Temporal properties of inputs to direction-selective neurons in monkey V1

Journal of Neurophysiology

Volumn 94, Issue 1, 2005, Pages 282-294

  Saul, Alan B ^a,b   Carras, Peter L ^a   Humphrey, Allen L ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b MEDICAL COLLEGE OF GEORGIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; DIRECTION SELECTIVE NERVE CELL; LATERAL GENICULATE NUCLEUS; MAGNOCELLULAR NUCLEUS; MONKEY; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; RECEPTIVE FIELD; SPATIAL ORIENTATION; TIME; VISUAL CORTEX; VISUAL NERVOUS SYSTEM;

ACTION POTENTIALS; ANIMALS; MACACA NEMESTRINA; MOTION PERCEPTION; NEURONS; ORIENTATION; PHOTIC STIMULATION; REACTION TIME; SPACE PERCEPTION; TIME FACTORS; VISUAL CORTEX; VISUAL FIELDS; VISUAL PATHWAYS;

EID: 21544451976     PISSN: 00223077     EISSN: None     Source Type: Journal    
DOI: 10.1152/jn.00868.2004     Document Type: Article

References (64)

1. Albrecht DG and Geisler WS. Motion selectivity and the contrast-response function of simple cells in the visual cortex. Vis Neurosci 7: 531-546, 1991.
2. Alonso J-M, Usrey WM, and Reid RC. Rules of connectivity between geniculate cells and simple cells in cat primary visual cortex. J Neurosci 21: 4002-4015, 2001.
3. Bauer U, Scholz M, Levitt JB, Obermayer K, and Lund JS. A model for the depth-dependence of receptive field size and contrast sensitivity of cells in layer 4C of macaque striate cortex. Vision Res 39: 613-629, 1999.
4. Blakemore C and Vital-Durand F. Organization and post-natal development of the monkey's lateral geniculate nucleus. J Physiol 380: 453-491, 1986.
5. Blasdel GG and Fitzpatrick D. Physiological organization of layer 4 in macaque striate cortex. J Neurosci 4: 880-895, 1984.
6. Blasdel GG and Lund JS. Termination of afferent axons in macaque striate cortex. J Neurosci 3: 1389-1413, 1983.
7. Boyd JD, Mavity-Hudson JA, and Casagrande VA. The connections of layer 4 subdivisions in the primary visual cortex (V1) of the owl monkey. Cereb Cortex 10: 644-662, 2000.
8. Cai D, DeAngelis GD, and Freeman RD. Spatiotemporal receptive field organization in the lateral geniculate nucleus of cats and kittens. J Neurophysiol 78: 1045-1061, 1997.
9. Chance FS, Nelson SB, and Abbott LF. Synaptic depression and the temporal response characteristics of V1 cells. J Neurosci 18: 4785-4799, 1998.
10. Conway BR and Livingstone MS. Space-time maps and two-bar interactions of different classes of direction-selective cells in macaque V-1. J Neurophysiol 89: 2726-2742, 2003.
11. Dean AF and Tolhurst DJ. Factors influencing the temporal phase of response to bar and grating stimuli for simple cells in the cat striate cortex. Exp Brain Res 62: 143-151, 1986.
12. DeAngelis GC, Ohzawa I, and Freeman RD. Spatiotemporal organization of simple-cell receptive fields in the cat's striate cortex. II. Linearity of temporal and spatial summation. J Neurophysiol 69: 1118-1135, 1993.
13. Derrington AM and Lennie P. Spatial and temporal contrast sensitivities of neurons in lateral geniculate nucleus of macaque. J Physiol 357: 219-240, 1984.
14. DeValois RL, Cottaris NP, Mahon LE, Elfar SD, and Wilson JA. Spatial and temporal receptive fields of geniculate and cortical cells and directional selectivity. Vision Res 40: 3685-3702, 2000.
15. Dreher B, Fukada Y, and Rodieck RW. Identification, classification and anatomical segregation of cells with X-like and Y-like properties in the lateral geniculate nucleus of Old World primates. J Physiol 258: 433-452, 1976.
16. Gur M, Kagan I, and Snodderly DM. Orientation and direction selectivity of neurons in V1 of alert monkeys: functional relationships and laminar distributions. Cereb Cortex 2004.
17. Hawken MJ and Parker AJ. Contrast sensitivity and orientation selectivity in lamina IV of the striate cortex of Old World monkeys. Exp Brain Res 54: 367-372, 1984.
18. Hendrickson AE, Wilson JR, and Ogren MP. The neuroanatomical organizations of pathways between dorsal lateral geniculate nucleus and visual cortex in Old and New World primates. J Comp Neurol 182: 123-136, 1978.
19. Hubel DH and Livingstone MS. Color and contrast sensitivity in the lateral geniculate body and primary visual cortex of the macaque monkey. J Neurosci 10: 2223-2237, 1990.
20. Hubel DH and Wiesel TN. Laminar and columnar distribution of geniculocortical fibers in macaque monkey. J Comp Neurol 146: 421-450, 1972.
21. Humphrey AL and Saul AB. The emergence of direction selectivity in cat primary visual cortex. In: The Cat Primary Visual Cortex, edited by Payne BR and Peters A. San Diego, CA: Academic, 2002, p. 343-386.
22. Jagadeesh B, Wheat HS, Kontsevitch LL, Tyler CW, and Ferster D. Direction selectivity of synaptic potentials in simple cells of the cat visual cortex. J Neurophysiol 78: 2772-2789, 1997.
23. Kagan I, Gur M, and Snodderly DM. Spatial organization of receptive fields of V1 neurons of alert monkeys: comparison with responses to gratings. J Neurophysiol 88: 2557-2574, 2002.
24. Kaplan E and Shapley RM. X and Y cells in the lateral geniculate nucleus of the macaque monkey. J Physiol 330: 125-143, 1982.
25. Kontsevich LL. The nature of inputs to cortical motion detectors. Vision Res 35: 2785-2793, 1995.
26. Lee BB, Pokorny J, Smith VC, and Kremers J. Responses to pulses and sinusoids in Macaque ganglion cells. Vision Res 34: 3081-3096, 1994.
27. Levitt JB, Schumer RA, Sherman SM, Spear PD, and Movshon JA. Visual response properties of neurons in the LGN of normally reared and visually deprived macaque monkeys. J Neurophysiol 85: 2111-2129, 2001.
28. Liu S and Wong-Riley M. Quantitative light- and electron-microscopic analysis of cytochome-oxidase distribution in neurons of the lateral geniculate nucleus of the adult monkey. Vis Neurosci 4: 969-987, 1990.
29. Livingstone MS. Mechanisms of direction selectivity in macaque V1. Neuron 20: 509-526, 1998.
30. Livingstone M and Hubel D. Segregation of form, color, movement and depth: anatomy, physiology, and perception, Science 240: 740-749, 1988.
31. Lund JS, Angelucci A, and Bressloff PC. Anatomical substrates for functional columns in macaque monkey primary visual cortex. Cereb Cortex 12: 15-24, 2003.
32. Martinez LM, Wang Q, Reid RC, Pillai C, Alonso J-M, Sommer FT, and Hirsch JA. Receptive field structure varies with layer in the primary visual cortex. Nat Neurosci 10.1038/nn1404, 2005.
33. Maex R and Orban GA. Model circuit of spiking neurons generating directional selectivity in simple cells. J Neurophysiol 75: 1515-1545, 1996.
34. Marrocco RT. Sustained and transient cells in monkey lateral geniculate nucleus: conduction velocites and response properties. J Neurophysiol 39: 340-353, 1976.
35. Mastronarde DN. 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: 381-413, 1987.
36. Maunsell JHR and Gibson JR. Visual response latencies in striate cortex of the macaque monkey. J Neurophysiol 68: 1332-1344, 1992.
37. McLean J and Palmer LA. Contribution of linear spatiotemporal receptive field structure to velocity selectivity of simple cells in area 17 of cat. Vision Res 29: 675-679, 1989.
38. McLean J, Raab S, and Palmer LA. Contribution of linear mechanisms to the specification of local motion by simple cells in areas 17 and 18 of the cat. Vis Neurosci 11: 271-294, 1994.
39. Movshon JA, Thompson ID, and Tolhurst DJ. Spatial summation in the receptive fields of simple cells in the cat's striate cortex. J Physiol 283: 53-77, 1978.
40. Murthy A, Humphrey AL, Saul AB, and Feidler JC. Laminar differences in the spatiotemporal structure of simple cell receptive fields in cat area 17. Vis Neurosci 15: 239-256, 1998.
41. Nassi JJ and Callaway EM. Contributions of magnocellular and parvocellular pathways to neurons in monkey primary visual cortex that provide direct versus indirect input to area MT. Soc Neurosci Abstr 30: 300.16, 2004.
42. Norden JJ and Kaas JH. The identification of relay neurons in the dorsal lateral geniculate nucleus of monkeys using horseradish peroxidase. J Comp Neurol 182: 707-726, 1978.
43. Nowak LG, Munk MH, Girard P, and Bullier J. Visual latencies in areas V1 and V2 of the macaque monkey. Vis Neurosci 12: 371-384, 1995.
44. Peterson MR, Li B, and Freeman RD. The derivation of direction selectivity in the striate cortex. J Neurosci 24: 3583-3591, 2004.
45. Priebe NJ and Ferster D. Direction selectivity of excitation and inhibition in simple cells of the cat primary visual cortex. Neuron 45: 133-145, 2005.
46. Reid RC, Alonso J-M, and Usrey WM. Integration of thalamic inputs to cat primary visual cortex. In: The Cat Primary Visual Cortex, edited by Payne BR and Peters A. San Diego, CA: Academic, 2002, p. 319-342.
47. Reid RC, Soodak RE, and Shapley RM. Linear mechanisms of directional selectivity in simple cells of cat striate cortex. Proc Natl Acad Sci USA 84: 8740-8744, 1987.
48. Saul AB. Adaptation aftereffects in single neurons of cat visual cortex: response timing is retarded by adapting. Visual Neurosci 12: 191-205, 1995.
49. Saul AB. Visual cortical simple cells: who inhibits whom. Visual Neurosci 16: 667-673, 1999.
50. Saul AB. Turn, turn, turn. It's not too late! Temporal processing is better measured in terms of phase rather than latency. Soc Neurosci Abstr 30: 410.6, 2004.
51. Saul AB, Carras PL, and Humphrey AL. Sources of response timing to direction selective cells in macaque striate cortex. Soc Neurosci Abstr 27: 164.9, 2001.
52. Saul AB and Humphrey AL. Spatial and temporal response properties of lagged and nonlagged cells in cat lateral geniculate nucleus. J Neurophysiol 64: 206-224, 1990.
53. Saul AB and Humphrey AL. Temporal frequency tuning of direction selectivity in cat visual cortex. Vis Neurosci 8: 365-372, 1992a.
54. Saul AB and Humphrey AL. Evidence of input from lagged cells in the lateral geniculate nucleus to simple cells in cortical area 17 of the cat. J Neurophysiol 68: 1190-1208, 1992b.
55. Sawatari A and Callaway EM. Convergence of magno- and parvocellular pathways in layer 4B of macaque primary visual cortex. Nature 380: 442-446, 1996.
56. Schiller PH and Malpeli JG. Functional specificity of lateral geniculate nucleus laminae of the rhesus monkey. J Neurophysiol 41: 788-797, 1978.
57. Schmolesky MT, Wang Y, Hanes DP, Thompson KG, Leutgeb S, Schall JD, and Leventhal AG. Signal timing across the macaque visual system. J Neurophysiol 79: 3272-3278, 1998.
58. Shapley R, Hawken M, and Ringach DL. Dynamics of orientation selectivity in the primary visual cortex and the importance of cortical inhibition. Neuron 38: 689-699, 2003.
59. Sherman SM, Wilson JR, Kaas JH, and Webb SV. X- and Y-cells in the dorsal lateral geniculate nucleus of the owl monkey (Aotus trivirgatus). Science 192: 475-477, 1976.
60. Spear PD, Moore RJ, Kim CB, Xue JT, and Tumosa N. Effects of aging on the primate visual system: spatial and temporal processing by lateral geniculate neurons in young adult and old rhesus monkeys. J Neurophysiol 72: 402-420, 1994.
61. Suarez H, Koch C, and Douglas R. Modeling direction selectivity of simple cells in striate visual cortex within the framework of the canonical microcircuit. J Neurosci 15: 6700-6719, 1995.
62. Tooted RBH, Hamilton SL, and Switkes E. Functional anatomy of macaque striate cortex. IV. Contrast and magno-parvo streams. J Neurosci 8: 1594-1609, 1988.
63. Usrey WM and Reid RC. Visual physiology of the lateral geniculate nucleus in two species of new world monkey: Saimiri sciureus and Aotus trivirgatis. J Physiol 15: 755-769, 2000.
64. Yabuta NH, Sawatari A, and Callaway EM. Two functional channels from primary visual cortex to dorsal visual cortical areas. Science 292: 297-300, 2001.