RT Journal Article
SR Electronic
T1 Subcortical Representation of Non-Fourier Image Features
JF The Journal of Neuroscience
JO J. Neurosci.
FD Society for Neuroscience
SP 1985
OP 1993
DO 10.1523/JNEUROSCI.3258-09.2010
VO 30
IS 6
A1 Ari Rosenberg
A1 T. Robert Husson
A1 Naoum P. Issa
YR 2010
UL http://www.jneurosci.org/content/30/6/1985.abstract
AB A fundamental goal of visual neuroscience is to identify the neural pathways representing different image features. It is widely argued that the early stages of these pathways represent linear features of the visual scene and that the nonlinearities necessary to represent complex visual patterns are introduced later in cortex. We tested this by comparing the responses of subcortical and cortical neurons to interference patterns constructed by summing sinusoidal gratings. Although a linear mechanism can detect the component gratings, a nonlinear mechanism is required to detect an interference pattern resulting from their sum. Consistent with in vitro retinal ganglion cell recordings, we found that interference patterns are represented subcortically by cat LGN Y-cells, but not X-cells. Linear and nonlinear tuning properties of LGN Y-cells were then characterized and compared quantitatively with those of cortical area 18 neurons responsive to interference patterns. This comparison revealed a high degree of similarity between the two neural populations, including the following: (1) the representation of similar spatial frequencies in both their linear and nonlinear responses, (2) comparable orientation selectivity for the high spatial frequency carrier of interference patterns, and (3) the same difference in their temporal frequency selectivity for drifting gratings versus the envelope of interference patterns. The present findings demonstrate that the nonlinear subcortical Y-cell pathway represents complex visual patterns and likely underlies cortical responses to interference patterns. We suggest that linear and nonlinear mechanisms important for encoding visual scenes emerge in parallel through distinct pathways originating at the retina.