Junctions at the Crossroads: The Impact of Mechanical Cues on Endothelial Cell-Cell Junction Conformations and Vascular Permeability

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
作者
Ken D. Brandon,William E. Frank,Kimberly M. Stroka
出处
期刊:American Journal of Physiology-cell Physiology [American Physical Society]
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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