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Spatial transcriptomic profiling reveals cortical gene expression alterations after CHIMERA traumatic brain injury in male cFosTRAP2 mice

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DataCite Commons2026-01-06 更新2026-05-06 收录
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https://odc-tbi.org/data/1406
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STUDY PURPOSE: Traumatic Brain Injury (TBI) is a leading cause of global death and disability. The purpose of this study was to identify TBI-induced gene expression changes in mouse brain. The closed-head impact model of engineered rotational acceleration (CHIMERA) was used to induce TBI in cFosTRAP2 mice (aged 3-4 months). A mild TBI was induced using CHIMERA where no skull fracture, structural damage or vascular haemorrhages was caused. DATA COLLECTED: We investigated transcriptomic changes in male cFosTRAP2 mouse brain at 7 days after a mild CHIMERA injury (2.1J impact energy) using 10x genomics Visium spatial transcriptomics technology (n=2 Sham, n=2 TBI). Spatial gene expression data was acquired from 2 sections (bregma -1.80mm and -3.2 mm) from each mouse brain and analyzed using the Seurat R package. We obtained transcriptomic information with strong replicate reproducibility for 55-µm circular regions tiling entire brain sections (2 sections/mouse/condition; 4992 sequenced regions/section; ~40,000 RNA-seq datasets). The dataset of greater than 1B reads yielded cell clusters with region-specific dysregulation of genes and a subset of data representing CHIMERA TBI responsive regions is presented here. Here we present data acquired using Seurat spatial transcriptomics workflow that tabulated fold changes and FDRs for genes that were differentially expressed in cortical cluster (upon integration of spots from both groups). The fold changes were derived from pooled Visium data, where spots from all animals within each experimental group were integrated using Seurat prior to clustering and differential expression analysis. Thus, the reported average log two fold changes reflect group-level (pooled) expression patterns rather than per-animal averages. All raw and processed spatial transcriptomics data, including per-sample Visium outputs, are available through the NCBI Gene Expression Omnibus under accession number GSE282909. This repository includes count matrices, spatial coordinates, and sample level metadata to enable independent reanalysis. DATA USAGE NOTES:
提供机构:
Open Data Commons for Traumatic Brain Injury (ODC-TBI)
创建时间:
2026-01-06
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