Complex cell receptive fields: evidence for a hierarchical mechanism

被引:19
|
作者
van Kleef, Joshua P.
Cloherty, Shaun L.
Ibbotson, Michael R. [1 ]
机构
[1] Australian Natl Univ, Res Sch Biol, Div Biomed Sci & Biochem, Canberra, ACT 2601, Australia
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2010年 / 588卷 / 18期
基金
澳大利亚国家健康与医学研究理事会;
关键词
LATERAL GENICULATE-NUCLEUS; RETINAL GANGLION-CELLS; CONTRAST GAIN-CONTROL; SPATIAL SUMMATION; SELECTIVE NEURONS; VISUAL-CORTEX; FREQUENCY; SENSITIVITY; V1; ADAPTATION;
D O I
10.1113/jphysiol.2010.191452
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Simple cells in the primary visual cortex have segregated ON and OFF subregions in their receptive fields, while complex cells have overlapping ON and OFF subregions. These two cell types form the extremes at each end of a continuum of receptive field types. Hubel and Wiesel in 1962 suggested a hierarchical scheme of processing whereby spatially offset simple cells drive complex cells. Simple and complex cells are often classified by their responses to moving sine wave gratings: simple cells have oscillatory responses while complex cells produce unmodulated responses. Here, using moving gratings as stimuli, we show that a significant number of cells that display low levels of response modulation at high contrasts demonstrate high levels of response modulation at low contrasts. Most often a drifting low contrast grating generates a large phasic response at the fundamental frequency of the grating (F-1) and a smaller but significant phasic response that is approximately 180 deg out-of-phase with the F-1 component. We present several models capable of capturing the effects of stimulus contrast on complex cell responses. The model that best reproduces our experimental results is a variation of the classical hierarchical model. In our model several spatially offset simple cells provide input to a complex cell, with each simple cell exhibiting a different contrast response function. At low contrasts only one of these simple cells is sufficiently excited to reveal its receptive field properties. As contrast is increased additional spatially offset simple cells with higher contrast thresholds add their responses to the overall spiking activity.
引用
收藏
页码:3457 / 3470
页数:14
相关论文
共 50 条
  • [1] Spatial structure of complex cell receptive fields measured with natural images
    Touryan, J
    Felsen, G
    Dan, Y
    [J]. NEURON, 2005, 45 (05) : 781 - 791
  • [2] Spatiotemporal structure of complex cell receptive fields and influence of GABAergic inhibition
    Liu, Sheng
    Liu, Yong-Jun
    Li, Bing
    [J]. NEUROREPORT, 2007, 18 (15) : 1577 - 1581
  • [3] Hierarchical self-organization of minicolumnar receptive fields
    Lücke, J
    [J]. NEURAL NETWORKS, 2004, 17 (8-9) : 1377 - 1389
  • [4] Complex receptive fields in primary visual cortex
    Martinez, LM
    Alonso, JM
    [J]. NEUROSCIENTIST, 2003, 9 (05): : 317 - 331
  • [5] MECHANISM OF DIRECTIONAL SELECTIVITY OF NEURONS WITH COMPLEX RECEPTIVE-FIELDS IN THE CAT VISUAL-CORTEX
    STABINITE, DJ
    ALEKSEENKO, SV
    KIRVELIS, DJ
    [J]. NEUROPHYSIOLOGY, 1984, 16 (04) : 401 - 407
  • [6] Linear time-varying receptive fields explain complex-cell behaviour
    Garcia-Perez, MA
    [J]. PERCEPTION, 1998, 27 (02) : 242 - 243
  • [7] The complex structure of receptive fields in the middle temporal area
    Richert, Micah
    Albright, Thomas D.
    Krekelberg, Bart
    [J]. FRONTIERS IN SYSTEMS NEUROSCIENCE, 2013, 7
  • [8] Evidence for the intrinsically nonlinear nature of receptive fields in vision
    Marcelo Bertalmío
    Alex Gomez-Villa
    Adrián Martín
    Javier Vazquez-Corral
    David Kane
    Jesús Malo
    [J]. Scientific Reports, 10
  • [9] Evidence for the intrinsically nonlinear nature of receptive fields in vision
    Bertalmio, Marcelo
    Gomez-Villa, Alex
    Martin, Adrian
    Vazquez-Corral, Javier
    Kane, David
    Malo, Jesus
    [J]. SCIENTIFIC REPORTS, 2020, 10 (01)
  • [10] Modulating the dynamics of the horizontal cell receptive fields
    Kamermans, M
    Haak, J
    Verweij, J
    [J]. PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1996, 65 : PG208 - PG208