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Biology subjects

Kooijmans, R. N.

Publications and source records attributed to Kooijmans, R. N..

3 recordsLinked to original sources

Brain FACTs: A same-section workflow for Fiber Architecture, Cytoarchitecture and cell Types in large-scale brain sections

Understanding the human brain's multiscale organization requires linking cells, connections and architecture, yet conventional methods are incompatible within a single specimen, and inter-individual variability confounds cross-brain comparisons. Multiple-label immunohistochemistry for different cell types has been applied in interleaved sections but remains challenging within a single large human brain section and, has never been combined on the same tissue with 3D polarized light imaging (3D-PLI) for three-dimensional fiber architecture. Here we introduce a sequential multimodal workflow integrating 3D-PLI, multiplex chromogenic immunohistochemistry and Nissl staining on the same large human brain section, preserving each technique's quality and specificity. The method was validated on vervet monkey and Wistar rat sections. The resulting paired high-resolution images eliminate inter-subject variability and enable direct micron-scale mapping of fiber tracts relative to molecularly defined cell types, yielding previously inaccessible insights such as molecular identification of white-matter components, refined cortical layering and cytoarchitectural disambiguation.

neuroscience↗

Friend, not Foe: Lowered Tissue Reactivity to Long-Term Polyimide Implants

One of the biggest challenges for neurotechnology is the design of devices that are tolerated well by brain tissue, without sacrificing functionality and implantability. This study examined which design choices mitigate tissue damage and improve longevity, by varying probe features implanted in the cerebral cortex of mice. We report on a systematic, quantitative analysis of neuronal and inflammation markers across cortical depth. We implanted a total of 103 stiff silicon or flexible polyimide probes in 32 mice, varying their thicknesses and widths, which were either attached to the skull or not. A new, automated workflow to quantify immunohistochemical data examines: 1) the tissue loss caused by the implant, 2) the cortical neuronal density, and 3) the immune response expressed by astrocytic and microglial reaction. Flexible polyimide probes exhibited a clear advantage, with fewer lesions and weaker immune responses than stiff silicon probes. Furthermore, we observed a weaker influence of the shank cross-section. A cortical depth profile of immune reactivity revealed focal reactions at the device entry points in the superficial cortex and at the cortex-white matter boundary. This study gives important insights on optimizing device design parameters as well as surgical insights for improved tissue integration of intracortical electrode arrays.

bioengineering↗

5’ tRNA halves are highly expressed in the primate hippocampus and sequence-specifically regulate gene expression

Fragments of mature tRNAs have long been considered as mere degradation products without physiological function. However, recent reports show that tRNA fragments (tRFs) play prominent roles in diverse cellular processes across a wide spectrum of species. Contrasting the situation in other small RNA pathways the mechanisms behind these effects appear more diverse, more complex and are generally less well understood. In addition, surprisingly little is known about the expression profiles of tRFs across different tissues and species. Here, we provide an initial overview of tRF expression in different species and tissues, revealing very high tRF-levels particularly in the primate hippocampus. We further modulated the regulation capacity of selected tRFs in human cells by transfecting synthetic tRF mimics (\"overexpression\") or antisense-RNAs (\"inhibition\") and identified differentially expressed transcripts based on RNAseq. We then used a novel k-mer mapping approach to dissect the underlying targeting rules, demonstrating that 5 tRNA halves (5 tRHs) silence genes in a sequence-specific manner, while the most efficient target sites align to the mid-region of the 5 tRH and are located within the CDS or 3 UTR of the target. This amends previous observations that tRFs guide Argonaut proteins to silence their targets via a miRNA-like 5 seed match and suggests a yet unknown mechanism of regulation. Finally, our data suggests that some 5 tRHs are also able to sequence-specifically stabilize mRNAs as upregulated mRNAs are also significantly enriched for 5 tRH target sites.

molecular biology↗