Brain–cervical lymph node crosstalk contributes to brain injury induced by subarachnoid hemorrhage in mice

Cross-talk between the brain and cervical lymph nodes (CLNs) is crucial in brain pathologies. However, the precise roles and the mechanisms of CLNs in brain damage during subarachnoid hemorrhage (SAH) remain unclear. In this study, mandibular lymph node (part of CLNs) removal attenuates brain damage in SAH mouse models. Notably, the extravasated erythrocytes following SAH are significantly engulfed by lymphatic endothelial cells (LECs) in CLNs. Single-cell RNA sequencing reveals that the differentially expressed genes in medullary LECs are enriched in lysosomes after SAH, with a notable upregulation of Ctss (which encodes cathepsin S). Importantly, the deficiency of cathepsin S specifically in LECs, achieved through transgenic mice, or the use of a cathepsin S inhibitor, significantly reduces neuroinflammation and neurological deficits induced by SAH. These findings elucidate mechanisms of how CLNs participate in brain injury following SAH in mice. Targeting this process may offer effective therapeutic strategies to alleviate SAH-related pathologies.

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Journal
Nature Communications
Published
2025-09-29
DOI
https://doi.org/10.1038/s41467-025-63544-6
Citations
1
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.84
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article

Brain–cervical lymph node crosstalk contributes to brain injury induced by subarachnoid hemorrhage in mice

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1 citations
Nature Communications
Neuroinflammation and Neurodegeneration Mechanisms
0.84
article

Brain–cervical lymph node crosstalk contributes to brain injury induced by subarachnoid hemorrhage in mice

Tianhao Xu, Qi Shi, Lianping Xing, Wenchao Ding, Zixin Zhuang, YongJun Wang, Qianqian Liang, Jinman Chen, Jie Wang, Yongjian Zhao, Ning Li, Wenjing Zheng, Hao Xu, Linmei Wang, Wenhao Ding
article en
1 citations

Abstract

Cross-talk between the brain and cervical lymph nodes (CLNs) is crucial in brain pathologies. However, the precise roles and the mechanisms of CLNs in brain damage during subarachnoid hemorrhage (SAH) remain unclear. In this study, mandibular lymph node (part of CLNs) removal attenuates brain damage in SAH mouse models. Notably, the extravasated erythrocytes following SAH are significantly engulfed by lymphatic endothelial cells (LECs) in CLNs. Single-cell RNA sequencing reveals that the differentially expressed genes in medullary LECs are enriched in lysosomes after SAH, with a notable upregulation of Ctss (which encodes cathepsin S). Importantly, the deficiency of cathepsin S specifically in LECs, achieved through transgenic mice, or the use of a cathepsin S inhibitor, significantly reduces neuroinflammation and neurological deficits induced by SAH. These findings elucidate mechanisms of how CLNs participate in brain injury following SAH in mice. Targeting this process may offer effective therapeutic strategies to alleviate SAH-related pathologies.

Nature CommunicationsVol. 16(1)
University of Rochester Medical Center (US), Wuhan University (CN), Shanghai University of Traditional Chinese Medicine (CN), Longhua Hospital Shanghai University of Traditional Chinese Medicine (CN), Fifth Hospital In Wuhan (CN)
Openalex Percentile: Top 21%
Neuroinflammation and Neurodegeneration Mechanisms
0.84
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