Mooren Olivia L, Kim Joanna, Li Jinmei, Cooper John A
From the Department of Cell Biology and Physiology, Washington University, St. Louis, Missouri 63110.
From the Department of Cell Biology and Physiology, Washington University, St. Louis, Missouri 63110
J Biol Chem. 2015 Jul 24;290(30):18796-805. doi: 10.1074/jbc.M115.668285. Epub 2015 Jun 12.
Endothelial cells (ECs) form a monolayer that serves as a barrier between the blood and the underlying tissue. ECs tightly regulate their cell-cell junctions, controlling the passage of soluble materials and immune cells across the monolayer barrier. We studied the role of N-WASP, a key regulator of Arp2/3 complex and actin assembly, in EC monolayers. We report that N-WASP regulates endothelial monolayer integrity by affecting the organization of cell junctions. Depletion of N-WASP resulted in an increase in transendothelial electrical resistance, a measure of monolayer integrity. N-WASP depletion increased the width of cell-cell junctions and altered the organization of F-actin and VE-cadherin at junctions. N-WASP was not present at cell-cell junctions in monolayers under resting conditions, but it was recruited following treatment with sphingosine-1-phosphate. Taken together, our results reveal a novel role for N-WASP in remodeling EC junctions, which is critical for monolayer integrity and function.
内皮细胞(ECs)形成一层单层结构,作为血液与下方组织之间的屏障。内皮细胞严格调控其细胞间连接,控制可溶性物质和免疫细胞穿过单层屏障。我们研究了Arp2/3复合物和肌动蛋白组装的关键调节因子N-WASP在内皮细胞单层中的作用。我们报告称,N-WASP通过影响细胞连接的组织来调节内皮单层的完整性。N-WASP的缺失导致跨内皮电阻增加,这是单层完整性的一种度量。N-WASP的缺失增加了细胞间连接的宽度,并改变了连接处F-肌动蛋白和血管内皮钙黏蛋白的组织。在静息条件下,单层中的细胞间连接处不存在N-WASP,但在用1-磷酸鞘氨醇处理后它会被招募。综上所述,我们的结果揭示了N-WASP在重塑内皮细胞连接中的新作用,这对单层的完整性和功能至关重要。