scholarly journals Distributed and Retinotopically Asymmetric Processing of Coherent Motion in Mouse Visual Cortex

2019 ◽  
Author(s):  
Kevin K. Sit ◽  
Michael J. Goard
Keyword(s):  
Visual Cortex ◽  
Visual Motion ◽  
Dorsal Stream ◽  
Coherent Motion ◽  
Motion Processing ◽  
Calcium Indicator ◽  
Mouse Cortex ◽  
Visual Areas ◽  
Cortical Regions ◽  
Visual Cortical

ABSTRACTPerception of visual motion is important for a range of ethological behaviors in mammals. In primates, specific higher visual cortical regions are specialized for processing of coherent visual motion. However, the distribution of motion processing among visual cortical areas in mice is unclear, despite the powerful genetic tools available for measuring population neural activity. Here, we used widefield and 2-photon calcium imaging of transgenic mice expressing a calcium indicator in excitatory neurons to measure mesoscale and cellular responses to coherent motion across the visual cortex. Imaging of primary visual cortex (V1) and several higher visual areas (HVAs) during presentation of natural movies and random dot kinematograms (RDKs) revealed heterogeneous responses to coherent motion. Although coherent motion responses were observed throughout visual cortex, particular HVAs in the putative dorsal stream (PM, AL, AM) exhibited stronger responses than ventral stream areas (LM and LI). Moreover, beyond the differences between visual areas, there was considerable heterogeneity within each visual area. Individual visual areas exhibited an asymmetry across the vertical retinotopic axis (visual elevation), such that neurons representing the inferior visual field exhibited greater responses to coherent motion. These results indicate that processing of visual motion in mouse cortex is distributed unevenly across visual areas and exhibits a spatial bias within areas, potentially to support processing of optic flow during spatial navigation.

scholarly journals Structural Differences Across Multiple Visual Cortical Regions in the Absence of Cone Function in Congenital Achromatopsia

2021 ◽  
Vol 15 ◽  
Author(s):  
Rebecca Lowndes ◽  
Barbara Molz ◽  
Lucy Warriner ◽  
Anne Herbik ◽  
Pieter B. de Best ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Surface Area ◽  
Grey Matter Volume ◽  
Cortical Surface ◽  
Colour Perception ◽  
Cortical Surface Area ◽  
Visual Areas ◽  
Cortical Regions ◽  
Visual Cortical ◽  
Cortical Morphology

Most individuals with congenital achromatopsia (ACHM) carry mutations that affect the retinal phototransduction pathway of cone photoreceptors, fundamental to both high acuity vision and colour perception. As the central fovea is occupied solely by cones, achromats have an absence of retinal input to the visual cortex and a small central area of blindness. Additionally, those with complete ACHM have no colour perception, and colour processing regions of the ventral cortex also lack typical chromatic signals from the cones. This study examined the cortical morphology (grey matter volume, cortical thickness, and cortical surface area) of multiple visual cortical regions in ACHM (n = 15) compared to normally sighted controls (n = 42) to determine the cortical changes that are associated with the retinal characteristics of ACHM. Surface-based morphometry was applied to T1-weighted MRI in atlas-defined early, ventral and dorsal visual regions of interest. Reduced grey matter volume in V1, V2, V3, and V4 was found in ACHM compared to controls, driven by a reduction in cortical surface area as there was no significant reduction in cortical thickness. Cortical surface area (but not thickness) was reduced in a wide range of areas (V1, V2, V3, TO1, V4, and LO1). Reduction in early visual areas with large foveal representations (V1, V2, and V3) suggests that the lack of foveal input to the visual cortex was a major driving factor in morphological changes in ACHM. However, the significant reduction in ventral area V4 coupled with the lack of difference in dorsal areas V3a and V3b suggest that deprivation of chromatic signals to visual cortex in ACHM may also contribute to changes in cortical morphology. This research shows that the congenital lack of cone input to the visual cortex can lead to widespread structural changes across multiple visual areas.

Combined Activation and Deactivation of Visual Cortex During Tactile Sensory Processing

2007 ◽  
Vol 97 (2) ◽  
pp. 1633-1641 ◽  
Author(s):  
Lotfi B. Merabet ◽  
Jascha D. Swisher ◽  
Stephanie A. McMains ◽  
Mark A. Halko ◽  
Amir Amedi ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Sensory Processing ◽  
Occipital Cortex ◽  
Visual Modality ◽  
Visual Areas ◽  
Cortical Hierarchy ◽  
Cortical Regions ◽  
Visual Cortical ◽  
Higher Visual Areas ◽  
Significant Activation

The involvement of occipital cortex in sensory processing is not restricted solely to the visual modality. Tactile processing has been shown to modulate higher-order visual and multisensory integration areas in sighted as well as visually deprived subjects; however, the extent of involvement of early visual cortical areas remains unclear. To investigate this issue, we employed functional magnetic resonance imaging in normally sighted, briefly blindfolded subjects with well-defined visuotopic borders as they tactually explored and rated raised-dot patterns. Tactile task performance resulted in significant activation in primary visual cortex (V1) and deactivation of extrastriate cortical regions V2, V3, V3A, and hV4 with greater deactivation in dorsal subregions and higher visual areas. These results suggest that tactile processing affects occipital cortex via two distinct pathways: a suppressive top-down pathway descending through the visual cortical hierarchy and an excitatory pathway arising from outside the visual cortical hierarchy that drives area V1 directly.

Neural correlates of motion processing through echolocation, source hearing, and vision in blind echolocation experts and sighted echolocation novices

2014 ◽  
Vol 111 (1) ◽  
pp. 112-127 ◽  
Author(s):  
L. Thaler ◽  
J. L. Milne ◽  
S. R. Arnott ◽  
D. Kish ◽  
M. A. Goodale
Keyword(s):  
Visual Motion ◽  
Brain Activity ◽  
Region Of Interest ◽  
Occipital Cortex ◽  
Neural Substrates ◽  
Motion Processing ◽  
Planum Temporale ◽  
Show Evidence ◽  
Visual Cortical ◽  
Source Motion

We have shown in previous research (Thaler L, Arnott SR, Goodale MA. PLoS One 6: e20162, 2011) that motion processing through echolocation activates temporal-occipital cortex in blind echolocation experts. Here we investigated how neural substrates of echo-motion are related to neural substrates of auditory source-motion and visual-motion. Three blind echolocation experts and twelve sighted echolocation novices underwent functional MRI scanning while they listened to binaural recordings of moving or stationary echolocation or auditory source sounds located either in left or right space. Sighted participants' brain activity was also measured while they viewed moving or stationary visual stimuli. For each of the three modalities separately (echo, source, vision), we then identified motion-sensitive areas in temporal-occipital cortex and in the planum temporale. We then used a region of interest (ROI) analysis to investigate cross-modal responses, as well as laterality effects. In both sighted novices and blind experts, we found that temporal-occipital source-motion ROIs did not respond to echo-motion, and echo-motion ROIs did not respond to source-motion. This double-dissociation was absent in planum temporale ROIs. Furthermore, temporal-occipital echo-motion ROIs in blind, but not sighted, participants showed evidence for contralateral motion preference. Temporal-occipital source-motion ROIs did not show evidence for contralateral preference in either blind or sighted participants. Our data suggest a functional segregation of processing of auditory source-motion and echo-motion in human temporal-occipital cortex. Furthermore, the data suggest that the echo-motion response in blind experts may represent a reorganization rather than exaggeration of response observed in sighted novices. There is the possibility that this reorganization involves the recruitment of “visual” cortical areas.

scholarly journals Neural selectivity for visual motion in macaque area V3A

2020 ◽  
Author(s):  
Nardin Nakhla ◽  
Yavar Korkian ◽  
Matthew R. Krause ◽  
Christopher C. Pack
Keyword(s):  
Visual Cortex ◽  
Optic Flow ◽  
Functional Role ◽  
Visual Motion ◽  
Flow Patterns ◽  
Brain Regions ◽  
Direction Selectivity ◽  
Motion Processing ◽  
Imaging Studies ◽  
Motion Direction

AbstractThe processing of visual motion is carried out by dedicated pathways in the primate brain. These pathways originate with populations of direction-selective neurons in the primary visual cortex, which project to dorsal structures like the middle temporal (MT) and medial superior temporal (MST) areas. Anatomical and imaging studies have suggested that area V3A might also be specialized for motion processing, but there have been very few studies of single-neuron direction selectivity in this area. We have therefore performed electrophysiological recordings from V3A neurons in two macaque monkeys (one male and one female) and measured responses to a large battery of motion stimuli that includes translation motion, as well as more complex optic flow patterns. For comparison, we simultaneously recorded the responses of MT neurons to the same stimuli. Surprisingly, we find that overall levels of direction selectivity are similar in V3A and MT and moreover that the population of V3A neurons exhibits somewhat greater selectivity for optic flow patterns. These results suggest that V3A should be considered as part of the motion processing machinery of the visual cortex, in both human and non-human primates.Significance statementAlthough area V3A is frequently the target of anatomy and imaging studies, little is known about its functional role in processing visual stimuli. Its contribution to motion processing has been particularly unclear, with different studies yielding different conclusions. We report a detailed study of direction selectivity in V3A. Our results show that single V3A neurons are, on average, as capable of representing motion direction as are neurons in well-known structures like MT. Moreover, we identify a possible specialization for V3A neurons in representing complex optic flow, which has previously been thought to emerge in higher-order brain regions. Thus it appears that V3A is well-suited to a functional role in motion processing.

Pontine projection from striate and prestriate visual cortex in the macaque monkey: An anterograde study

1990 ◽  
Vol 4 (3) ◽  
pp. 205-216 ◽  
Author(s):  
W. Fries
Keyword(s):  
Visual Cortex ◽  
Visual Field ◽  
Striate Cortex ◽  
Macaque Monkey ◽  
Field Of View ◽  
Central Visual Field ◽  
Tracer Techniques ◽  
Visual Areas ◽  
Visual Cortical ◽  
Anterograde Tracer

AbstractThe projection from striate and prestriate visual cortex to the pontine nuclei has been studied in the macaque monkey by means of anterograde tracer techniques in order to assess the contribution of anatomically and functionally distinct visual cortical areas to the cortico-ponto-cerebellar loop. No projection to the pons was found from central or paracentral visual-field representations of V1 (striate cortex) or prestriate visual areas V2, and V4. Small patches of terminal labeling occurred after injections of tracer into more peripheral parts of V1, V2 and V3, and into V3A. The terminal fields were located most dorsolaterally in the anterior to middle third of the pons and were quite restricted in their rostro-caudal extent. Injections of V5, however, yielded substantial terminal labeling, stretching longitudinally throughout almost the entire pons. This projection could be demonstrated to arise from parts of V5 receiving input from central visual-field representations of striate cortex, whereas parts of V4 receiving similarly central visual-field input had no detectable projection to the pons. Its distribution may overlap to a large extent with the termination of tecto-pontine fibers and with the termination of fibers from visual areas in the medial bank (area V6 or P0) and lateral bank (area LIP) of the intraparietal sulcus, as well as from frontal eye fields (FEF). It appears that the main information relayed to the cerebellum by the visual corticopontine projection is related to movement in the field of view.

scholarly journals Biological variation in the sizes, shapes and locations of visual cortical areas in the mouse

2018 ◽  
Author(s):  
Jack Waters ◽  
Eric Lee ◽  
Nathalie Gaudreault ◽  
Fiona Griffin ◽  
Jerome Lecoq ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Visual Information ◽  
Biological Variation ◽  
Measurement Noise ◽  
Cortical Areas ◽  
Retinotopic Maps ◽  
Visual Areas ◽  
Visual Cortical ◽  
Cortical Visual Areas ◽  
Processing Of Visual Information

ABSTRACTVisual cortex is organized into discrete sub-regions or areas that are arranged into a hierarchy and serve different functions in the processing of visual information. In our previous work, we noted that retinotopic maps of cortical visual areas differed between mice, but did not quantify these differences or determine the relative contributions of biological variation and measurement noise. Here we quantify the biological variation in the size, shape and locations of 11 visual areas in the mouse. We find that there is substantial biological variation in the sizes of visual areas, with some visual areas varying in size by two-fold across the population of mice.

scholarly journals Spatial specificity and inheritance of adaptation in human visual cortex

2015 ◽  
Vol 114 (2) ◽  
pp. 1211-1226 ◽  
Author(s):  
Jonas Larsson ◽  
Sarah J. Harrison
Keyword(s):  
Visual Cortex ◽  
Visual Processing ◽  
Visual Motion ◽  
Downstream Processing ◽  
Selective Adaptation ◽  
Motion Direction ◽  
Visual Areas ◽  
Spatial Specificity ◽  
Fmri Adaptation ◽  
The Impact

Adaptation at early stages of sensory processing can be propagated to downstream areas. Such inherited adaptation is a potential confound for functional magnetic resonance imaging (fMRI) techniques that use selectivity of adaptation to infer neuronal selectivity. However, the relative contributions of inherited and intrinsic adaptation at higher cortical stages, and the impact of inherited adaptation on downstream processing, remain unclear. Using fMRI, we investigated how adaptation to visual motion direction and orientation influences visually evoked responses in human V1 and extrastriate visual areas. To dissociate inherited from intrinsic adaptation, we quantified the spatial specificity of adaptation for each visual area as a measure of the receptive field sizes of the area where adaptation originated, predicting that adaptation originating in V1 should be more spatially specific than adaptation intrinsic to extrastriate visual cortex. In most extrastriate visual areas, the spatial specificity of adaptation did not differ from that in V1, suggesting that adaptation originated in V1. Only in one extrastriate area—MT—was the spatial specificity of direction-selective adaptation significantly broader than in V1, consistent with a combination of inherited V1 adaptation and intrinsic MT adaptation. Moreover, inherited adaptation effects could be both facilitatory and suppressive. These results suggest that adaptation at early visual processing stages can have widespread and profound effects on responses in extrastriate visual areas, placing important constraints on the use of fMRI adaptation techniques, while also demonstrating a general experimental strategy for systematically dissociating inherited from intrinsic adaptation by fMRI.

scholarly journals The Contribution of Object Shape and Surface Properties to Object Ensemble Representation in Anterior-medial Ventral Visual Cortex

2017 ◽  
Vol 29 (2) ◽  
pp. 398-412 ◽  
Author(s):  
Jonathan S. Cant ◽  
Yaoda Xu
Keyword(s):  
Visual Cortex ◽  
Surface Properties ◽  
Image Features ◽  
Parahippocampal Gyrus ◽  
Significant Release ◽  
Cortical Regions ◽  
The Individual ◽  
Visual Cortical ◽  
Fmri Adaptation ◽  
Individual Objects

Our visual system can extract summary statistics from large collections of objects without forming detailed representations of the individual objects in the ensemble. In a region in ventral visual cortex encompassing the collateral sulcus and the parahippocampal gyrus and overlapping extensively with the scene-selective parahippocampal place area (PPA), we have previously reported fMRI adaptation to object ensembles when ensemble statistics repeated, even when local image features differed across images (e.g., two different images of the same strawberry pile). We additionally showed that this ensemble representation is similar to (but still distinct from) how visual texture patterns are processed in this region and is not explained by appealing to differences in the color of the elements that make up the ensemble. To further explore the nature of ensemble representation in this brain region, here we used PPA as our ROI and investigated in detail how the shape and surface properties (i.e., both texture and color) of the individual objects constituting an ensemble affect the ensemble representation in anterior-medial ventral visual cortex. We photographed object ensembles of stone beads that varied in shape and surface properties. A given ensemble always contained beads of the same shape and surface properties (e.g., an ensemble of star-shaped rose quartz beads). A change to the shape and/or surface properties of all the beads in an ensemble resulted in a significant release from adaptation in PPA compared with conditions in which no ensemble feature changed. In contrast, in the object-sensitive lateral occipital area (LO), we only observed a significant release from adaptation when the shape of the ensemble elements varied, and found no significant results in additional scene-sensitive regions, namely, the retrosplenial complex and occipital place area. Together, these results demonstrate that the shape and surface properties of the individual objects comprising an ensemble both contribute significantly to object ensemble representation in anterior-medial ventral visual cortex and further demonstrate a functional dissociation between object- (LO) and scene-selective (PPA) visual cortical regions and within the broader scene-processing network itself.

scholarly journals Ventral aspect of the visual form pathway is not critical for the perception of biological motion

2015 ◽  
Vol 112 (4) ◽  
pp. E361-E370 ◽  
Author(s):  
Sharon Gilaie-Dotan ◽  
Ayse Pinar Saygin ◽  
Lauren J. Lorenzi ◽  
Geraint Rees ◽  
Marlene Behrmann
Keyword(s):  
Visual Cortex ◽  
Motion Perception ◽  
Biological Motion ◽  
Form Perception ◽  
Motion Processing ◽  
Extrastriate Body Area ◽  
Biological Motion Perception ◽  
Neurobiological Substrates ◽  
Cortical Regions ◽  
Point Light

Identifying the movements of those around us is fundamental for many daily activities, such as recognizing actions, detecting predators, and interacting with others socially. A key question concerns the neurobiological substrates underlying biological motion perception. Although the ventral “form” visual cortex is standardly activated by biologically moving stimuli, whether these activations are functionally critical for biological motion perception or are epiphenomenal remains unknown. To address this question, we examined whether focal damage to regions of the ventral visual cortex, resulting in significant deficits in form perception, adversely affects biological motion perception. Six patients with damage to the ventral cortex were tested with sensitive point-light display paradigms. All patients were able to recognize unmasked point-light displays and their perceptual thresholds were not significantly different from those of three different control groups, one of which comprised brain-damaged patients with spared ventral cortex (n > 50). Importantly, these six patients performed significantly better than patients with damage to regions critical for biological motion perception. To assess the necessary contribution of different regions in the ventral pathway to biological motion perception, we complement the behavioral findings with a fine-grained comparison between the lesion location and extent, and the cortical regions standardly implicated in biological motion processing. This analysis revealed that the ventral aspects of the form pathway (e.g., fusiform regions, ventral extrastriate body area) are not critical for biological motion perception. We hypothesize that the role of these ventral regions is to provide enhanced multiview/posture representations of the moving person rather than to represent biological motion perception per se.

scholarly journals Multimodal Imaging Evidence for a Frontoparietal Modulation of Visual Cortex during the Selective Processing of Conditioned Threat

2017 ◽  
Vol 29 (6) ◽  
pp. 953-967 ◽  
Author(s):  
Nathan M. Petro ◽  
L. Forest Gruss ◽  
Siyang Yin ◽  
Haiqing Huang ◽  
Vladimir Miskovic ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Large Scale ◽  
Anterior Insula ◽  
Causal Modeling ◽  
Middle Frontal Gyrus ◽  
Large Scale Network ◽  
Inferior Parietal Cortex ◽  
Scale Network ◽  
Cortical Regions ◽  
Visual Cortical

Emotionally salient cues are detected more readily, remembered better, and evoke greater visual cortical responses compared with neutral stimuli. The current study used concurrent EEG-fMRI recordings to identify large-scale network interactions involved in the amplification of visual cortical activity when viewing aversively conditioned cues. To generate a continuous neural signal from pericalcarine visual cortex, we presented rhythmic (10/sec) phase-reversing gratings, the orientation of which predicted the presence (CS+) or absence (CS−) of a cutaneous electric shock (i.e., the unconditioned stimulus). The resulting single trial steady-state visual evoked potential (ssVEP) amplitude was regressed against the whole-brain BOLD signal, resulting in a measure of ssVEP-BOLD coupling. Across all trial types, ssVEP-BOLD coupling was observed in both primary and extended visual cortical regions, the rolandic operculum, as well as the thalamus and bilateral hippocampus. For CS+ relative to CS− trials during the conditioning phase, BOLD-alone analyses showed CS+ enhancement at the occipital pole, superior temporal sulci, and the anterior insula bilaterally, whereas ssVEP-BOLD coupling was greater in the pericalcarine cortex, inferior parietal cortex, and middle frontal gyrus. Dynamic causal modeling analyses supported connectivity models in which heightened activity in pericalcarine cortex for threat (CS+) arises from cortico-cortical top–down modulation, specifically from the middle frontal gyrus. No evidence was observed for selective pericalcarine modulation by deep cortical structures such as the amygdala or anterior insula, suggesting that the heightened engagement of pericalcarine cortex for threat stimuli is mediated by cortical structures that constitute key nodes of canonical attention networks.

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