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Protocol to evaluate mouse brain spatial cell type-resolved transcriptomic discoveries using 10x Visium spatial transcriptomics and FLEX scRNA-seq
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DOI：10.1016/j.xpro.2025.104277.png)
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Abstract
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Understanding changes in gene expression and cell-cell signaling among spatial regions in diseased tissues adds critical biological information to understanding mechanisms. Here, we present a protocol to investigate molecular transcriptional drivers within intact murine tissue using 10x Genomics Visium spatial transcriptomics and 10x Genomics FLEX single-cell RNA sequencing (scRNA-seq) data. We describe steps for collecting mouse brain tissue from multiple ages, processing samples, and mounting the tissue. We then detail procedures for staining, FLEX tissue section collection, fixation, dissociation, and cell storage. For complete details on the use and execution of this protocol, please refer to Burns et al.1
Keywords:
spatial transcriptomics
single-cell RNA sequencing
mouse brain
gene expression
cell-cell signaling
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