粘合连接
紧密连接
淋巴系统
细胞生物学
封堵器
细胞结
拉链
普氏球蛋白
淋巴管内皮
生物
VE钙粘蛋白
内皮
解剖
缝隙连接
克洛丹
钙粘蛋白
免疫学
信号转导
细胞
细胞内
连环素
内分泌学
Wnt信号通路
遗传学
算法
计算机科学
作者
Peter Bałuk,Donald M. McDonald
出处
期刊:Cold Spring Harbor Perspectives in Medicine
[Cold Spring Harbor Laboratory]
日期:2022-05-09
卷期号:: a041178-a041178
被引量:17
标识
DOI:10.1101/cshperspect.a041178
摘要
Button-like junctions are discontinuous contacts at the border of oak-leaf-shaped endothelial cells of initial lymphatic vessels. These junctions are distinctively different from continuous zipper-like junctions that create the endothelial barrier in collecting lymphatics and blood vessels. Button junctions are point contacts, spaced about 3 µm apart, that border valve-like openings where fluid and immune cells enter lymphatics. In intestinal villi, openings between button junctions in lacteals also serve as entry routes for chylomicrons. Like zipper junctions that join endothelial cells, buttons consist of adherens junction proteins (VE-cadherin) and tight junction proteins (claudin-5, occludin, and others). Buttons in lymphatics form from zipper junctions during embryonic development, can convert into zippers in disease or after experimental genetic or pharmacological manipulation, and can revert back to buttons with treatment. Multiple signaling pathways and local microenvironmental factors have been found to contribute to button junction plasticity and could serve as therapeutic targets in pathological conditions ranging from pulmonary edema to obesity.
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