Orientation Selectivity and the Arrangement of Horizontal Connections in Tree Shrew Striate Cortex

Horizontal connections, formed primarily by the axon collaterals of pyramidal neurons in layer 2/3 of visual cortex, extend for millimeters parallel to the cortical surface and form patchy terminations. Previous studies have provided evidence that the patches formed by horizontal connections exhibit modular specificity, preferentially linking columns of neurons with similar response characteristics, such as preferred orientation. The issue of how these connections are distributed with respect to the topographic map of visual space, however, has not been resolved. Here we combine optical imaging of intrinsic signals with small extracellular injections of biocytin to assess quantitatively the specificity of horizontal connections with respect to both the map of orientation preference and the map of visual space in tree shrew V1. Our results indicate that horizontal connections outside a radius of 500 μm from the injection site exhibit not only modular specificity, but also specificity for axis of projection. Labeled axons extend for longer distances, and give off more terminal boutons, along an axis in the map of visual space that corresponds to the preferred orientation of the injection site. Inside of 500 μm, the pattern of connections is much less specific, with boutons found along every axis, contacting sites with a wide range of preferred orientations. The system of long-range horizontal connections can be summarized as preferentially linking neurons with co-oriented, co-axially aligned receptive fields. These observations suggest specific ways that horizontal circuits contribute to the response properties of layer 2/3 neurons and to mechanisms of visual perception.

[1]  D. Hubel,et al.  Receptive fields, binocular interaction and functional architecture in the cat's visual cortex , 1962, The Journal of physiology.

[2]  W. C. Hall,et al.  Visual cortex of the tree shrew (Tupaia glis): architectonic subdivisions and representations of the visual field. , 1972, Brain research.

[3]  P. O. Bishop,et al.  Orientation specificity of cells in cat striate cortex. , 1974, Journal of neurophysiology.

[4]  T. Wiesel,et al.  Morphology and intracortical projections of functionally characterised neurones in the cat visual cortex , 1979, Nature.

[5]  A L Humphrey,et al.  Topographic organization of the orientation column system in the striate cortex of the tree shrew (Tupaia glis). II. Deoxyglucose mapping , 1980, The Journal of comparative neurology.

[6]  Jon H. Kaas,et al.  A Comparative Survey of Visual Cortex Organization in Mammals , 1980 .

[7]  A. L. Humphrey,et al.  Topographic organization of the orientation column system in the striate cortex of the tree shrew (Tupaia glis). I. Microelectrode recording , 1980, The Journal of comparative neurology.

[8]  G. Mitchison,et al.  Long axons within the striate cortex: their distribution, orientation, and patterns of connection. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[9]  J. Lund,et al.  Widespread periodic intrinsic connections in the tree shrew visual cortex. , 1982, Science.

[10]  T. Wiesel,et al.  Clustered intrinsic connections in cat visual cortex , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  D. Hubel,et al.  Specificity of intrinsic connections in primate primary visual cortex , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  M. Cynader,et al.  Intrinsic projections within visual cortex: evidence for orientation-specific local connections. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[13]  T. Wiesel,et al.  Relationships between horizontal interactions and functional architecture in cat striate cortex as revealed by cross-correlation analysis , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  T. Wiesel,et al.  Functional architecture of cortex revealed by optical imaging of intrinsic signals , 1986, Nature.

[15]  M. Cynader,et al.  Anatomical properties and physiological correlates of the intrinsic connections in cat area 18 , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  Charles D. Gilbert,et al.  The Role of Horizontal Connections in Generating Long Receptive Fields in the Cat Visual Cortex , 1989, The European journal of neuroscience.

[17]  T. Wiesel,et al.  Columnar specificity of intrinsic horizontal and corticocortical connections in cat visual cortex , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  Amiram Grinvald,et al.  Iso-orientation domains in cat visual cortex are arranged in pinwheel-like patterns , 1991, Nature.

[19]  T. Wiesel,et al.  Targets of horizontal connections in macaque primary visual cortex , 1991, The Journal of comparative neurology.

[20]  U. Eysel,et al.  Cellular organization of reciprocal patchy networks in layer III of cat visual cortex (area 17) , 1992, Neuroscience.

[21]  J. Boyd,et al.  Presence of GABA-immunoreactive neurons within intracortical patches in area 18 of the cat , 1992, Brain Research.

[22]  C. Gilbert Horizontal integration and cortical dynamics , 1992, Neuron.

[23]  G. Blasdel,et al.  Orientation selectivity, preference, and continuity in monkey striate cortex , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[24]  R Gattass,et al.  Dynamic surrounds of receptive fields in primate striate cortex: a physiological basis for perceptual completion? , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[25]  M. Stryker,et al.  Development of orientation selectivity in ferret visual cortex and effects of deprivation , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  U. Polat,et al.  Lateral interactions between spatial channels: Suppression and facilitation revealed by lateral masking experiments , 1993, Vision Research.

[27]  A. Grinvald,et al.  The layout of iso-orientation domains in area 18 of cat visual cortex: optical imaging reveals a pinwheel-like organization , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[28]  A. Grinvald,et al.  Relationship between intrinsic connections and functional architecture revealed by optical imaging and in vivo targeted biocytin injections in primate striate cortex. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[29]  David J. Field,et al.  Contour integration by the human visual system: Evidence for a local “association field” , 1993, Vision Research.

[30]  U. Eysel,et al.  Functional and Structural Topography of Horizontal Inhibitory Connections in Cat Visual Cortex , 1993, The European journal of neuroscience.

[31]  K. Obermayer,et al.  Geometry of orientation and ocular dominance columns in monkey striate cortex , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  R. Malach,et al.  Cortical hierarchy reflected in the organization of intrinsic connections in macaque monkey visual cortex , 1993, The Journal of comparative neurology.

[33]  R. Frostig,et al.  Cortical point-spread function and long-range lateral interactions revealed by real-time optical imaging of macaque monkey primary visual cortex , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[34]  T. Bonhoeffer,et al.  Relationship Between Lateral Inhibitory Connections and the Topography of the Orientation Map in Cat Visual Cortex , 1994, The European journal of neuroscience.

[35]  K. Albus,et al.  The Topography of Tangential Inhibitory Connections in the Postnatally Developing and Mature Striate Cortex of the Cat , 1994, The European journal of neuroscience.

[36]  D. Fitzpatrick,et al.  Patterns of excitation and inhibition evoked by horizontal connections in visual cortex share a common relationship to orientation columns , 1995, Neuron.

[37]  C. Gilbert,et al.  Improvement in visual sensitivity by changes in local context: Parallel studies in human observers and in V1 of alert monkeys , 1995, Neuron.

[38]  D. Fitzpatrick,et al.  Specificity in the axonal connections of layer VI neurons in tree shrew striate cortex: evidence for distinct granular and supragranular systems , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.