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Claeys, W.

Publications and source records attributed to Claeys, W..

2 recordsLinked to original sources

Subtle Pupil-Size Changes Associated With Exploration Do Not Affect Visual Sensitivity

When we feel restless and easily distracted, continuously switching tasks (exploration), our pupils tend to be large. In contrast, when we are calmly focused on a single task (exploitation), our pupils tend to be small. According to the Adaptive Gain Theory (AGT), a switch from exploitation to exploration is associated with an increase in norepinephrine in the locus coeruleus, which in turn triggers pupil dilation. However, the AGT does not provide a functional explanation of why exploration triggers pupil dilation. One possibility is that visual sensitivity, which increases with pupil size, is especially important during exploration. We set out to provide evidence consistent with this functional explanation, as well as to replicate two key previous results. Participants performed a four-armed bandit task, which induces both exploration and exploitation behavior. During the task, participants also needed to detect an occasional and unpredictable near-threshold peripheral flash. We replicated two key results: pupils were larger during exploration than during exploitation; and increased pupil size (overall, independent of exploration status) was associated with increased visual sensitivity. However, most importantly, we did not find that visual sensitivity was higher during exploration than during exploitation; probably, the reliable-yet-tiny increase in pupil size during exploration was too small to affect visual sensitivity. We conclude that key previous results are replicable; however, common experimental paradigms, such as the four-armed bandit task, induce only small changes in exploration behavior. Therefore, more powerful paradigms are required in order to test functional explanations of pupil-size changes during exploration and exploitation.

animal behavior and cognition↗

Newly discovered base barrier cells provide compartmentalization of choroid plexus, brain and CSF

The choroid plexus (ChP) is a highly understudied structure of the central nervous system (CNS). The structure hangs in the brain ventricles, is composed of an epithelial cell layer, which produces the cerebrospinal fluid (CSF) and forms the blood-CSF barrier. It encapsulates a stromal mix of fenestrated capillaries, fibroblasts and a broad range of immune cells. Here, we report that the ChP base region harbors unique fibroblasts that cluster together, are connected by tight junctions and seal the ChP stroma from brain and CSF, thereby forming ChP base barrier cells (ChP BBCs). ChP BBCs are derived from meningeal mesenchymal precursors, arrive early during embryonic development, are maintained throughout life and are conserved across species. Moreover, we provide transcriptional profiles and key markers to label ChP BBCs and observe a striking transcriptional similarity with meningeal arachnoid barrier cells (ABCs). Finally, we provide evidence that this fibroblast cluster functions as a barrier to control communication between CSF and the ChP stroma and between the latter and the brain parenchyma. Moreover, loss of barrier function was observed during an inflammatory insult. Altogether, we have identified a novel barrier that provides functional compartmentalization of ChP, brain and CSF. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=146 SRC="FIGDIR/small/601696v1_ufig1.gif" ALT="Figure 1"> View larger version (47K): org.highwire.dtl.DTLVardef@181e787org.highwire.dtl.DTLVardef@1875f33org.highwire.dtl.DTLVardef@7b2bcdorg.highwire.dtl.DTLVardef@78baa6_HPS_FORMAT_FIGEXP M_FIG Newly discovered base barrier cells provide compartmentalization of choroid plexus, brain and CSF The choroid plexus (ChP) hangs in the brain ventricles and is composed of an epithelial cell layer which produces the cerebrospinal fluid (CSF) and forms the blood-CSF barrier. The ChP epithelial cells are continuous with the ependymal cells lining the ventricle wall. At this base region, we identified and characterized a novel subtype of fibroblasts coined the ChP base barrier cells (BBCs). ChP BBCs express tight junctions (TJs), cluster together and seal the ChP stroma from CSF and brain parenchyma. The subarachnoid space (SAS) CSF penetrates deep into choroid plexus invaginations where it is halted by ChP BBCs. Abbreviations: E9-16.5 (embryonic day 9-16.5); P1-4 (postnatal day 1-4). C_FIG

neuroscience↗