Multi-scale spatial transcriptomic atlas of the whole mouse spinal cord
- 1University of Southern California
Abstract
The spinal cord coordinates sensory, motor and autonomic functions through diverse neuronal and non-neuronal populations, yet how molecularly defined cell types are organized across its full extent remains incompletely understood. Here we use Stereo-seq to generate a genome-wide, single-cell-resolution spatial atlas of the whole adult mouse spinal cord. Profiling 322,827 cells across 81 anatomically registered transverse sections spanning cervical, thoracic, lumbar and sacral levels, we resolve 12 major cell classes and 94 transcriptomic subclusters. Major cell classes occupy characteristic anatomical territories conserved along the rostrocaudal axis, whereas individual subclusters exhibit reproducible laminar, mediolateral and segment-associated distributions. Transcriptome-wide analysis identifies coordinated spatial gene-expression modules that delineate anatomical domains independently of predefined cell-type labels. Notably, oligodendrocyte subtypes exhibit a distinct and reproducible laminar organization within spinal cord white matter across spinal levels, revealing finer structural subdivisions beyond conventional anatomical descriptions. Integrating cell-type identities with local spatial organization further defines hierarchical domains that recapitulate canonical anatomy while resolving finer subdivisions within established regions. Together, these findings define a multi-scale cellular architecture linking transcriptomic diversity, spatial gene-expression programs and anatomical organization throughout the spinal cord.
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BibTeX
@misc{zhang2026multiscale,
title = {{Multi-scale spatial transcriptomic atlas of the whole mouse spinal cord}},
author = {G.-W. Zhang and J. Li and J. J. Huang and H. W. Tao and K. K. Zhang and L. I. Zhang},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.24.761397},
url = {https://www.biorxiv.org/content/10.64898/2026.10.24.761397v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Multi-scale spatial transcriptomic atlas of the whole mouse spinal cord
AU - G.-W. Zhang
AU - J. Li
AU - J. J. Huang
AU - H. W. Tao
AU - K. K. Zhang
AU - L. I. Zhang
PY - 2026
DA - 2026/10/24
PB - bioRxiv
DO - 10.64898/2026.10.24.761397
UR - https://www.biorxiv.org/content/10.64898/2026.10.24.761397v1
AB - The spinal cord coordinates sensory, motor and autonomic functions through diverse neuronal and non-neuronal populations, yet how molecularly defined cell types are organized across its full extent remains incompletely understood. Here we use Stereo-seq to generate a genome-wide, single-cell-resolution spatial atlas of the whole adult mouse spinal cord. Profiling 322,827 cells across 81 anatomically registered transverse sections spanning cervical, thoracic, lumbar and sacral levels, we resolve 12 major cell classes and 94 transcriptomic subclusters. Major cell classes occupy characteristic anatomical territories conserved along the rostrocaudal axis, whereas individual subclusters exhibit reproducible laminar, mediolateral and segment-associated distributions. Transcriptome-wide analysis identifies coordinated spatial gene-expression modules that delineate anatomical domains independently of predefined cell-type labels. Notably, oligodendrocyte subtypes exhibit a distinct and reproducible laminar organization within spinal cord white matter across spinal levels, revealing finer structural subdivisions beyond conventional anatomical descriptions. Integrating cell-type identities with local spatial organization further defines hierarchical domains that recapitulate canonical anatomy while resolving finer subdivisions within established regions. Together, these findings define a multi-scale cellular architecture linking transcriptomic diversity, spatial gene-expression programs and anatomical organization throughout the spinal cord.
ER -