Visual processing shows a highly distributed organization in which the presentation of a visual stimulus simultaneously activates neurons in multiple columns across several cortical areas. It has been suggested that precise spatiotemporal activity patterns within and across cortical areas play a key role in higher cognitive, motor, and visual functions. In the visual system, these patterns have been proposed to take part in binding stimulus features into a coherent object, i.e., to be involved in perceptual grouping. Using voltagesensitive dye imaging (VSDI) in behaving monkeys (Macaca fascicularis, males), we simultaneously measured neural population activity in the primary visual cortex (V1) and extrastriate cortex (V2, V4) at high spatial and temporal resolution. We detected time point population events (PEs) in the VSDI signal of each pixel and found that they reflect transient increased neural activation within local populations by establishing their relation to spiking and local field potential activity. Then, we searched for repeating space and time relations between the detected PEs. We demonstrate the following: (1) spatiotemporal patterns occurring within (horizontal) and across (vertical) early visual areas repeat significantly above chance level; (2) information carried in only a few patterns can be used to reliably discriminate between stimulus categories on a single-trial level; (3) the spatiotemporal patterns yielding high classification performance are characterized by late temporal occurrence and top-down propagation, which are consistent with cortical mechanisms involving perceptual grouping. The pattern characteristics and the robust relation between the patterns and the stimulus categories suggest that spatiotemporal activity patterns play an important role in cortical mechanisms of higher visual processing.

The neuronal mechanisms underlying perceptual grouping of discrete, similarly oriented elements are not well understood. To investigate this, we measured neural population responses using voltage-sensitive dye imaging in V1 of monkeys trained on a contour-detection task. By mapping the contour and background elements onto V1, we could study their neural processing. Population response early in time showed activation patches corresponding to the contour/background individual elements. However, late increased activity in the contour elements, along with suppressed activity in the background elements, enabled us to visualize in single trials a salient continuous contour "popping out" from a suppressed background. This modulated activity in the contour and in background extended beyond the cortical representation of individual contour or background elements. Finally, the late modulation was correlated with behavioral performance of contour saliency and the monkeys' perceptual report. Thus, opposing responses in the contour and background may underlie perceptual grouping in V1.

Collinear proximal flankers can facilitate the detection of a low-contrast target or generate false-alarm target detection in the absence of a target. Although these effects are known to involve subthreshold neuronal interactions beyond the classical receptive field, the underlying neuronal mechanisms are not fully understood. Here, we used voltage-sensitive dye imaging that emphasizes subthreshold population activity, at high spatial and temporal resolution and imaged the visual cortex of fixating monkeys while they were presented with a low-contrast Gabor target, embedded within collinear or orthogonal flankers. We found that neuronal activity at the target site in area primary visual cortex increased and response latency decreased due to spatial spread of activation from the flankers' site. This increased activity was smaller than expected by a linear summation. The presentation of flankers alone induced strong spatial filling-in at the target site. Importantly, the increased neuronal activity at the target site was synchronized over time, both locally and with neuronal population at the flanker's site. This onset synchronization was higher for collinear than for orthogonal flankers. We further show that synchrony is a superior code over amplitude, for discriminating collinear from orthogonal pattern. These results suggest that population synchrony can serve as a code to discriminate contextual effects.

Gene alterations in pouch inflammation and CD overlap, suggesting that inflammatory bowel diseases is a spectrum, rather than distinct diseases. Pouchitis may serve as a model of CD. The novel pathways associated with inflammatory bowel diseases may decipher pathophysiology and suggest targets for intervention.

No abstract