HippoGenes provides a framework for exploring the molecular organization of the hippocampus, opening avenues for multiscale integration in health and disease, and is openly available on https://hippogenes.readthedocs.io.
Abstract
The human hippocampus is a unique cortical structure central to brain function, plasticity, and disease. Unravelling its complex organization requires the integration of multiscale data, linking molecular features to mesoscale anatomy and macroscale functional patterns. Gene expression is a fundamental microscale phenotype, and its profiling can provide a reference description of how molecular features are distributed across the brain. Capitalizing on recent imaging-transcriptomic analyses, we introduce HippoGenes, a repository of fine-grained gene expression patterns across human hippocampal subregions. We leveraged spatial statistical models and hippocampal surface mapping to reconstruct dense transcriptomic maps from sparse post-mortem tissue samples of the Allen Human Brain Atlas, generating continuous expression estimates for thousands of genes aligned to a common surface-based coordinate system. We illustrate the utility of HippoGenes to (i) map medial-lateral and anterior-posterior transcriptomic gradients that align with subfield and tripartite subdivisions of the hippocampal formation, (ii) examine associations between gene expression and canonical microstructural and functional features of the hippocampus, and (iii) perform a molecular decoding of subregional alterations in neurological patients with hippocampal pathology. HippoGenes provides a framework for exploring the molecular organization of the hippocampus, opening avenues for multiscale integration in health and disease, and is openly available on https://hippogenes.readthedocs.io/.
A spatial transcriptomic atlas of the human amygdala from nine neurotypical donors provides a foundational resource and framework for accelerating cross-species comparisons and human disease-focused investigations.
Michael S. Totty, Svitlana V. Bach, Madeline R. Valentine et al.· bioRxiv· 0 citations
A comprehensive molecular atlas of HPC and MEC in five species is generated, standardizing the dorsoventral axis for cross-species comparison and revealing both conserved and species-specific dorsoventral programs underlying brain function and evolution.
Sihui Cheng, Qi-Run Wang, Ye Feng et al.· bioRxiv· 0 citations
The results revealed spatially enriched gene sets associated with progenitor proliferation, self-renewal, and neurogenesis, as well as temporal transcriptional enrichment for axonogenesis and extracellular matrix regulation.
M. Barresi, Alice Johnstone, Sebastian Quezada et al.· Brain Structure and Function· 0 citations
This study provides the first whole human brain map of AD pathology-associated transcriptomic signals, and exposes cell type, region, and cortex layer specific vulnerabilities.
Anwesha Bhattacharya, C. Savignac, Liam Hodgson et al.· bioRxiv· 0 citations
Using single-nucleus RNA sequencing across 109 human and 22 mouse samples spanning dorsal and ventral striatum, a comprehensive atlas of subregional neuronal specialization is provided, suggesting divergent pharmacological targets, connectivity, and disease mechanisms.
Raleigh M. Linville, Benjamin T. James, K. Galani et al.· Cell· 2 citations· ⚡1
A "retrodictive" analysis of the cortex is presented that reconstructs the proliferation history of neural stem cells from a static snapshot of tissue, providing a developmentally grounded coordinate system for comparison across samples and is expected to be a foundational framework for 3D neuropathological analysis.
Tatsuya C. Murakami, Nathaniel Heintz· bioRxiv· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.