A model for the coordinated development of columnar systems in primate striate cortex

The existence of patchy regions in primate striate cortex in which orientation selectivity is reduced, and which lie in the centers of ocular dominance stripes is well established (Hubel and Livingstone 1981). Analysis of functional maps obtained with voltage sensitive dyes (Blasdel and Salama 1986) has suggested that regions where the spatial rate of change of orientation preference is high, tend to be aligned either along the centers of ocular dominance stripes, or to intersect stripe borders at right angles. In this paper I present results from a developmental model which show that a tendency for orientation selectivity to develop more slowly in the centers of ocular dominance stripes would lead to the observed relationships between the layout of ocular dominance and the map of orientation gradient. This occurs despite the fact that there is no direct connection between the measures of preferred orientation (from which the gradient map is derived) and orientation selectivity (which is independent of preferred orientation). I also show that in both the monkey and the model, orientation singularities have an irregular distribution, but tend to be concentrated in the centers of the ocular dominance stripes. The average density of singularities is about 3/λθ2, where λθ is the period of the orientation columns. The results are based on an elaboration of previous models (Swindale 1980, 1982) which show how, given initially disordered starting conditions, lateral interactions that are short-range excitatory and long-range inhibitory can lead to the development of patterns of orientation or ocular dominance that resemble those found in monkey striate cortex. To explain the coordinated development of the two kinds of column, it is proposed that there is an additional tendency in development for the rate of increase in orientation selectivity to be reduced in the centers of emerging ocular dominance stripes. This might come about if a single factor modulates plasticity in each cell, or column of cells. Thus plasticity may be turned off first in regions in the centers of ocular dominance stripes where relatively extreme and therefore stable ocular dominance values are achieved early in development. Consequently it will be hard for cells in these columns to modify other properties such as orientation preference or selectivity.

[1]  Nicholas V. Swindale,et al.  Coverage and the design of striate cortex , 1991, Biological Cybernetics.

[2]  M. Cynader,et al.  Surface organization of orientation and direction selectivity in cat area 18 , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[3]  N. V. Swindale,et al.  Patches in monkey visual cortex , 1981, Nature.

[4]  E. Switkes,et al.  Functional anatomy of macaque striate cortex. I. Ocular dominance, binocular interactions, and baseline conditions , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[5]  M. Stryker,et al.  Quantitative study of cortical orientation selectivity in visually inexperienced kitten. , 1976, Journal of neurophysiology.

[6]  D. Hubel,et al.  Anatomy and physiology of a color system in the primate visual cortex , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  N. Swindale A model for the formation of ocular dominance stripes , 1980, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[8]  D. Hubel,et al.  The pattern of ocular dominance columns in macaque visual cortex revealed by a reduced silver stain , 1975, The Journal of comparative neurology.

[9]  J. Horton,et al.  Cytochrome oxidase patches: a new cytoarchitectonic feature of monkey visual cortex. , 1984, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[10]  E. Batschelet Circular statistics in biology , 1981 .

[11]  G. Blasdel,et al.  Voltage-sensitive dyes reveal a modular organization in monkey striate cortex , 1986, Nature.

[12]  M. Cynader,et al.  Functional topography in cat area 18 , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  D. Hubel,et al.  The development of ocular dominance columns in normal and visually deprived monkeys , 1980, The Journal of comparative neurology.

[14]  S. Levay,et al.  Ocular dominance columns and their development in layer IV of the cat's visual cortex: A quantitative study , 1978, The Journal of comparative neurology.

[15]  N. Swindale,et al.  A model for the formation of orientation columns , 1982, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[16]  D. Hubel,et al.  Ordered arrangement of orientation columns in monkeys lacking visual experience , 1974, The Journal of comparative neurology.

[17]  D. Hubel,et al.  Regular patchy distribution of cytochrome oxidase staining in primary visual cortex of macaque monkey , 1981, Nature.

[18]  D. Hubel,et al.  Receptive fields and functional architecture of monkey striate cortex , 1968, The Journal of physiology.

[19]  Richard Durbin,et al.  A dimension reduction framework for understanding cortical maps , 1990, Nature.

[20]  R Linsker,et al.  From basic network principles to neural architecture: emergence of orientation-selective cells. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[21]  H. Barlow,et al.  Lack of specificity of neurones in the visual cortex of young kittens. , 1971, The Journal of physiology.

[22]  D H Hubel,et al.  Autoradiographic demonstration of ocular-dominance columns in the monkey striate cortex by means of transneuronal transport. , 1974, Brain research.

[23]  N. Daw,et al.  Comparison of the critical periods for monocular and directional deprivation in cats. , 1977, The Journal of physiology.

[24]  D. Hubel,et al.  Sequence regularity and geometry of orientation columns in the monkey striate cortex , 1974, The Journal of comparative neurology.

[25]  D. Hubel,et al.  Laminar and columnar distribution of geniculo‐cortical fibers in the macaque monkey , 1972, The Journal of comparative neurology.

[26]  D. Hubel,et al.  Uniformity of monkey striate cortex: A parallel relationship between field size, scatter, and magnification factor , 1974, The Journal of comparative neurology.

[27]  D. Hubel,et al.  RECEPTIVE FIELDS OF CELLS IN STRIATE CORTEX OF VERY YOUNG, VISUALLY INEXPERIENCED KITTENS. , 1963, Journal of neurophysiology.

[28]  M. Wong-Riley Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry , 1979, Brain Research.

[29]  D. Hubel,et al.  Plasticity of ocular dominance columns in monkey striate cortex. , 1977, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[30]  A. Hendrickson,et al.  Immunocytochemical localization of glutamic acid decarboxylase in monkey striate cortex , 1981, Nature.

[31]  Michael M. Merzenich,et al.  Changes in endogenous enzymatic reactivity to DAB induced by neuronal inactivity , 1978, Brain Research.

[32]  R Linsker,et al.  From basic network principles to neural architecture: emergence of orientation columns. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[33]  P. Rakić Prenatal development of the visual system in rhesus monkey. , 1977, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[34]  C. Blakemore,et al.  The physiological effects of monocular deprivation and their reversal in the monkey's visual cortex. , 1978, The Journal of physiology.

[35]  D. Hubel,et al.  Anatomical demonstration of orientation columns in macaque monkey , 1978, The Journal of comparative neurology.