Gregory C. DeAngelis

Receptive-field dynamics in the central visual pathways

Neurons in the central visual pathways process visual images within a localized region of space, and a restricted epoch of time. Although the receptive field (RF) of a visually responsive neuron is inherently a spatiotemporal entity, most studies have focused exclusively on spatial aspects of RF structure. Recently, however, the application of sophisticated RF-mapping techniques has enabled neurophysiologists to characterize RFs in the joint domain of space and time. Studies that use these techniques have revealed that neurons in the geniculostriate pathway exhibit striking RF dynamics. For a majority of cells, the spatial structure of the RF changes as a function of time; thus, these RFs can be characterized adequately only in the space-time domain. In this review, the spatiotemporal RF structure of neurons in the lateral geniculate nucleus and primary visual cortex is discussed.

Cortical area MT and the perception of stereoscopic depth

Stereopsis is the perception of depth based on small positional differences between images formed on the two retinae (known as binocular disparity). Neurons that respond selectively to binocular disparity were first described three decades ago,, and have since been observed in many visual areas of the primate brain, including V1, V2, V3, MT and MST. Although disparity-selective neurons are thought to form the neural substrate for stereopsis, the mere existence of disparity-selective neurons does not guarantee that they contribute to stereoscopic depth perception. Some disparity-selective neurons may play other roles, such as guiding vergence eye movements,. Thus, the roles of different visual areas in stereopsis remain poorly defined. Here we show that visual area MT is important in stereoscopic vision: electrical stimulation of clusters of disparity-selective MT neurons can bias perceptual judgements of depth, and the bias is predictable from the disparity preference of neurons at the stimulation site. These results show that behaviourally relevant signals concerning stereoscopic depth are present in MT.

Neuronal Mechanisms Underlying Stereopsis: How Do Simple Cells in the Visual Cortex Encode Binocular Disparity?

Binocular neurons in the visual cortex are thought to form the neural substrate for stereoscopic depth perception. How are the receptive fields of these binocular neurons organized to encode the retinal position disparities that arise from binocular parallax? The conventional notion is that the two receptive fields of a binocular neuron have identical shapes, but are spatially offset from the point of retinal correspondence (zero disparity). We consider an alternative disparity-encoding scheme, in which the two receptive fields may differ in shape (or phase), but are centered at corresponding retinal locations. Using a reverse-correlation technique to obtain detailed spatiotemporal receptive-field maps, we provide support for the latter scheme. Specifically, we show that receptive-field profiles for the left and right eyes are matched for cells that are tuned to horizontal orientations of image contours. However, for neurons tuned to vertical orientations, the left and right receptive fields are predominantly dissimilar in shape. These results show that the striate cortex possesses a specialized mechanism for processing vertical contours, which carry the horizontal–disparity information needed for stereopsis. Thus, in a major modification to the traditional notion of the neural basis of stereopsis, we propose that binocular simple cells encode horizontal disparities in terms of phase at multiple spatial scales. Implications of this scheme are discussed with respect to the size–disparity correlation observed in psychophysical studies.

Development of inhibitory mechanisms in the kitten's visual cortex.

The objective of this study was to evaluate the maturity of three inhibitory mechanisms (end-inhibition, side-inhibition, and cross-orientation inhibition) in the striate cortex of kittens at 4 weeks postnatal. To accomplish this, we made extracellular recordings from area 17 neurons while presenting visual stimuli consisting of sinusoidal luminance gratings or composites of gratings. We then compared data from kittens relating to various characteristics of each inhibitory mechanism with data from adults. We find that end-inhibition, side-inhibition, and cross-orientation inhibition are all present in kittens, and all show signs of maturity by 4 weeks postnatal. We conclude that the development of these inhibitory mechanisms occurs relatively early, and may coincide with the development of excitatory properties.