In some recordings, flash-evoked responses were characterized by the presence of gamma oscillatory activity (40–60 Hz) in multiunit and field potential signals, which was strongest in retinorecipient layers. While SC neurons tended to respond only weakly to full-field drifting gratings, we observed very similar oscillatory responses to the offset of grating stimuli, suggesting gamma oscillations are produced following light offset. Oscillatory spiking activity was highly correlated between horizontally distributed neurons within these layers, with oscillations temporally locked to the stimulus. Together, visual response properties provide physiological evidence reflecting the laminar-specific termination of visual afferent pathways in the SC, most notably characterized by the oscillatory entrainment of superficial neurons.


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