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Relation of cortical cell orientation selectivity to alignment of receptive fields of the geniculocortical afferents that arborize within a single orientation column in ferret visual cortex.

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TLDR
Results are consistent with the Hubel and Wiesel (1962) model for the construction of oriented visual cortical receptive fields from geniculate inputs with aligned receptive fields.
Abstract
Neurons in the primary visual cortex of higher mammals are arranged in columns, and the neurons in each column respond best to light-dark borders of particular orientations. The basis of cortical cell orientation selectivity is not known. One possible mechanism would be for cortical cells to receive input from several lateral geniculate nucleus (LGN) neurons with receptive fields that are aligned in the visual field (Hubel and Wiesel, 1962). We have investigated the relationship between the arrangement of the receptive fields of geniculocortical afferents and the orientation preferences of cortical cells in the orientation columns to which the afferents provide visual input. Radial microelectrode penetrations were made into primary visual cortex of anesthetized adult sable ferrets. Cortical cells were recorded throughout the depth of the cortex, and their orientation preferences were determined. Cortical cell responses were then eliminated by superfusion of the cortex with either kainic acid (Zahs and Stryker, 1988) or muscimol. After the drug treatment, responses from many single units with distinct receptive fields were recorded. These responses were presumed to be those of geniculocortical afferents, because they had the response properties characteristic of LGN neurons, and because they could be recorded only in cortical layers that receive geniculate input. In 16 of 18 cases, the afferent receptive fields recorded in a single penetration covered an elongated region of visual space. In these penetrations, the best-fit line through the centers of the afferent receptive fields generally paralleled the preferred orientation of cortical cells recorded at the same site in cortex. These results are consistent with the Hubel and Wiesel (1962) model for the construction of oriented visual cortical receptive fields from geniculate inputs with aligned receptive fields.

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Citations
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Journal ArticleDOI

Theory of orientation tuning in visual cortex.

TL;DR: A simple network model is analytically studied that incorporates both orientation-selective input from the lateral geniculate nucleus and orientation-specific cortical interactions, and exhibits orientation selectivity that originates from within the cortex, by a symmetry-breaking mechanism.
Journal ArticleDOI

Integrated model of visual processing

TL;DR: It is argued that feedback connections are the best candidates for rapid long-distance interconnections between neurons coding for distant regions in the visual field.
Journal ArticleDOI

An emergent model of orientation selectivity in cat visual cortical simple cells

TL;DR: A 1:4 scale model of a 1700 microns by 200 microms region of layer IV of cat primary visual cortex is presented to demonstrate that local intracortical excitation may provide the dominant source of orientation-selective input and provide a unified account of intracellular and extracellular inhibitory blockade experiments that had previously appeared to conflict over the role of inhibition.
Journal ArticleDOI

Specificity of monosynaptic connections from thalamus to visual cortex

TL;DR: This study recorded from thalamic and cortical neurons simultaneously and related their receptive fields to their connectivity, as measured by cross-correlation analysis, implying that the outline of the elongated, simple receptive field, and thus of cortical orientation selectivity, is laid down at the level of the first synapse from the thalami afferents.
Journal ArticleDOI

Functional postnatal development of the rat primary visual cortex and the role of visual experience: Dark rearing and monocular deprivation

TL;DR: To determine the sensitive period of rat visual cortex to MD (critical period), the shift in ODD of visual cortical neurones in rats that were subjected to the progressive delay of the onset of fixed MD period is evaluated.
References
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Journal ArticleDOI

Receptive fields, binocular interaction and functional architecture in the cat's visual cortex

TL;DR: This method is used to examine receptive fields of a more complex type and to make additional observations on binocular interaction and this approach is necessary in order to understand the behaviour of individual cells, but it fails to deal with the problem of the relationship of one cell to its neighbours.
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Plasticity of ocular dominance columns in monkey striate cortex

TL;DR: Preliminary experiments suggest that the layer IVC columns in juvenile macaque monkeys are not fully developed until some weeks after birth, which explains the critical period for deprivation effects in the layerIV columns.
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Columnar specificity of intrinsic horizontal and corticocortical connections in cat visual cortex

TL;DR: The extent of the horizontal connections, which allows single cells to integrate information over larger parts of the visual field than that covered by their receptive fields, and the functional specificity of the connections, suggests possible roles for these connections in visual processing.
Journal ArticleDOI

Receptive fields of cells in striate cortex of very young, visually inexperienced kittens.

TL;DR: The purpose was to learn the age at which cortical cells have normal, adult-type receptive fields, and to find out whether such fields exist even in animals that have had no patterned visual stimulation.
Journal ArticleDOI

Uniformity of monkey striate cortex: a parallel relationship between field size, scatter, and magnification factor.

TL;DR: The term hypercolumn is used to refer to a complete set of either type (180°, or left‐plus‐right eyes), with implications for the topographic mapping of visual fields onto cortex, and receptive‐field size and scatter.
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