Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Exp Cell Res. 2010 Jul 15;316(12):1946-57. doi: 10.1016/j.yexcr.2010.03.026. Epub 2010 Apr 9.
Mechanisms for receptor-mediated anthrax toxin internalization and delivery to the cytosol are well understood. However, far less is known about the fate followed by anthrax toxin receptors prior and after cell exposure to the toxin. We report that Anthrax Toxin Receptor 1/Tumor Endothelial Marker 8 (TEM8) localized at steady state in Rab11a-positive and transferrin receptor-containing recycling endosomes. TEM8 followed a slow constitutive recycling route of approximately 30min as determined by pulsed surface biotinylation and chase experiments. A Rab11a dominant negative mutant and Myosin Vb tail expression impaired TEM8 recycling by sequestering TEM8 in intracellular compartments. Sequestration of TEM8 in intracellular compartments with monensin coincided with increased TEM8 association with a multi-protein complex isolated with antibodies against transferrin receptor. Addition of the cell-binding component of anthrax toxin, Protective Antigen, reduced TEM8 half-life from 7 to 3 hours, without preventing receptor recycling. Pharmacological and molecular perturbation of recycling endosome function using monensin, dominant negative Rab11a, or myosin Vb tail, reduced PA binding efficiency and TEM8-dependent cell spreading on PA-coated surfaces without affecting toxin delivery to the cytosol. These results indicate that the intracellular fate of TEM8 differentially affect its cell adhesion and cell intoxication functions.
受体介导的炭疽毒素内化和胞浆内递呈的机制已得到充分理解。然而,对于炭疽毒素受体在细胞暴露于毒素前后的命运,人们知之甚少。我们报告称,炭疽毒素受体 1/肿瘤内皮标志物 8(TEM8)在稳态时定位于 Rab11a 阳性和转铁蛋白受体含有再循环内体中。通过脉冲表面生物素标记和追踪实验,TEM8 遵循一条缓慢的组成性再循环途径,约 30 分钟。Rab11a 显性负突变体和肌球蛋白 Vb 尾部表达通过将 TEM8 隔离在内质体中,损害了 TEM8 的再循环。用莫能菌素将 TEM8 隔离在内质体中,与用转铁蛋白受体抗体分离的多蛋白复合物增加了 TEM8 的关联。炭疽毒素的细胞结合成分保护抗原的添加将 TEM8 的半衰期从 7 小时缩短至 3 小时,而不会阻止受体再循环。使用莫能菌素、显性负 Rab11a 或肌球蛋白 Vb 尾部对再循环内体功能进行药理学和分子干扰,降低了 PA 结合效率和 TEM8 依赖性细胞在 PA 涂层表面上的铺展,而不影响毒素向胞浆内的递呈。这些结果表明,TEM8 的细胞内命运会对其细胞黏附和细胞中毒功能产生不同的影响。