克洛丹
血脑屏障
紧密连接
并行传输
增强子
封堵器
神经科学
血管通透性
势垒函数
医学
生物
药理学
流出
埃文斯蓝
磁导率
肠道通透性
细胞生物学
跨细胞
中枢神经系统
病理
基因表达
生物化学
基因
膜
作者
Yosuke Hashimoto,Matthew Campbell,Keisuke Tachibana,Yoshiaki Okada,Masuo Kondoh
标识
DOI:10.1248/bpb.b21-00408
摘要
Claudin-5 is the dominant tight junction protein in brain endothelial cells and exclusively limits the paracellular permeability of molecules larger than 400 Da across the blood-brain barrier (BBB). Its pathological impairment or sustained down-regulation has been shown to lead to the progression of psychiatric and neurological disorders, whereas its expression under physiological conditions prevents the passage of drugs across the BBB. While claudin-5 enhancers could potentially act as vascular stabilizers to treat neurological diseases, claudin-5 inhibitors could function as delivery systems to enhance the brain uptake of hydrophilic small-molecular-weight drugs. Therefore, the effects of claudin-5 manipulation on modulating the BBB in different neurological diseases requires further examination. To manipulate claudin-5 expression levels and function, several claudin-5 modulating molecules have been developed. In this review, we first describe the molecular, cellular and pathological aspects of claudin-5 to highlight the mechanisms of claudin-5 enhancers/inhibitors. We then discuss recently developed claudin-5 enhancers/inhibitors and new methods to discover these molecules.
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