Urea functions as a risk signal driving astrocyte-mediated neuroinflammation following stroke
Year: 2025
Type: article
Abstract: Urea, traditionally recognized as the final product of protein metabolism and a regulator of urine concentration, has recently emerged as a potential contributor to central nervous system (CNS) pathologies. However, its role in ischemic stroke remains largely unexplored. In this study, we identify urea as a previously unrecognized risk signal, whose levels rapidly increase in the brain following ischemic stroke. Elevated urea triggers the induction of neurotoxic A1-type astrocytes and promotes neuronal pyroptosis. Mechanistically, this process is mediated by the astrocytic urea transporter UT-B, which facilitates urea influx and initiates a cascade of neuroinflammatory responses. Through quantitative proteomics and gene silencing, we further demonstrate that urea exacerbates DNA damage via activation of the transcriptional coactivator Wwtr1, thereby amplifying the generation of A1 astrocytes. Collectively, our findings reveal a novel pathophysiological role for urea in ischemic brain injury and underscore the critical involvement of astrocytes in modulating neuroinflammation and neuronal death.
Source: Journal of Neuroinflammation
Authors: Yang Han, Tongshuai Zhang, Dandan Wang, Shanshan Yang, Yixiang Jiang, Yao Zhang, Fan Zhu, Haiquan Tao, Liwei Zhao, Xianfeng Li, Xianfeng Li, Haicheng Yang, Jing Lan, Jiachen He, Changyong Tang, Baoxue Yang, Guangzhi Wang, Xuan Li, Xuan Li, Guangyou Wang
Institutions: Harbin Medical University, First Affiliated Hospital of Harbin Medical University, Southern Medical University, Zhuhai People's Hospital, Third Affiliated Hospital of Harbin Medical University, Second Affiliated Hospital of Harbin Medical University, Third Affiliated Hospital of Sun Yat-sen University, Peking University
Language: English
Subfield: Neurology
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $4,090
Awards: G4356477926, G8277879347
OpenAlex ID: W4416563678
