Hong Jia, Doebele Robert C, Lingen Mark W, Quilliam Lawrence A, Tang Wei-Jen, Rosner Marsha Rich
Ben May Department for Cancer Research, University of Chicago, Chicago, Illinois 60637, USA.
J Biol Chem. 2007 Jul 6;282(27):19781-7. doi: 10.1074/jbc.M700128200. Epub 2007 May 9.
Angiogenesis involves the assembly of endothelial cells into capillaries from a pre-existing vasculature. Because abnormal angiogenesis is a hallmark of many cancers, it is critical to find factors that control this process. Endothelial cells are enriched in the anthrax receptor; we therefore determined the effect of anthrax edema toxin (ET), an adenylyl cyclase, on chemotaxis. cAMP generated by ET does not block proliferation or survival but causes cytoskeletal changes and inhibits chemotaxis by primary human microvascular endothelial cells (HMVECs). These effects are due to the action of a downstream cAMP effector, Epac, a guanine nucleotide exchange-activating protein for Rap1 (RAP1-GEF). ET induces transcription of Epac-related activators of Rap1, Epac2 (RapGEF4), and MR-GEF/RapGEF5. Similar to ET, activated Epac or Rap1 induces cytoskeletal changes and blocks chemotaxis in human endothelial cells. These results identify Epac and Rap1 as key regulators of signaling cascades leading to endothelial cell chemotaxis.
血管生成涉及内皮细胞从预先存在的脉管系统组装成毛细血管。由于异常血管生成是许多癌症的一个标志,因此找到控制这一过程的因素至关重要。内皮细胞富含炭疽受体;因此,我们确定了腺苷酸环化酶炭疽水肿毒素(ET)对趋化性的影响。ET产生的cAMP不会阻断增殖或存活,但会引起细胞骨架变化并抑制原代人微血管内皮细胞(HMVECs)的趋化性。这些作用归因于下游cAMP效应器Epac(一种Rap1的鸟嘌呤核苷酸交换激活蛋白,即RAP1-GEF)的作用。ET诱导Epac相关的Rap1激活剂Epac2(RapGEF4)和MR-GEF/RapGEF5的转录。与ET相似,激活的Epac或Rap1会诱导细胞骨架变化并阻断人内皮细胞的趋化性。这些结果确定Epac和Rap1是导致内皮细胞趋化性的信号级联反应的关键调节因子。