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Matuszewski, J.

Publications and source records attributed to Matuszewski, J..

3 recordsLinked to original sources

Early blindness shifts the feedforward laminar profile of hMT+/V5 from visual to auditory motion

The occipital cortex of people born blind massively enhances its response to sounds, but the brain circuitry supporting such crossmodal plasticity remains elusive. Here we capitalized on ultra-high-field fMRI (7T) coupled with sub-millimetre BOLD and VASO acquisitions to infer whether motion-related information is processed via feedforward or feedback pathways, probing responses to visual motion in sighted participants and auditory motion in both sighted and early blind individuals. By identifying circuitry from layer-dependent activity of the middle temporal cortex (hMT+/V5), we observed that moving, but not static, sounds selectively elicited a feedforward response in the middle layers of hMT+/V5 of blind people, analogous to visual motion processing in sighted individuals. Furthermore, we observed that hMT+/V5 shows enhanced auditory motion-selective connectivity with the Planum Temporale in the sighted and with the cuneus in blind people. These findings reveal that hMT+/V5 implements a feedforward motion selective response profile in sighted and blind individuals, with its sensory input shifting from vision to audition in the absence of visual experience.

neuroscience↗

Correlated and Anticorrelated Binocular Disparity Modulate GABA+ and Glutamate/glutamine Concentrations in the Human Visual Cortex

Binocular disparity is used for perception and action in three dimensions. Neurons in the primary visual cortex respond to binocular disparity in random dot patterns, even when the contrast is inverted between eyes (false depth cue). In contrast, neurons in the ventral stream largely cease to respond to false depth cues. This study evaluated whether GABAergic inhibition is involved in suppressing false depth cues in the human ventral visual cortex. We compared GABAergic inhibition (GABA+) and glutamatergic excitation (Glx) during the viewing of correlated and anticorrelated binocular disparity in 18 participants using single voxel proton magnetic-resonance spectroscopy (MRS). Measurements were taken from the early visual cortex (EVC) and the lateral occipital cortex (LO). Three visual conditions were presented per voxel location: correlated binocular disparity; anticorrelated binocular disparity; or a blank grey screen with a fixation cross. To identify differences in neurochemistry, GABA+ or Glx levels were compared across viewing conditions. In EVC, correlated disparity increased Glx over anticorrelated and rest conditions, also mirrored in the Glx/GABA+ ratio. In LO, anticorrelated disparity decreased GABA+ and increased Glx. Joint effects on GABA+ and Glx were summarised by the Glx/GABA+ ratio, which showed increased excitatory over inhibitory drive to anticorrelated disparity in LO. Glx during viewing of anticorrelation in LO was predictive of its object-selective BOLD-activity. We provide evidence that early and ventral visual cortices change GABA+ and Glx concentrations during presentation of correlated and anticorrelated disparity, suggesting a contribution of cortical excitation and inhibition in disparity selectivity. Significance StatementThe visual system must correctly match elements from the left and right eye for proper reconstruction of binocular depth. At the earliest part of binocular processing, false matches can activate depth detectors, however, the activation to false matches is absent in the ventral visual stream. We tested whether GABAergic inhibition contributes to the suppression of false matches in the ventral stream by measuring GABAergic inhibition and glutamatergic excitation in the human visual cortex during the presentation of correct and false matches. Correct matches increased excitation in response in the early visual cortex, and false matches increased excitation and decreased in the ventral visual cortex. These results suggest a role for excitation and inhibition in distinguishing depth cues for stereoscopic vision.

neuroscience↗

Widespread neural reorganization related to expertise in reading visual Braille

Learning to read assigns linguistic value to an abstract visual code. Whether regions of the reading network tune to visual properties common to most scripts or code for more abstracted units of language remains debated. Here we investigate this question using visual Braille, a script developed for touch that does not share the typical explicit shape information of other alphabets, yet maps onto the same phonology and lexicon as other more regular scripts. First, we compared univariate responses in visual Braille readers and a naive control group and found that individually localized Visual Word Form Area (VWFA) was selectively activated for visual Braille when compared to scrambled Braille only in expert Braille readers. Multivariate analyses showed that linguistic properties can be decoded from Latin script in both groups and from Braille script in expert readers in an extended network of brain regions including the early visual cortex (V1), the lateral occipital region (LO), the VWFA and the left Posterior Temporal area (l-PosTemp). These results suggest that the tuning of an extended reading network to orthography relies more on the linguistic content of the script rather than their specific visual features (e.g. line junctions). Nevertheless, cross-scripts generalization was significantly lower than within-script decoding and failed to reveal common representations across Latin and Braille in experts in all regions except the l-PosTemp. These results suggest that V1, LO and VWFA encode orthographic representations in a script-specific manner, whereas l-PosTemp encodes abstracted linguistic information.

neuroscience↗