文献类型: 外文期刊
作者: Fang, Chuantao;Zhang, Xiaodan;Yang, Lin;Sun, Licheng;Lu, Yujia;Liu, Yi;Guo, Jingjing;Wang, Min;Tan, Yanfeng;Zhang, Jinsen;Gao, Xin;Zhu, Li;Liu, Guoping;Ren, Maozhi;Xiao, Jianbo;Zhang, Fayong;Ma, Shaojie;Zhao, Rui;Mei, Xinyu;Qi, Dashi
作者机构:
期刊名称: NATURE COMMUNICATIONS
ISSN:
年卷期: 2025 年 16 卷 1 期
页码:
收录情况: SCIE(2025版)
摘要: Focal cortical dysplasia type II (FCDII) is a major cause of drug-resistant epilepsy, but genetic factors explain only some cases, suggesting other mechanisms. In this study, we conduct a molecular analysis of brain lesions and adjacent areas in FCDIIb patients. By analyzing over 217,506 single-nucleus transcriptional profiles from 15 individuals, we find significant changes in smooth muscle cells (SMCs) and astrocytes. We identify abnormal vascular malformations and a unique type of SMC that we call Firework cells, which migrate from blood vessels into the brain parenchyma and associate with VIM+ cells. These abnormalities create localized ischemic-hypoxic (I/H) microenvironments, as confirmed by clinical data, further impairing astrocyte function, activating the HIF-1 alpha/mTOR/S6 pathway, and causing neuronal loss. Using zebrafish models, we demonstrate that vascular abnormalities resulting in I/H environments promote seizures. Our results highlight vascular malformations as a factor in FCDIIb pathogenesis, suggesting potential therapeutic avenues.
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