Membrane properties of morphologically identified X and Y cells in the lateral geniculate nucleus of the cat in vitro.

1. The membrane properties and the electrotonic features of cells in lamina A of the cat dorsal lateral geniculate nucleus (l.g.n.) were studied using an in vitro slice preparation. 2. Following intrasomatic injection of horseradish peroxidase (HRP) each neurone was classified as an X (n = 20) or a Y (n = 27) cell on the basis of its morphology. For both classes, the frequency distribution of soma area was similar to that reported in vivo where the identification of X and Y cells in lamina A of the cat l.g.n. was based on physiological criteria. 3. No difference was observed in the mean resting membrane potential between the two classes of cells. However, the input resistance (RN) of X cells was greater (82 M omega) and their membrane time constant (tau 0) longer (22 ms) than of Y cells (RN, 32 M omega; tau 0, 15 ms). 4. Using a simple neuronal model, the calculated electrotonic length (L) and the dendritic to somatic conductance ratio (rho) were similar for the two classes of cells. The mean value of L (0.7) and rho (1.9) suggests that both X and Y cells are electrically compact. 5. The specific membrane resistance (Rm, 28,000 omega cm2) of X cells, calculated using two different approaches, was found to be higher than that of Y cells (17,000 omega cm2). 6. The implication of these results for the integration of synaptic signals in the two classes of l.g.n. cells and the feasibility of differentiating between X and Y cells on the basis of their membrane properties are discussed.

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

[2]  P. Schwindt,et al.  Cable properties of layer V neurons from cat sensorimotor cortex in vitro. , 1984, Journal of neurophysiology.

[3]  V. Crunelli,et al.  An in vitro slice preparation of the cat lateral geniculate nucleus , 1987, Journal of Neuroscience Methods.

[4]  D Ferster,et al.  Relay cell classes in the lateral geniculate nucleus of the cat and the effects of visual deprivation , 1977, The Journal of comparative neurology.

[5]  V. Crunelli,et al.  X- and Y-cells identified in the cat lateral geniculate nucleus in vitro , 1986, Brain Research.

[6]  B. L. Ginsborg THE PHYSIOLOGY OF SYNAPSES , 1964 .

[7]  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.

[8]  A. G. Brown,et al.  Intracellular staining of mammalian neurones , 1984 .

[9]  J. Eccles The Physiology of Synapses , 1964, Springer Berlin Heidelberg.

[10]  S. Sato,et al.  Some properties of the theoretical membrane transients in Rall's neuron model. , 1976, Journal of theoretical biology.

[11]  M. Deschenes,et al.  Electrophysiology of neurons of lateral thalamic nuclei in cat: resting properties and burst discharges. , 1984, Journal of neurophysiology.

[12]  V. Crunelli,et al.  Blockade of amino acid‐induced depolarizations and inhibition of excitatory post‐synaptic potentials in rat dentate gyrus. , 1983, The Journal of physiology.

[13]  R. Llinás,et al.  Electrophysiological properties of guinea‐pig thalamic neurones: an in vitro study. , 1984, The Journal of physiology.

[14]  R. Llinás,et al.  Hippocampal pyramidal cells: significance of dendritic ionic conductances for neuronal function and epileptogenesis. , 1979, Journal of neurophysiology.

[15]  M. Pirchio,et al.  The ventral and dorsal lateral geniculate nucleus of the rat: intracellular recordings in vitro. , 1987, The Journal of physiology.

[16]  T. H. Brown,et al.  Passive electrical constants in three classes of hippocampal neurons. , 1981, Journal of neurophysiology.

[17]  W Singer,et al.  Control of thalamic transmission by corticofugal and ascending reticular pathways in the visual system. , 1977, Physiological reviews.

[18]  T. H. Brown,et al.  Electrotonic structure and specific membrane properties of mouse dorsal root ganglion neurons. , 1981, Journal of neurophysiology.

[19]  W. Burke,et al.  Extraretinal influences on the lateral geniculate nucleus. , 1978, Reviews of physiology, biochemistry and pharmacology.

[20]  C. Nicholson Electric current flow in excitable cells J. J. B. Jack, D. Noble &R. W. Tsien Clarendon Press, Oxford (1975). 502 pp., £18.00 , 1976, Neuroscience.

[21]  M. L. Schmidt,et al.  A quantitiative study of the occurrence and distribution of cytoplasmic laminated bodies in the lateral geniculate nucleus of the normal adult cat , 1980, The Journal of comparative neurology.

[22]  J. Bullier,et al.  X and Y relay cells in cat lateral geniculate nucleus: quantitative analysis of receptive-field properties and classification. , 1979, Journal of neurophysiology.

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

[24]  C. Koch,et al.  Understanding the intrinsic circuitry of the cat’s lateral geniculate nucleus: electrical properties of the spine-triad arrangement , 1985, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[25]  Y. Burnod,et al.  Dorsolateral geniculate neurons in vitro: Reduced postsynaptic excitability following repetitive activation of the optic tract , 1985, Neuroscience Letters.

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

[27]  R. Llinás,et al.  Ionic basis for the electro‐responsiveness and oscillatory properties of guinea‐pig thalamic neurones in vitro. , 1984, The Journal of physiology.

[28]  H. Haas,et al.  A simple perfusion chamber for the study of nervous tissue slices in vitro , 1979, Journal of Neuroscience Methods.

[29]  ROBERT SHAPLEY,et al.  Visual spatial summation in two classes of geniculate cells , 1975, Nature.