scholarly journals Context-dependent signaling of coincident auditory and visual events in primary visual cortex

2018 ◽  
Author(s):  
Thomas Deneux ◽  
Alexandre Kempf ◽  
Brice Bathellier
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Calcium Imaging ◽  
Cell Types ◽  
Visual Responses ◽  
Sound Sources ◽  
Two Photon ◽  
Visual Events ◽  
Visual Inputs ◽  
Sensory Modalities

AbstractDetecting rapid coincident changes across sensory modalities is essential to recognize sudden threats and events. Using two-photon calcium imaging in identified cell types in awake mice, we show that auditory cortex (AC) neurons projecting to primary visual cortex (V1) preferentially encode the abrupt onsets of sounds. In V1, a sub-population of layer 1 interneurons gates this selective cross-modal information by a suppression specific to the absence of visual inputs. However, when large auditory onsets coincide with visual stimuli, visual responses are strongly boosted in V1. Thus, a dynamic asymmetric circuit across AC and V1 specifically identifies visual events starting simultaneously to sudden sounds, potentially catalyzing localization of new sound sources in the visual field.

scholarly journals Context-dependent signaling of coincident auditory and visual events in primary visual cortex

eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Thomas Deneux ◽  
Evan R Harrell ◽  
Alexandre Kempf ◽  
Sebastian Ceballo ◽  
Anton Filipchuk ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Auditory Cortex ◽  
Primary Visual Cortex ◽  
Cell Types ◽  
Dependent Manner ◽  
Visual Responses ◽  
Loud Sound ◽  
Visual Events ◽  
Dominant Feature ◽  
Context Dependent

Detecting rapid, coincident changes across sensory modalities is essential for recognition of sudden threats or events. Using two-photon calcium imaging in identified cell types in awake, head-fixed mice, we show that, among the basic features of a sound envelope, loud sound onsets are a dominant feature coded by the auditory cortex neurons projecting to primary visual cortex (V1). In V1, a small number of layer 1 interneurons gates this cross-modal information flow in a context-dependent manner. In dark conditions, auditory cortex inputs lead to suppression of the V1 population. However, when sound input coincides with a visual stimulus, visual responses are boosted in V1, most strongly after loud sound onsets. Thus, a dynamic, asymmetric circuit connecting AC and V1 contributes to the encoding of visual events that are coincident with sounds.

scholarly journals Chromatic micromaps in primary visual cortex

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Soumya Chatterjee ◽  
Kenichi Ohki ◽  
R. Clay Reid
Keyword(s):  
Fine Structure ◽  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Calcium Imaging ◽  
Similar Response ◽  
Functional Architecture ◽  
Color Representation ◽  
Two Photon ◽  
Layer 2 ◽  
Spatial Content

AbstractThe clustering of neurons with similar response properties is a conspicuous feature of neocortex. In primary visual cortex (V1), maps of several properties like orientation preference are well described, but the functional architecture of color, central to visual perception in trichromatic primates, is not. Here we used two-photon calcium imaging in macaques to examine the fine structure of chromatic representation and found that neurons responsive to spatially uniform, chromatic stimuli form unambiguous clusters that coincide with blobs. Further, these responsive groups have marked substructure, segregating into smaller ensembles or micromaps with distinct chromatic signatures that appear columnar in upper layer 2/3. Spatially structured chromatic stimuli revealed maps built on the same micromap framework but with larger subdomains that go well beyond blobs. We conclude that V1 has an architecture for color representation that switches between blobs and a combined blob/interblob system based on the spatial content of the visual scene.

Mapping receptive fields on mouse primary visual cortex: reverse correlation using two-photon calcium imaging signals

2009 ◽  
Vol 65 ◽  
pp. S172
Author(s):  
Yoshiya Mori ◽  
Koji Ikezoe ◽  
Junichi Furutaka ◽  
Kazuo Kitamura ◽  
Hiroshi Tamura ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Calcium Imaging ◽  
Receptive Fields ◽  
Reverse Correlation ◽  
Two Photon

scholarly journals Deficits in higher visual area representations in a mouse model of Angelman syndrome

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Leah B. Townsend ◽  
Kelly A. Jones ◽  
Christopher R. Dorsett ◽  
Benjamin D. Philpot ◽  
Spencer L. Smith
Keyword(s):  
Visual Cortex ◽  
Mouse Model ◽  
Primary Visual Cortex ◽  
Angelman Syndrome ◽  
Calcium Imaging ◽  
Neurodevelopmental Disorders ◽  
Synaptic Function ◽  
Strong Response ◽  
Intrinsic Signal ◽  
Two Photon

Abstract Background Sensory processing deficits are common in individuals with neurodevelopmental disorders. One hypothesis is that deficits may be more detectable in downstream, “higher” sensory areas. A mouse model of Angelman syndrome (AS), which lacks expression of the maternally inherited Ube3a allele, has deficits in synaptic function and experience-dependent plasticity in the primary visual cortex. Thus, we hypothesized that AS model mice have deficits in visually driven neuronal responsiveness in downstream higher visual areas (HVAs). Methods Here, we used intrinsic signal optical imaging and two-photon calcium imaging to map visually evoked neuronal activity in the primary visual cortex and HVAs in response to an array of stimuli. Results We found a highly specific deficit in HVAs. Drifting gratings that changed speed caused a strong response in HVAs in wildtype mice, but this was not observed in littermate AS model mice. Further investigation with two-photon calcium imaging revealed the effect to be largely driven by aberrant responses of inhibitory interneurons, suggesting a cellular basis for higher level, stimulus-selective cortical dysfunction in AS. Conclusion Assaying downstream, or “higher” circuitry may provide a more sensitive measure for circuit dysfunction in mouse models of neurodevelopmental disorders. Trial registration Not applicable.

scholarly journals Astrocytes in the mouse visual cortex reliably respond to visual stimulation

2018 ◽  
Author(s):  
Keita Sonoda ◽  
Teppei Matsui ◽  
Haruhiko Bito ◽  
Kenichi Ohki
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Common Mechanism ◽  
List Type ◽  
Visual Responses ◽  
Two Photon ◽  
Dual Color ◽  
Cross Correlation Analysis ◽  
Mouse Visual Cortex

AbstractAstrocytes are known to contact with a great number of synapses and may integrate sensory inputs. In the ferret primary visual cortex, astrocytes respond to a visual stimulus with a delay of several seconds with respect to the surrounding neurons. However, in the mouse visual cortex, it remains unclear whether astrocytes respond to visual stimulations. In this study, using dual-color simultaneous in vivo two-photon Ca2+ imaging of neurons and astrocytes in the awake mouse visual cortex, we examined the visual responsiveness of astrocytes and their precise response timing relative to the surrounding neurons. Neurons reliably responded to visual stimulations, whereas astrocytes often showed neuromodulator-mediated global activities, which largely masked small periodic activities. Administration of the selective α1-adrenergic receptor antagonist prazosin substantially reduced such global astrocytic activities without affecting the neuronal visual responses. In the presence of prazosin, astrocytes showed weak but consistent visual responses mostly at their somata. Cross-correlation analysis estimated that the astrocytic visual responses were delayed by approximately 5 s relative to the surrounding neuronal responses. In conclusion, our research demonstrated that astrocytes in the primary visual cortex of awake mice responded to visual stimuli with a delay of several seconds relative to the surrounding neurons, which may indicate the existence of a common mechanism of neuron–astrocyte communication across species.HighlightsWe performed dual-color in vivo two-photon Ca2+ imaging of neurons and astrocytes.α1-adrenoblocker prazosin substantially reduced global astrocytic activities.Astrocytes showed weak but reliable visual responses in the awake mouse visual cortex.Astrocytic visual responses were delayed by 5 s relative to the neuronal ones.

scholarly journals Color and orientation are jointly coded and spatially organized in primate primary visual cortex

Science ◽  
2019 ◽  
Vol 364 (6447) ◽  
pp. 1275-1279 ◽  
Author(s):  
Anupam K. Garg ◽  
Peichao Li ◽  
Mohammad S. Rashid ◽  
Edward M. Callaway
Keyword(s):  
Visual Cortex ◽  
Single Cell ◽  
Primary Visual Cortex ◽  
Visual Stimulus ◽  
Calcium Imaging ◽  
Stimulus Space ◽  
Single Neurons ◽  
V1 Neurons ◽  
Two Photon ◽  
Rigorous Testing

Previous studies support the textbook model that shape and color are extracted by distinct neurons in primate primary visual cortex (V1). However, rigorous testing of this model requires sampling a larger stimulus space than previously possible. We used stable GCaMP6f expression and two-photon calcium imaging to probe a very large spatial and chromatic visual stimulus space and map functional microarchitecture of thousands of neurons with single-cell resolution. Notable proportions of V1 neurons strongly preferred equiluminant color over achromatic stimuli and were also orientation selective, indicating that orientation and color in V1 are mutually processed by overlapping circuits. Single neurons could precisely and unambiguously code for both color and orientation. Further analyses revealed systematic spatial relationships between color tuning, orientation selectivity, and cytochrome oxidase histology.

scholarly journals Binocular integration of retinal motion information underlies optic flow processing by the cortex

2020 ◽  
Author(s):  
Rune N. Rasmussen ◽  
Akihiro Matsumoto ◽  
Simon Arvin ◽  
Keisuke Yonehara
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Optic Flow ◽  
Calcium Imaging ◽  
Direction Selectivity ◽  
Motion Information ◽  
Two Photon ◽  
Retinal Motion ◽  
Visual Areas ◽  
Higher Visual Areas

AbstractLocomotion creates various patterns of optic flow on the retina, which provide the observer with information about their movement relative to the environment. However, it is unclear how these optic flow patterns are encoded by the cortex. Here we use two-photon calcium imaging in awake mice to systematically map monocular and binocular responses to horizontal motion in four areas of the visual cortex. We find that neurons selective to translational or rotational optic flow are abundant in higher visual areas, whereas neurons suppressed by binocular motion are more common in the primary visual cortex. Disruption of retinal direction selectivity in Frmd7 mutant mice reduces the number of translation-selective neurons in the primary visual cortex, and translation- and rotation-selective neurons as well as binocular direction-selective neurons in the rostrolateral and anterior visual cortex, blurring the functional distinction between primary and higher visual areas. Thus, optic flow representations in specific areas of the visual cortex rely on binocular integration of motion information from the retina.

scholarly journals “Real-time” obstacle avoidance in the absence of primary visual cortex

2009 ◽  
Vol 106 (37) ◽  
pp. 15996-16001 ◽  
Author(s):  
Christopher L. Striemer ◽  
Craig S. Chapman ◽  
Melvyn A. Goodale
Keyword(s):  
Visual Cortex ◽  
Real Time ◽  
Obstacle Avoidance ◽  
Primary Visual Cortex ◽  
Posterior Parietal Cortex ◽  
Dorsal Stream ◽  
Visual Pathways ◽  
Visual Stream ◽  
Reaching Task ◽  
Visual Inputs

When we reach toward objects, we easily avoid potential obstacles located in the workspace. Previous studies suggest that obstacle avoidance relies on mechanisms in the dorsal visual stream in the posterior parietal cortex. One fundamental question that remains unanswered is where the visual inputs to these dorsal-stream mechanisms are coming from. Here, we provide compelling evidence that these mechanisms can operate in “real-time” without direct input from primary visual cortex (V1). In our first experiment, we used a reaching task to demonstrate that an individual with a dense left visual field hemianopia after damage to V1 remained strikingly sensitive to the position of unseen static obstacles placed in his blind field. Importantly, in a second experiment, we showed that his sensitivity to the same obstacles in his blind field was abolished when a short 2-s delay (without vision) was introduced before reach onset. These findings have far-reaching implications, not only for our understanding of the time constraints under which different visual pathways operate, but also in relation to how these seemingly “primitive” subcortical visual pathways can control complex everyday behavior without recourse to conscious vision.

scholarly journals 3D Ultrastructure of Synaptic Inputs to Distinct GABAergic Neurons in the Mouse Primary Visual Cortex

2020 ◽  
Author(s):  
Yang-Sun Hwang ◽  
Catherine Maclachlan ◽  
Jérôme Blanc ◽  
Anaëlle Dubois ◽  
Carl C H Petersen ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Pyramidal Neuron ◽  
Cell Types ◽  
Gabaergic Neurons ◽  
Inhibitory Synapses ◽  
Synaptic Inputs ◽  
Neuronal Types ◽  
The Difference ◽  
Ultrastructure Of Synapses

Abstract Synapses are the fundamental elements of the brain’s complicated neural networks. Although the ultrastructure of synapses has been extensively studied, the difference in how synaptic inputs are organized onto distinct neuronal types is not yet fully understood. Here, we examined the cell-type-specific ultrastructure of proximal processes from the soma of parvalbumin-positive (PV+) and somatostatin-positive (SST+) GABAergic neurons in comparison with a pyramidal neuron in the mouse primary visual cortex (V1), using serial block-face scanning electron microscopy. Interestingly, each type of neuron organizes excitatory and inhibitory synapses in a unique way. First, we found that a subset of SST+ neurons are spiny, having spines on both soma and dendrites. Each of those spines has a highly complicated structure that has up to eight synaptic inputs. Next, the PV+ and SST+ neurons receive more robust excitatory inputs to their perisoma than does the pyramidal neuron. Notably, excitatory synapses on GABAergic neurons were often multiple-synapse boutons, making another synapse on distal dendrites. On the other hand, inhibitory synapses near the soma were often single-targeting multiple boutons. Collectively, our data demonstrate that synaptic inputs near the soma are differentially organized across cell types and form a network that balances inhibition and excitation in the V1.

scholarly journals Morphological and Physiological Characterization of Layer VI Corticofugal Neurons of Mouse Primary Visual Cortex

2003 ◽  
Vol 89 (5) ◽  
pp. 2854-2867 ◽  
Author(s):  
Joshua C. Brumberg ◽  
Farid Hamzei-Sichani ◽  
Rafael Yuste
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Action Potentials ◽  
Three Dimensional ◽  
Cell Types ◽  
Dorsal Lateral Geniculate Nucleus ◽  
Morphological Properties ◽  
Feedback Connection ◽  
Physiological Characterization ◽  
Layer Vi

Layer VI is the origin of the massive feedback connection from the cortex to the thalamus, yet its complement of cell types and their connections is poorly understood. The physiological and morphological properties of corticofugal neurons of layer VI of mouse primary visual cortex were investigated in slices loaded with the Ca2+indicator fura-2AM. To identify corticofugal neurons, electrical stimulation of the white matter (WM) was done in conjunction with calcium imaging to detect neurons that responded with changes in intracellular Ca2+ concentrations in response to the stimulation. Subsequent whole cell recordings confirmed that they discharged antidromic action potentials after WM stimulation. Antidromically activated neurons were more excitable and had different spiking properties than neighboring nonantidromic neurons, although both groups had similar input resistances. Furthermore, antidromic neurons possessed narrower action potentials and smaller afterhyperpolarizations. Additionally, three-dimensional reconstructions indicated that antidromically activated neurons had a distinct morphology with longer apical dendrites and fewer nonprimary dendrites than nonantidromic cells. To identify the antidromic neurons, rhodamine microspheres were injected into the dorsal lateral geniculate nucleus of the thalamus and allowed to retrogradely transport back to the somata of the layer VI cortico-geniculate neurons. Physiological and anatomical analysis indicated that most antidromic neurons were likely to be cortico-geniculate neurons. Our results show that cortico-thalamic neurons represent a specific functional and morphological class of layer VI neurons.

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