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Roy, T. S.

Publications and source records attributed to Roy, T. S..

2 recordsLinked to original sources

A transformation from vision to imagery in the human brain

Extensive work has shown that the visual cortex is reactivated during mental imagery, and that models trained on visual data can predict imagery activity and decode imagined stimuli. These findings may explain why imagery can feel and function like vision, but give little insight into how the brain activity patterns that encode seen and mental images differ. While one popular theory ("weak vision") suggests that imagery differs from vision only in strength, recent work points to more complex differences. To clarify the relationship between visual and imagery activity in the human brain, we introduce the concept of an imagery transformation--a mapping from visual to imagery activity patterns evoked by the same stimulus. Importantly, this approach can describe a variety of possible scenarios, from simple rescaling to the selective removal or reorientation of activity dimensions. Using two 7T fMRI datasets, we estimated imagery transformations across different visual areas and found they accurately predict imagery activity. We show that imagery transformations are indeed more complex than simple weakening: in early visual cortex, they halve the number of active dimensions and reorient them, such that reconstructions of visual activity in terms of imagery dimensions explain only 25-50% of the variance. Nonetheless, these reoriented dimensions still coarsely encode the features encoded by the principal dimensions of visual activity. These findings help to explain the "same but different" relationship between mental imagery and vision: imagery activity patterns are transformations of visual activity patterns that approximate them, but encode fewer features and occupy a distinct subspace within the overall space of brain activations.

neuroscience↗

Structural Validation of the Intermediate Leptomeningeal Layer in the Human Central Nervous System

Traditionally, the human central nervous system (CNS) is described as having three meningeal layers, from outer to inner: dura mater, arachnoid mater, and pia mater. The arachnoid and pia mater are called the leptomeninges, and the space between them is filled with cerebrospinal fluid (CSF). Using gross dissection, light microscopy, and ultrastructural analysis of fresh postmortem and cadaveric CNS specimens spanning fetal to adult ages (N=61), we demonstrate a fibrocellular intermediate leptomeningeal layer (ILL) from the cortex to the caudal end of the spinal cord. The ILL divides the subarachnoid space (SAS) into two distinct structural compartments, through which vessels and nerves pass. The ILL shows unique structural features, such as dips into the brains sulci and fissures, as a double-fold membrane that bears intra-layer trabeculae, carries vessels, and forms the perivascular sheath. Moreover, throughout the CNS, it appears to be a non-sieved barrier, characterized by the presence of tight and adherens junctions. ILL, predominantly in the spinal cord, contains macrophage-like cells, indicating its layer-specific immune properties. The ILL warrants recognition as a distinct human meningeal layer with potential barrier and immune functions. SignificanceO_ST_ABSAn Intermediate Leptomeningeal Layer encloses the Central Nervous System in HumansC_ST_ABSThe integrated analysis of our macroscopic, microscopic, and ultrastructural study provides robust support for an intermediate leptomeningeal layer (ILL) in the subarachnoid space (SAS) of the human central nervous system (CNS) along the entire neural axis. The ILL is a fibrocellular macroscopic structure, with restricted permeability, that divides the cerebrospinal fluid (CSF)-filled SAS into two distinct structural compartments. Uniquely, ILL revealed the presence of cells with macrophage-like properties, suggesting a possible role in immune surveillance. The ILL may redefine the established concept of protective coverings of CNS, CSF circulation dynamics, and the role of leptomeninges in health and disease, including drug delivery.

neuroscience↗