Origin and Dynamics of Extraclassical Suppression in the Lateral Geniculate Nucleus of the Macaque Monkey

Neuron

Volumn 57, Issue 1, 2008, Pages 135-146

  Alitto, Henry J ^a,b   Usrey, W Martin ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

SYSNEURO

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; LATERAL GENICULATE NUCLEUS; MACACA; MAGNOCELLULAR NUCLEUS; NEGATIVE FEEDBACK; NERVE CELL; NONHUMAN; PARVOCELLULAR NERVE CELL; POSITIVE FEEDBACK; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RETINA; STIMULUS RESPONSE; VISUAL STIMULATION;

ACTION POTENTIALS; ANESTHESIA; ANIMALS; CONTRAST SENSITIVITY; FEEDBACK; GENICULATE BODIES; MACACA MULATTA; MODELS, BIOLOGICAL; NEURAL INHIBITION; NEURONS; NONLINEAR DYNAMICS; NORMAL DISTRIBUTION; PHOTIC STIMULATION; REACTION TIME; SPACE PERCEPTION; VISUAL PATHWAYS; WAKEFULNESS;

EID: 37549053286     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuron.2007.11.019     Document Type: Article

References (65)

1. Albrecht D.G., and Hamilton D.B. Striate cortex of monkey and cat: contrast response function. J. Neurophysiol. 48 (1982) 217-237
2. Alonso J.-M., Usrey W.M., and Reid R.C. Rules of connection for neurons in the lateral geniculate nucleus and visual cortex. J. Neurosci. 21 (2001) 4002-4015
3. Angelucci A., and Bressloff P.C. Contribution of feedforward, lateral and feedback connections to the classical receptive field center and extra-classical receptive field surround of primate V1 neurons. Prog. Brain Res. 154 (2006) 93-120
4. Angelucci A., and Sainsbury K. Contribution of feedforward thalamic afferents and corticogeniculate feedback to the spatial summation area of macaque V1 and LGN. J. Comp. Neurol. 498 (2006) 330-351
5. Bair W., Cavanaugh J.R., and Movshon J.A. Time course and time-distance relationships for surround suppression in macaque V1 neurons. J. Neurosci. 23 (2003) 7690-7701
6. Benardete E.A., and Kaplan E. The dynamics of primate M retinal ganglion cells. Vis. Neurosci. 16 (1999) 355-368
7. Benardete E.A., Kaplan E., and Knight B.W. Contrast gain control in the primate retina: P cells are not X-like, some M cells are. Vis. Neurosci. 8 (1992) 483-486
8. Bonin V., Mante V., and Carandini M. The suppressive field of neurons in lateral geniculate nucleus. J. Neurosci. 25 (2005) 10844-10856
9. Bourassa J., and Deschenes M. Corticothalamic projections from the primary visual cortex in rats: a single fiber study using biocytin as an anterograde tracer. Neuroscience 66 (1995) 253-263
10. Briggs F., and Usrey W.M. Temporal properties of feedforward and feedback pathways between the thalamus and visual cortex in the ferret. Thalamus and Related Systems 3 (2005) 133-139
11. Briggs F., and Usrey W.M. A fast, reciprocal pathway between the lateral geniculate nucleus and visual cortex in the macaque monkey. J. Neurosci. 27 (2007) 5431-5436
12. Cavanaugh J.R., Bair W., and Movshon J.A. Nature and interaction of signals from the receptive field center and surround in macaque V1 neurons. J. Neurophysiol. 88 (2002) 2530-2546
13. Cavanaugh J.R., Bair W., and Movshon J.A. Selectivity and spatial distribution of signals from the receptive field surround in macaque V1 neurons. J. Neurophysiol. 88 (2002) 2547-2556
14. Cudeiro J., and Sillito A.M. Spatial frequency tuning of orientation-discontinuity-sensitive corticofugal feedback to the cat lateral geniculate nucleus. J. Physiol. 490 (1996) 481-492
15. Dobbins A., Zucker S.W., and Cynader M.S. Endstopped neurons in the visual cortex as a substrate for calculating curvature. Nature 329 (1987) 438-441
16. Erisir A., Van Horn S.C., and Sherman S.M. Relative numbers of cortical and brainstem inputs to the lateral geniculate nucleus. Proc. Natl. Acad. Sci. USA 94 (1997) 1517-1520
17. Erisir A., Van Horn S.C., and Sherman S.M. Distribution of synapses in the lateral geniculate nucleus of the cat: differences between laminae A and A1 and between relay cells and interneurons. J. Comp. Neurol. 390 (1998) 247-255
18. Felisberti F., and Derrington A.M. Long-range interactions modulate the contrast gain in the lateral geniculate nucleus of cats. Vis. Neurosci. 16 (1999) 943-956
19. Fitzpatrick D. Seeing beyond the receptive field in primary visual cortex. Curr. Opin. Neurobiol. 10 (2000) 438-443
20. Funke K., and Eysel U.T. Inverse correlation of firing patterns of single topographically matched perigeniculate neurons and cat dorsal lateral geniculate relay cells. Vis. Neurosci. 15 (1998) 711-729
21. Girardin C.C., Kiper D.C., and Martin K.A. The effect of moving textures on the responses of cells in the cat's dorsal lateral geniculate nucleus. Eur. J. Neurosci. 16 (2002) 2149-2156
22. Grieve K.L., and Sillito A.M. Differential properties of cells in the feline primary visual cortex providing the corticofugal feedback to the lateral geniculate nucleus and visual claustrum. J. Neurosci. 15 (1995) 4868-4874
23. Guillery R.W. A quantitative study of synaptic interconnections in the dorsal lateral geniculate nucleus of the cat. Z. Zellforsch 96 (1969) 39-48
24. Hirsch J.A., Gallagher C.A., Alonso J.M., and Martinez L.M. Ascending projections of simple and complex cells in layer 6 of the cat striate cortex. J. Neurosci. 18 (1998) 8086-8094
25. Jones H.E., Andolina I.M., Oakely N.M., Murphy P.C., and Sillito A.M. Spatial summation in lateral geniculate nucleus and visual cortex. Exp. Brain Res. 135 (2000) 279-284
26. Jones H.E., Wang W., and Sillito A.M. Spatial organization and magnitude of orientation contrast interactions in primate V1. J. Neurophysiol. 88 (2002) 2796-2808
27. Kapadia M.K., Westheimer G., and Gilbert C.D. Dynamics of spatial summation in primary visual cortex of alert monkeys. Proc. Natl. Acad. Sci. USA 96 (1999) 12073-12078
28. Kaplan E., and Benardete E. The dynamics of primate retinal ganglion cells. Prog. Brain Res. 134 (2001) 17-34
29. Knierim J.J., and van Essen D.C. Neuronal responses to static texture patterns in area V1 of the alert macaque monkey. J. Neurophysiol. 67 (1992) 961-980
30. Kuffler S.W. Neurons in the retina; organization, inhibition and excitation problems. Cold Spring Harb. Symp. Quant. Biol. 17 (1952) 281-292
31. Lamme V.A. The neurophysiology of figure-ground segregation in primary visual cortex. J. Neurosci. 15 (1995) 1605-1615
32. Levick W.R., Cleland B.G., and Dubin M.W. Lateral geniculate neurons of cat: retinal inputs and physiology. Inv. Opthalm. 11 (1972) 302-311
33. Levine M.W., and Cleland B.G. An analysis of the effect of retinal ganglion cell impulses upon the firing probability of neurons in the dorsal lateral geniculate nucleus of the cat. Brain Res. 902 (2001) 244-254
34. Levitt J.B., and Lund J.S. Contrast dependence of contextual effects in primate visual cortex. Nature 387 (1997) 73-76
35. Levitt J.B., and Lund J.S. The spatial extent over which neurons in macaque striate cortex pool visual signals. Vis. Neurosci. 19 (2002) 439-452
36. Mastronarde D.N. Two classes of single-input X-cells in cat lateral geniculate nucleus. II. Retinal inputs and the generation of receptive-field properties. J. Neurophysiol. 57 (1987) 381-413
37. Montero V.M. A quantitative study of synaptic contacts on interneurons and relay cells of the cat lateral geniculate nucleus. Exp. Brain Res. 86 (1991) 257-270
38. Murphy P.C., and Sillito A.M. Corticofugal feedback influences the generation of length tuning in the visual pathway. Nature 329 (1987) 727-729
39. Murphy P.C., and Sillito A.M. Functional morphology of the feedback pathway from area 17 of the cat visual cortex to the lateral geniculate nucleus. J. Neurosci. 16 (1996) 1180-1192
40. Nolt M.J., Kumbhani R.D., and Palmer L.A. Contrast-dependent spatial summation in the lateral geniculate nucleus and retina of the cat. J. Neurophysiol. 92 (2004) 1708-1717
41. Nolt M.J., Kumbhani R.D., and Palmer L.A. Suppression at high spatial frequencies in the lateral geniculate nucleus of the cat. J. Neurophysiol. 98 (2007) 1167-1180
42. Przybyszewski A.W., Gaska J.P., Foote W., and Pollen D.A. Striate cortex increases contrast gain of macaque LGN neurons. Vis. Neurosci. 17 (2000) 485-494
43. Rowe M.H., and Fischer Q. Dynamic properties of retino-geniculate synapses in the cat. Vis. Neurosci. 18 (2001) 219-231
44. Ruksenas O., Fjeld I.T., and Heggelund P. Spatial summation and center-surround antagonism in the receptive field of single units in the dorsal lateral geniculate nucleus of cat: comparison with retinal input. Vis. Neurosci. 17 (2000) 855-870
45. Sceniak M.P., Ringach D.L., Hawken M.J., and Shapley R. Contrast's effect on spatial summation by macaque V1 neurons. Nat. Neurosci. 2 (1999) 733-739
46. Sceniak M.P., Hawken M.J., and Shapley R. Visual spatial characterization of macaque V1 neurons. J. Neurophysiol. 85 (2001) 1873-1887
47. Sceniak M.P., Chatterjee S., and Callaway E.M. Visual spatial summation in macaque geniculocortical afferents. J. Neurophysiol. 96 (2006) 3474-3484
48. Shapley R.M., and Victor J.D. The effect of contrast on the transfer properties of cat retinal ganglion cells. J. Physiol. 285 (1978) 275-298
49. Shapley R.M., and Victor J.D. How the contrast gain control modifies the frequency responses of cat retinal ganglion cells. J. Physiol. 318 (1981) 161-179
50. Sillito A.M., and Jones H.E. Corticothalamic interactions in the transfer of visual information. Philos. Trans. R. Soc. Lond. B Biol. Sci. 357 (2002) 1739-1752
51. Sillito A.M., Grieve K.L., Jones H.E., Cudeiro J., and Davis J. Visual cortical mechanisms detecting focal orientation discontinuities. Nature 378 (1995) 492-496
52. Sincich L.C., Adams D.L., Economides J.R., and Horton J.C. Transmission of spike trains at the retinogeniculate synapse. J. Neurosci. 27 (2007) 2683-2692
53. Smith M.A., Bair W., and Movshon J.A. Dynamics of suppression in macaque primary visual cortex. J. Neurosci. 26 (2006) 4826-4834
54. Solomon S.G., White A.J., and Martin P.R. Extraclassical receptive field properties of parvocellular, magnocellular, and koniocellular cells in the primate lateral geniculate nucleus. J. Neurosci. 22 (2002) 338-349
55. Solomon S.G., Lee B.B., and Sun H. Suppressive surrounds and contrast gain in magnocellular-pathway retinal ganglion cells of macaque. J. Neurosci. 26 (2006) 8715-8726
56. Tsumoto T., and Suda K. Three groups of cortico-geniculate neurons and their distribution in binocular and monocular segments of cat striate cortex. J. Comp. Neurol. 193 (1980) 223-236
57. Usrey W.M., and Reid R.C. Synchronous activity in the visual system. Annu. Rev. Physiol. 61 (1999) 435-456
58. Usrey W.M., Reppas J.B., and Reid R.C. Paired-spike interactions and synaptic efficacy of retinal inputs to thalamus. Nature 395 (1998) 384-387
59. Usrey W.M., Alonso J.-M., and Reid R.C. Synaptic interactions between thalamic inputs to simple cells in cat visual cortex. J. Neurosci. 20 (2000) 5461-5467
60. Walker G.A., Ohzawa I., and Freeman R.D. Suppression outside the classical cortical receptive field. Vis. Neurosci. 17 (2000) 369-379
61. Webb B.S., Tinsley C.J., Barraclough N.E., Easton A., Parker A., and Derrington A.M. Feedback from V1 and inhibition from beyond the classical receptive field modulates the responses of neurons in the primate lateral geniculate nucleus. Vis. Neurosci. 19 (2002) 583-592
62. Webb B.S., Tinsley C.J., Vincent C.J., and Derrington A.M. Spatial distribution of suppressive signals outside the classical receptive field in lateral geniculate nucleus. J. Neurophysiol. 94 (2005) 1789-1797
63. Weber A.J., Kalil R.E., and Behan M. Synaptic connections between corticogeniculate axons and interneurons in the dorsal lateral geniculate nucleus of the cat. J. Comp. Neurol. 289 (1989) 156-164
64. Weyand T.G. Retinogeniculate transmission in wakefulness. J. Neurophysiol. 98 (2007) 769-785
65. Yeh T., Lee B.B., Kremers J., Cowing J.A., Hunt D.M., Martin P.R., and Troy J.B. Visual responses in the lateral geniculate nucleus of dichromatic and trichromatic marmosets (Callithrix jacchus). J. Neurosci. 15 (1995) 7892-7904