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Blanpain, L.

Publications and source records attributed to Blanpain, L..

2 recordsLinked to original sources

Direct electrical stimulation of the human amygdala enhances recognition memory for objects but not scenes

Research from neuroscience studies using invasive neuroanatomy-inspired direct manipulations suggests the basolateral amygdala (BLA) mediates a generalized modulation of many different types of memory. In contrast, noninvasive, psychology-inspired indirect correlations suggest that specificity exists in how the BLA prioritizes experiences in memory. We used direct electrical stimulation of the BLA to investigate the specificity of the memory enhancement in the human brain. Patients undergoing intracranial monitoring via depth electrodes viewed object and scene images, half of which were followed by BLA stimulation. Stimulation enhanced long-term memory for object but not scene images. Furthermore, BLA stimulation elicited stronger evoked responses in the anterior vs. posterior medial temporal lobe (MTL), regions that preferentially process object and scene learning, respectively. These results suggest the BLA exerts an important influence over the specificity of what information is prioritized in memory, rather than a general enhancement of all memory, and provide insight into how BLA-MTL projections contribute to the dynamics of memory prioritization.

neuroscience↗

Cell type-specific genetic regulation of expression in the granule cell layer of the human dentate gyrus

Laser capture microdissection followed by RNA-seq (LCM-seq) was used to profile the transcriptional landscape of the granule cell layer of the dentate gyrus (DG-GCL) in human hippocampus, and contrasted to homogenate tissue. We identified widespread cell type-specific aging and genetic effects in the DG-GCL that were either missing or directionally discordant in corresponding bulk hippocampus RNA-seq data from largely the same subjects. Of the [~]9 million eQTLs in the DG-GCL, 15% were not in bulk hippocampus, including 15 schizophrenia genome-wide association study (GWAS) risk variants. We then created custom transcriptome-wide association study (TWAS) genetic weights from the DG-GCL which identified many novel schizophrenia-associated genetic signals not found in TWAS from bulk hippocampus, including GRM3 and CACNA1C. These results highlight the biological resolution of cell type-specific expression profiling using targeted sampling strategies like LCM, and complement homogenate and single nuclei approaches in human brain.

neuroscience↗