2026-09-01 マサチューセッツ工科大学(MIT)
<関連情報>
- https://news.mit.edu/2026/brains-striatum-atlas-could-guide-researchers-new-drug-treatments-0901
- https://www.cell.com/cell/abstract/S0092-8674(26)00933-5
線条体の種間単一細胞アトラスにより、細胞型および亜領域の疾患脆弱性が明らかになる Cross-species single-cell atlas of the striatum defines cell-type and subregion disease vulnerabilities
Raleigh M. Linville ∙ Benjamin T. James ∙ Kyriaki Galani ∙ … ∙ Dana Gabuzda ∙ Manolis Kellis, ∙ Myriam Heiman
Cell Published:September 1, 2026
DOI:https://doi.org/10.1016/j.cell.2026.08.006
Highlights
- Single-cell profiling maps human striatal neuron diversity and subregion specialization
- Cross-species comparison reveals key human-rodent differences in striatal cell types
- GWAS and pharmacology map cell types for addiction risk and antipsychotic response
- scMOSAIC unravels subregional and cell-type vulnerabilities in Huntington’s disease

Summary
The striatum is critical for decision-making, movement, and reward processing, functions achieved through subregional cellular and molecular specialization. Striatal cell types and subregions are differentially implicated in neurodegenerative and neuropsychiatric disorders, but the mechanisms underlying these vulnerabilities are poorly understood. Using single-nucleus RNA sequencing across 109 human and 22 mouse samples spanning dorsal and ventral striatum, we provide a comprehensive atlas of subregional neuronal specialization. We define rare neuronal subpopulations and transcriptional gradients along the dorsolateral-ventromedial axis with notable differences between species, suggesting divergent pharmacological targets, connectivity, and disease mechanisms. Integration with genome-wide association and pharmacological studies identifies human-enriched sites of opioid receptor expression and ventral-biased chronic antipsychotic action. Lastly, paired single-cell transcriptomic and somatic trinucleotide repeat expansion measurements identify differences in subregion and neuronal subtype vulnerability in Huntington’s disease. Our findings lay the foundation for understanding how striatal cell types and subregions contribute to brain function and neurological disorders.

