粘合连接
紧密连接
细胞生物学
细胞结
封堵器
并行传输
钙粘蛋白
机械转化
血管通透性
生物
内皮干细胞
肌动蛋白细胞骨架
VE钙粘蛋白
细胞骨架
细胞粘附
化学
细胞
磁导率
生物化学
体外
内分泌学
膜
作者
Ken D. Brandon,William E. Frank,Kimberly M. Stroka
出处
期刊:American Journal of Physiology-cell Physiology
[American Physical Society]
日期:2024-08-12
卷期号:327 (4): C1073-C1086
被引量:5
标识
DOI:10.1152/ajpcell.00605.2023
摘要
Cells depend on precisely regulating barrier function within the vasculature to maintain physiological stability and facilitate essential substance transport. Endothelial cells achieve this through specialized adherens and tight junction protein complexes, which govern paracellular permeability across vascular beds. Adherens junctions, anchored by vascular endothelial (VE)-cadherin and associated catenins to the actin cytoskeleton, mediate homophilic adhesion crucial for barrier integrity. In contrast, tight junctions composed of occludin, claudin, and junctional adhesion molecule A interact with Zonula Occludens proteins, reinforcing intercellular connections essential for barrier selectivity. Endothelial cell-cell junctions exhibit dynamic conformations during development, maturation, and remodeling, regulated by local biochemical and mechanical cues. These structural adaptations play pivotal roles in disease contexts such as chronic inflammation, where junctional remodeling contributes to increased vascular permeability observed in conditions from cancer to cardiovascular diseases. Conversely, the brain microvasculature's specialized junctional arrangements pose challenges for therapeutic drug delivery due to their unique molecular compositions and tight organization. This commentary explores the molecular mechanisms underlying endothelial cell-cell junction conformations and their implications for vascular permeability. By highlighting recent advances in quantifying junctional changes and understanding mechanotransduction pathways, we elucidate how physical forces from cellular contacts and hemodynamic flow influence junctional dynamics.
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