Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder

Alcohol use disorder (AUD) induces complex transcriptional and regulatory changes across multiple brain regions including the caudate nucleus, which remains understudied. Using paired single-nucleus RNA-seq and ATAC-seq on caudate samples from 143 human postmortem brains, including 74 with AUD, we identified 17 distinct cell types. A significant portion of the alcohol-related differences in gene expression were accompanied by a corresponding difference in chromatin accessibility within the gene. We observed transcriptional differences in medium spiny neurons that impact RNA metabolism and immune response pathways. A small cluster of D1/D2 hybrid neurons showed AUD-induced differences distinct from the D1 and D2 types, suggesting a unique role in AUD. Those with AUD had a higher proportion of microglia in an inflammatory state; astrocytes entered a reactive state partially regulated by JUND. Oligodendrocyte dysregulation was driven in part by OLIG2 activity and increased TGF-β1 signaling from microglia and astrocytes. We also observed increased microglia-astrocyte communication via the IL-1β pathway. These findings provide valuable insights into the genetic and cellular mechanisms in the caudate related to AUD. They also demonstrate the broader utility of large-scale multiomic studies in uncovering complex gene regulation across diverse cell types, which has implications beyond the substance use field.

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Publication Details

Journal
Nature Communications
Published
2025-10-13
DOI
https://doi.org/10.1038/s41467-025-64136-0
Citations
5
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
4.21

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article

Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder

Xiaoling Xuei, Qiuyue Yuan, Guanglong Jiang, Zhiping P. Pang et al.
5 citations
Nature Communications
Neuroinflammation and Neurodegeneration Mechanisms
4.21
article

Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder

Xiaoling Xuei, Qiuyue Yuan, Guanglong Jiang, Zhiping P. Pang, Greg T. Sutherland, Arpana Agrawal, Zhana Duren, Jay A. Tischfield, Howard J. Edenberg, Ronald P. Hart, Patrick C. McGuire, Julia Stevens, Dongbing Lai, Jill L. Reiter, Paul A. Slesinger, Alison Goate, Yunlong Liu, Yue Wang, Hongyu Gao, Nick Green, Xiaona Chu
article en
5 citations

Abstract

Alcohol use disorder (AUD) induces complex transcriptional and regulatory changes across multiple brain regions including the caudate nucleus, which remains understudied. Using paired single-nucleus RNA-seq and ATAC-seq on caudate samples from 143 human postmortem brains, including 74 with AUD, we identified 17 distinct cell types. A significant portion of the alcohol-related differences in gene expression were accompanied by a corresponding difference in chromatin accessibility within the gene. We observed transcriptional differences in medium spiny neurons that impact RNA metabolism and immune response pathways. A small cluster of D1/D2 hybrid neurons showed AUD-induced differences distinct from the D1 and D2 types, suggesting a unique role in AUD. Those with AUD had a higher proportion of microglia in an inflammatory state; astrocytes entered a reactive state partially regulated by JUND. Oligodendrocyte dysregulation was driven in part by OLIG2 activity and increased TGF-β1 signaling from microglia and astrocytes. We also observed increased microglia-astrocyte communication via the IL-1β pathway. These findings provide valuable insights into the genetic and cellular mechanisms in the caudate related to AUD. They also demonstrate the broader utility of large-scale multiomic studies in uncovering complex gene regulation across diverse cell types, which has implications beyond the substance use field.

Nature CommunicationsVol. 16(1)
Rutgers, The State University of New Jersey (US), Washington University in St. Louis (US), Johnson University (US), Southern University of Science and Technology (CN), UNSW Sydney (AU), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US), Icahn School of Medicine at Mount Sinai (US)
Children's Hospital of Philadelphia, University of Pennsylvania, State University of New York, Washington University in St. Louis, University of Connecticut, University of Sydney, National Institutes of Health, SUNY Downstate Medical Center, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, National Institute on Alcohol Abuse and Alcoholism, National Institute on Drug Abuse
Openalex Percentile: Top 5%
Neuroinflammation and Neurodegeneration Mechanisms
4.21
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