Suppr超能文献

内皮剪切应力受损通过上调VEGF诱导足体组装。

Impaired endothelial shear stress induces podosome assembly via VEGF up-regulation.

作者信息

Fey Theres, Schubert Kai Michael, Schneider Holger, Fein Evelyn, Kleinert Eike, Pohl Ulrich, Dendorfer Andreas

机构信息

Walter-Brendel-Centre of Experimental Medicine, Ludwig-Maximilians-Universität München, Munich, Germany;

Walter-Brendel-Centre of Experimental Medicine, Ludwig-Maximilians-Universität München, Munich, Germany; German Centre for Cardiovascular Research (DZHK)-Munich Heart Alliance, Munich, Germany; Munich Cluster for Systems Neurology, Munich, Germany.

出版信息

FASEB J. 2016 Aug;30(8):2755-66. doi: 10.1096/fj.201500091R. Epub 2016 Apr 21.

Abstract

Podosomes are dynamic cytoskeletal membrane structures with local adhesive and proteolytic activity. They are critically involved in angiogenesis and vascular adaptive growth. Here, we studied in HUVECs and murine small vessels whether shear stress controls podosome assembly and local proteolytic activity. Podosomes were characterized by immunohistochemistry, and their proteolytic activity was assessed as degradation imprints in fluorescent gelatin that was used as growth substrate. Compared with controls (10 dyn/cm(2)), the number of podosomes formed per time was doubled when cells were exposed to low shear stress (0.3 dyn/cm(2)) or even increased 5-fold under static conditions. This was a result of an enhanced expression of VEGF after reduction of shear stress. Consequently, enhanced podosome formation could be prevented by a VEGF receptor antagonist as well by interruption of VEGF signaling via inhibition of PI3K, Src, or p38. Increase of podosome assembly went along with significantly augmented cell motility. In vivo experiments in mouse arteries confirmed increased endothelial podosome numbers when shear stress was abolished by vessel occlusion. We conclude that shear stress, by reducing VEGF release, inhibits podosome assembly. Hence, endothelial cell-mediated matrix proteolysis and migratory activity are inhibited, thereby stabilizing the structure of the vessel wall.-Fey, T., Schubert, K. M., Schneider, H., Fein, E., Kleinert, E., Pohl, U., Dendorfer, A. Impaired endothelial shear stress induces podosome assembly via VEGF up-regulation.

摘要

足体是具有局部黏附及蛋白水解活性的动态细胞骨架膜结构。它们在血管生成和血管适应性生长中起关键作用。在此,我们在人脐静脉内皮细胞(HUVECs)和小鼠小血管中研究了剪切应力是否控制足体组装和局部蛋白水解活性。通过免疫组织化学对足体进行表征,并将其蛋白水解活性评估为在用作生长底物的荧光明胶中的降解印记。与对照组(10达因/平方厘米)相比,当细胞暴露于低剪切应力(0.3达因/平方厘米)时,每单位时间形成的足体数量增加了一倍,甚至在静态条件下增加了5倍。这是剪切应力降低后血管内皮生长因子(VEGF)表达增强的结果。因此,VEGF受体拮抗剂以及通过抑制磷脂酰肌醇-3-激酶(PI3K)、Src或p38来中断VEGF信号传导,均可防止足体形成增加。足体组装增加伴随着细胞运动性显著增强。在小鼠动脉中进行的体内实验证实,当通过血管闭塞消除剪切应力时,内皮足体数量增加。我们得出结论,剪切应力通过减少VEGF释放来抑制足体组装。因此,内皮细胞介导的基质蛋白水解和迁移活性受到抑制,从而稳定血管壁结构。——费伊,T.,舒伯特,K.M.,施奈德,H.,费恩,E.,克莱纳特,E.,波尔,U.,登多费尔,A. 内皮剪切应力受损通过VEGF上调诱导足体组装。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验