神经炎症
小胶质细胞
粘合连接
血脑屏障
炎症
神经科学
血管生成
免疫系统
转录因子
多发性硬化
发病机制
生物
癌症研究
医学
中枢神经系统
免疫学
细胞
基因
钙粘蛋白
生物化学
遗传学
作者
Elham Poonaki,Ulf D. Kahlert,Sven G. Meuth,Ali Gorji
标识
DOI:10.1186/s12974-022-02636-2
摘要
Abstract Zinc finger E-box binding homeobox 1 (ZEB1) is a master modulator of the epithelial–mesenchymal transition (EMT), a process whereby epithelial cells undergo a series of molecular changes and express certain characteristics of mesenchymal cells. ZEB1, in association with other EMT transcription factors, promotes neuroinflammation through changes in the production of inflammatory mediators, the morphology and function of immune cells, and multiple signaling pathways that mediate the inflammatory response. The ZEB1–neuroinflammation axis plays a pivotal role in the pathogenesis of different CNS disorders, such as brain tumors, multiple sclerosis, cerebrovascular diseases, and neuropathic pain, by promoting tumor cell proliferation and invasiveness, formation of the hostile inflammatory micromilieu surrounding neuronal tissues, dysfunction of microglia and astrocytes, impairment of angiogenesis, and dysfunction of the blood–brain barrier. Future studies are needed to elucidate whether the ZEB1–neuroinflammation axis could serve as a diagnostic, prognostic, and/or therapeutic target for CNS disorders.
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