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AKAP12 regulates vascular integrity in zebrafish

机译:AKAP12调节斑马鱼的血管完整性

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摘要

The integrity of blood vessels controls vascular permeability and extravasation of blood cells, across the endothelium. Thus, the impairment of endothelial integrity leads to hemorrhage, edema, and inflammatory infiltration. However, the molecular mechanism underlying vascular integrity has not been fully understood. Here, we demonstrate an essential role for A-kinase anchoring protein 12 (AKAP12) in the maintenance of endothelial integrity during vascular development. Zebrafish embryos depleted of akap12 (akap12 morphants) exhibited severe hemorrhages. In vivo time-lapse analyses suggested that disorganized interendothelial cell-cell adhesions in akap12 morphants might be the cause of hemorrhage. To clarify the molecular mechanism by which the cell-cell adhesions are impaired, we examined the cell-cell adhesion molecules and their regulators using cultured endothelial cells. The expression of PAK2, an actin cytoskeletal regulator, and AF6, a connector of intercellular adhesion molecules and actin cytoskeleton, was reduced in AKAP12-depleted cells. Depletion of either PAK2 or AF6 phenocopied AKAP12-depleted cells, suggesting the reduction of PAK2 and AF6 results in the loosening of intercellular junctions. Consistent with this, overexpression of PAK2 and AF6 rescued the abnormal hemorrhage in akap12 morphants. We conclude that AKAP12 is essential for integrity of endothelium by maintaining the expression of PAK2 and AF6 during vascular development.
机译:血管的完整性控制整个内皮的血管通透性和血细胞外渗。因此,内皮完整性的损害导致出血,水肿和炎性浸润。但是,尚未完全了解血管完整性的分子机制。在这里,我们展示了A激酶锚定蛋白12(AKAP12)在维持血管发育过程中内皮完整性方面的重要作用。耗尽akap12(akap12 morphant)的斑马鱼胚胎表现出严重的出血。体内延时分析表明,akap12 morphant中紊乱的内皮细胞间细胞粘附可能是出血的原因。为了阐明破坏细胞-细胞粘附的分子机制,我们使用培养的内皮细胞检查了细胞-细胞粘附分子及其调节剂。 AKAP12缺失的细胞中,肌动蛋白细胞骨架调节剂PAK2和细胞间粘附分子与肌动蛋白细胞骨架的连接体AF6的表达降低。 PAK2或AF6表型复制的AKAP12缺失的细胞的耗竭,表明PAK2和AF6的减少导致细胞间连接的松动。与此相一致的是,PAK2和AF6的过量表达挽救了akap12吗啡异常出血。我们得出结论,AKAP12通过在血管发育过程中维持PAK2和AF6的表达对于内皮完整性至关重要。

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