A role for action-potential activity in the development of neuronal connections in the kitten retinogeniculate pathway

The role of action potentials in the development of proper synaptic connections in the mammalian CNS was studied in the kitten retinogeniculate pathway. Our basic finding is that there is improper segregation of retinal inputs onto LGN cells after prolonged retinal action-potential blockade. Retinal ganglion cell firing was silenced from birth by repeated monocular injections of TTX. The resulting ganglion cell connections in the LGN were studied electrophysiologically after the action-potential blockade was ended. Most cells in the deprived LGN layers received excitatory input from both ON-center and OFF-center type ganglion cells, whereas LGN cells normally receive inputs only from ON-center or OFF-center ganglion cells, but not from both types. Improper segregation of ON and OFF inputs has never been reported after other types of visual deprivation that do not block ganglion cell activity. Control experiments showed that receptive fields in the nondeprived LGN layers were normal, that ganglion cell responses remained normal, and that there was no obvious ganglion cell loss. We also showed that individual LGN cells with ON and OFF excitatory inputs were not present in normal neonatal kittens. Two other types of improper input segregation in response to action- potential blockade were also found in the deprived LGN layers. (1) A greater than normal number of LGN cells received both X- and Y-type ganglion cell input. (2) Almost half of the cells at LGN layer borders were excited binocularly. Recovery of LGN normality was rapid and complete after blockade that lasted for only 3 weeks from birth, but little recovery was seen after about 11 weeks of blockade. The susceptibility to action-potential blockade decreased during the first 3 postnatal weeks. These findings may result from axon-terminal sprouting or from the failure of axon terminals to retract. The results are consistent with the idea that normally synchronous activity of neighboring ganglion cells of like center-type may be used in the refinement of retinogeniculate synaptic connections.

[1]  M. Dubin,et al.  Response properties of neurons in the lateral geniculate nucleus of neonatal kittens , 1986, Vision Research.

[2]  M. Stryker,et al.  Binocular impulse blockade prevents the formation of ocular dominance columns in cat visual cortex , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[3]  James W. Fawcett,et al.  The role of electrical activity in the formation of topographic maps in the nervous system , 1985, Trends in Neurosciences.

[4]  M. Constantine-Paton,et al.  Eye-specific segregation requires neural activity in three-eyed Rana pipiens , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[5]  D. Sanes,et al.  The sharpening of frequency tuning curves requires patterned activity during development in the mouse, Mus musculus , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[6]  J. Schmidt,et al.  Activity and the formation of ocular dominance patches in dually innervated tectum of goldfish , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  J. Fawcett,et al.  Regressive events in neurogenesis. , 1984, Science.

[8]  W M Cowan,et al.  Activity and the control of ganglion cell death in the rat retina. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[9]  D. Mastronarde,et al.  Organization of the cat's optic tract as assessed by single‐axon recordings , 1984, The Journal of comparative neurology.

[10]  W. Thompson,et al.  Fibre type composition of single motor units during synapse elimination in neonatal rat soleus muscle , 1984, Nature.

[11]  D. Edwards,et al.  Intraocular injection of tetrodotoxin in goldfish decreases fast axonal transport of [3H]glucosamine-labeled materials in optic axons , 1984, Brain Research.

[12]  C. Shatz,et al.  Prenatal development of functional connections in the cat's retinogeniculate pathway , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  C. R. Michael,et al.  Terminal patterns of single, physiologically characterized optic tract fibers in the cat's lateral geniculate nucleus , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  M. Constantine‐Paton Position and proximity in the development of maps and stripes , 1983, Trends in Neurosciences.

[15]  D. Purves Modulation of neuronal competition by postsynaptic geometry in autonomic ganglia , 1983, Trends in Neurosciences.

[16]  T. Kasamatsu,et al.  Changes in geniculate cell size following brief monocular blockade of retinal activity in kittens , 1983, Nature.

[17]  Adam M. Sillito,et al.  The influence of GABAergic inhibitory processes on the receptive field structure of X and Y cells in cat dorsal lateral geniculate nucleus (dLGN) , 1983, Brain Research.

[18]  D. Sanes,et al.  Altered activity patterns during development reduce neural tuning. , 1983, Science.

[19]  D. Edwards,et al.  Intraocular tetrodotoxin in goldfish hinders optic nerve regeneration , 1983, Brain Research.

[20]  J. Schmidt,et al.  Activity sharpens the map during the regeneration of the retinotectal projection in goldfish , 1983, Brain Research.

[21]  C. Shatz The prenatal development of the cat's retinogeniculate pathway , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[22]  M. Wong-Riley,et al.  The effect of impulse blockage on cytochrome oxidase activity in the cat visual system , 1983, Brain Research.

[23]  D. Mastronarde Correlated firing of cat retinal ganglion cells. II. Responses of X- and Y-cells to single quantal events. , 1983, Journal of neurophysiology.

[24]  R L Meyer,et al.  Tetrodotoxin inhibits the formation of refined retinotopography in goldfish. , 1983, Brain research.

[25]  D. Mastronarde Correlated firing of cat retinal ganglion cells. I. Spontaneously active inputs to X- and Y-cells. , 1983, Journal of neurophysiology.

[26]  S. Udin,et al.  Abnormal visual input leads to development of abnormal axon trajectories in frogs , 1983, Nature.

[27]  M J Bastiani,et al.  Loss of axons in the cat optic nerve following fetal unilateral enucleation: an electron microscopic analysis , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[28]  John T. Schmidt The formation of retinotectal projections , 1982, Trends in Neurosciences.

[29]  K. Kratz Spatial and temporal sensitivity of lateral geniculate cells in dark-reared cats , 1982, Brain Research.

[30]  R L Meyer,et al.  Tetrodotoxin blocks the formation of ocular dominance columns in goldfish. , 1982, Science.

[31]  J. Stone,et al.  The optic nerve of the cat: appearance and loss of axons during normal development. , 1982, Brain research.

[32]  S M Archer,et al.  Abnormal development of kitten retino-geniculate connectivity in the absence of action potentials. , 1982, Science.

[33]  S. Sherman,et al.  Organization of visual pathways in normal and visually deprived cats. , 1982, Physiological reviews.

[34]  M. J. Friedlander,et al.  Morphology of functionally identified neurons in lateral geniculate nucleus of the cat. , 1981, Journal of neurophysiology.

[35]  F. Duffy,et al.  The effects of dark-rearing on the development and plasticity of the lateral geniculate nucleus. , 1981, Brain research.

[36]  T. Powell,et al.  A quantitative electron-microscopical study of the postnatal development of the lateral geniculate nucleus in normal kittens and in kittens with eyelid suture , 1980, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[37]  T. Powell,et al.  An electron-microscopical study of the postnatal development of the lateral geniculate nucleus in the normal kitten and after eyelid suture , 1980, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[38]  D. Purves,et al.  Elimination of synapses in the developing nervous system. , 1980, Science.

[39]  R. Kalil A quantitative study of the effects of monocular enucleation and deprivation on cell growth in the dorsal lateral geniculate nucleus of the cat , 1980 .

[40]  M. Dubin,et al.  Inteneuron circuits in the lateral geniculate nucleus of monocularly deprived cats , 1979 .

[41]  J. K. S. Jansen,et al.  The effect of prolonged, reversible block of nerve impulses on the elimination of polyneuronal innervation of new-born rat skeletal muscle fibers , 1979, Neuroscience.

[42]  R. Kalil Development of the dorsal lateral geniculate nucleus in the cat , 1978, The Journal of comparative neurology.

[43]  M. Law,et al.  Eye-specific termination bands in tecta of three-eyed frogs. , 1978, Science.

[44]  J. Pettigrew,et al.  Development of single-neuron responses in kitten's lateral geniculate nucleus. , 1978, Journal of neurophysiology.

[45]  J. Stone,et al.  The number and distribution of ganglion cells in the cat's retina , 1978, The Journal of comparative neurology.

[46]  J. Changeux,et al.  Consequences of blocking the nerve with a local anaesthetic on the evolution of multiinnervation at the regenerating neuromuscular junction of the rat , 1978, Brain Research.

[47]  PETER E. LOWTHER,et al.  In Memory , 1977, Evolution; international journal of organic evolution.

[48]  Rusoff Ac,et al.  Development of receptive-field properties of retinal ganglion cells in kittens. , 1977 .

[49]  B. Cleland,et al.  Organization of visual inputs to interneurons of lateral geniculate nucleus of the cat. , 1977, Journal of neurophysiology.

[50]  J. Changeux,et al.  Selective stabilisation of developing synapses as a mechanism for the specification of neuronal networks , 1976, Nature.

[51]  C. Malsburg,et al.  How patterned neural connections can be set up by self-organization , 1976, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[52]  R. Shapley,et al.  Quantitative analysis of retinal ganglion cell classifications. , 1976, The Journal of physiology.

[53]  A Hughes,et al.  A quantitative analysis of the cat retinal ganglion cell topography , 1975, The Journal of comparative neurology.

[54]  B. Cragg,et al.  The development of synapses in the visual system of the cat , 1975, The Journal of comparative neurology.

[55]  H. Wässle,et al.  The distribution of the alpha type of ganglion cells in the cat's retina , 1975, The Journal of comparative neurology.

[56]  R. Guillery,et al.  Behavioral, electrophysiological and morphological studies of binocular competition in the development of the geniculo–corticalpathways of cats , 1974, The Journal of comparative neurology.

[57]  R. Kalil,et al.  Dissociation of retinal fibers by degeneration rate. , 1974, Brain Research.

[58]  G. Stent A physiological mechanism for Hebb's postulate of learning. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[59]  W. Levick,et al.  Sustained and transient neurones in the cat's retina and lateral geniculate nucleus , 1971, The Journal of physiology.

[60]  K. Sanderson,et al.  The projection of the visual field to the lateral geniculate and medial interlaminar nuclei in the cat , 1971, The Journal of comparative neurology.

[61]  G S Brindley,et al.  Nerve net models of plausible size that perform many simple learning tasks , 1969, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[62]  W. Burke,et al.  Disuse in the lateral geniculate nucleus of the cat , 1968, The Journal of physiology.

[63]  J. S. GRIFFITH,et al.  A Theory of the Nature of Memory , 1966, Nature.

[64]  R W Guillery,et al.  A study of Golgi preparations from the dorsal lateral geniculate nucleus of the adult cat , 1966, The Journal of comparative neurology.

[65]  H. Barlow,et al.  Change of organization in the receptive fields of the cat's retina during dark adaptation , 1957, The Journal of physiology.

[66]  William B. Levy,et al.  Synaptic modification, neuron selectivity, and nervous system organization , 1985 .

[67]  H. Wässle Chapter 4 Morphological types and central projections of ganglion cells in the cat retina , 1982 .

[68]  W. Singer,et al.  The effects of early visual experience on the cat's visual cortex and their possible explanation by Hebb synapses. , 1981, The Journal of physiology.

[69]  W. Harris Neural activity and development. , 1981, Annual review of physiology.

[70]  J. Movshon,et al.  Visual neural development. , 1981, Annual review of psychology.

[71]  M. Dubin,et al.  Development of receptive-field properties of retinal ganglion cells in kittens. , 1977, Journal of neurophysiology.

[72]  M. H. Evans Tetrodotoxin, saxitoxin, and related substances: their applications in neurobiology. , 1972, International review of neurobiology.