Neural correlates of motion-induced blindness in the human brain

Motion-induced blindness (MIB) is a visual phenomenon in which highly salient visual targets spontaneously disappear from visual awareness (and subsequently reappear) when superimposed on a moving background of distracters. Such fluctuations in awareness of the targets, although they remain physically present, provide an ideal paradigm to study the neural correlates of visual awareness. Existing behavioral data on MIB are consistent both with a role for structures early in visual processing and with involvement of high-level visual processes. To further investigate this issue, we used high field functional MRI to investigate signals in human low-level visual cortex and motion-sensitive area V5/MT while participants reported disappearance and reappearance of an MIB target. Surprisingly, perceptual invisibility of the target was coupled to an increase in activity in low-level visual cortex plus area V5/MT compared with when the target was visible. This increase was largest in retinotopic regions representing the target location. One possibility is that our findings result from an active process of completion of the field of distracters that acts locally in the visual cortex, coupled to a more global process that facilitates invisibility in general visual cortex. Our findings show that the earliest anatomical stages of human visual cortical processing are implicated in MIB, as with other forms of bistable perception

The influence of spontaneous activity on stimulus processing in primary visual cortex

Spontaneous activity in the resting human brain has been studied extensively; however, how such activity affects the local processing of a sensory stimulus is relatively unknown. Here, we examined the impact of spontaneous activity in primary visual cortex on neuronal and behavioural responses to a simple visual stimulus, using functional MRI. Stimulus-evoked responses remained essentially unchanged by spontaneous fluctuations, combining with them in a largely linear fashion (i.e., with little evidence for an interaction). However, interactions between spontaneous fluctuations and stimulus-evoked responses were evident behaviourally: high levels of spontaneous activity tended to be associated with increased stimulus detection at perceptual threshold. Our results extend those found in studies of spontaneous fluctuations in motor cortex and higher order visual areas, and suggest a fundamental role for spontaneous activity in stimulus processing. (C) 2011 Elsevier Inc. All rights reserved

The interplay between spontaneous and evoked brain activity during visual perception

The vast majority of studies in cognitive neuroscience have focused on the brain’s response to a task or stimulus. However, the brain is very active even in the absence of explicit input or output, as its enormous energy consumption at rest suggests. This ongoing brain activity is present at all timescales; as spontaneous neuronal firing measured by electrophysiology, and as slow fluctuations in the BOLD signal measured by functional magnetic resonance imaging (fMRI). Its significance for behaviour is still unclear. This thesis explores the nature of the brain’s spontaneous activity, with an emphasis on its interaction with brain activity devoted to visual perception. Using a theoretical approach, I first show that the amount of energy expended on evoked brain activity related to a perceptual decision is minute compared to the energy expenditure associated with spontaneous activity. I then focus on spontaneous brain activity measured in the fMRI signal, the so-called resting-state fluctuations. Using simultaneous fMRI-electrophysiology in awake monkeys, I demonstrate that these fMRI resting-state fluctuations are strongly correlated to underlying fluctuations in neural activity, and are therefore likely to be neural in origin. A further fMRI study in humans shows that resting-state fluctuations in visual cortex can account for a significant degree to the variability in cortical, and to a lesser degree to the variability in behavioural responses to a visual stimulus at perceptual threshold. Lastly, I use a visual illusion called motion-induced blindness as a model system for studying the effect of spontaneous fluctuations in internal brain state on bistable perception. Using fMRI in humans, I show that while the retinal input remains constant, activity in early visual cortex reflects awareness of the stimulus. In the final, behavioural experiments, I manipulate the brain’s internal state by examining the influence of endogenous attention on the temporal dynamics of motion-induced blindness. Taken together, these studies show that spontaneous brain activity plays an important role in visual perception, and argue that understanding the brain’s internal dynamics is essential to understanding the brain as a whole

Fluorescent Cell Barcoding as a Tool to Assess the Age-Related Development of Intracellular Cytokine Production in Small Amounts of Blood from Infants

Fluorescent Cell Barcoding (FCB) is a flow cytometric technique which has been used for assessing signaling proteins. This FCB technique has the potential to be applied in other multiparameter analyses. Since data on antigen (Ag)-specific T-cell immune responses, like intracellular cytokine production, are still lacking in infants because limited blood volumes can be obtained for analysis, the FCB technique could be very useful for this purpose. The objectives of this study were to modify the FCB method to be able to measure multiple Ag-specific cytokine reponses in T-cells upon simultaneous stimulation by various antigens and mitogens in small amounts of blood and to investigate the cytokine pattern of T-cell subsets in healthy infants aged six and twelve months. Blood samples, collected from 20 healthy infants aged six and twelve months, were stimulated in vitro with the antigens: phorbol-myristate-acetate (PMA), purified-protein-derivative (PPD), Tetanus-toxoid (TT), Staphylococcal-enterotoxin-B (SEB), and phytohemagglutinin (PHA). Each stimulus was barcoded by labelling with different intensities of fluorescent cell barcoding (FCB) markers. Intracellular production of interleukin-2, interferon-gamma, and tumor necrosis factor-alpha was measured simultaneously in just one blood sample of 600 µl whole blood. Significant age-related differences in cytokine production were shown for PMA, PHA, and TT in CD4+ T-cells, and for PMA, PHA, SEB, and TT in CD8+ T-cells. The intracellular cytokine production by CD4+ and CD8+ T-cells was higher at twelve months compared to six months of age for all antigens, except for PMA, which was lower at the age of twelve months. Based on the consistency in both T-cell subsets, we conclude that the new FCB method is a promising tool to investigate the age-related development of intracellular cytokine production in infants