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Gosselink, M.

Publications and source records attributed to Gosselink, M..

2 recordsLinked to original sources

Challenging the classical view of CSF flow: measuring CSF net velocity in the human subarachnoid space with 7T MRI

Traditionally, cerebrospinal fluid (CSF) is believed to exit the brain via arachnoid villi, being absorbed into the superior sagittal sinus (SSS), with a net flow towards these exit sites driven by constant CSF turnover. However, measuring these velocities non-invasively in humans is challenging due to their slow nature and the presence of relatively large confounding factors such as physiological CSF pulsations (heartbeat and respiration) and head motion. This study presents a novel magnetic resonance imaging (MRI) method designed to measure the net velocity of CSF whilst accounting for confounding effects, which is called CSF displacement encoding with stimulated echoes (CSF-DENSE). By applying a similar model as used to study sea-level rise, different motion components of CSF were successfully disentangled. Simulations, along with phantom and in vivo experiments, demonstrate the ability of CSF-DENSE combined with time series analysis using unobserved components modeling to detect ultraslow velocities of approximately 1 μm/s, even in the presence of confounding motions that are an order of magnitude larger. If the major egress of CSF were via the SSS, the expected net velocity towards the SSS was estimated to be 4.22±0.14 µm/s, based on measured CSF net flow through the aqueduct into the subarachnoid space (SAS). However, no significant net velocity toward the SSS was observed (v = -0.18±0.15 µm/s, with positive velocity directed towards the SSS), thereby challenging the classical view of CSF outflow. These findings suggest the need to reconsider traditional models of CSF outflow pathways, with potential implications for understanding and treating neurological disorders.

neuroscience↗

An in situ quantitative map of initial human colorectal HIV transmission

The initial immune response to HIV is critical in determining transmission. However, due to technical limitations we still do not have a comparative map of early mucosal transmission events. We combined RNAscope, cyclic-immunofluorescence and novel image analysis tools to quantify HIV transmission dynamics in intact human colorectal tissue. We mapped HIV enrichment to mucosal dendritic cells (DC) and submucosal macrophages, but not CD4+ T-cells, the primary targets of downstream infection. DCs appeared to funnel virus to lymphoid aggregates which acted as early sanctuaries of high viral titres whilst facilitating HIV passage to the submucosa. Finally, HIV entry induced rapid recruitment and clustering of target cells, facilitating DC and macrophage mediated HIV transfer and enhanced infection of CD4+ T-cells. These data demonstrate a rapid response to HIV structured to maximise the likelihood of mucosal infection, and provide a framework for in situ studies of host pathogen interactions and immune mediated pathologies. Highlights- in situ quantification of host cellular microenvironment response to pathogen invasion in human colorectal tissue. - HIV first localises to mucosal DCs and submucosal macrophages, but not CD4+ T cells. - Viral enrichment first occurs in lymphoid aggregates which is associated with passage into the submucosa. - Early localisation of HIV to CD4+ T cells is associated with interactions with DCs and macrophages. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=200 SRC="FIGDIR/small/490175v1_ufig1.gif" ALT="Figure 1"> View larger version (67K): org.highwire.dtl.DTLVardef@ef8000org.highwire.dtl.DTLVardef@1bc8ed7org.highwire.dtl.DTLVardef@45ddbdorg.highwire.dtl.DTLVardef@e0a57c_HPS_FORMAT_FIGEXP M_FIG C_FIG

immunology↗