Larabee Jason L, DeGiusti Kevin, Regens James L, Ballard Jimmy D
Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Infect Immun. 2008 Nov;76(11):4895-904. doi: 10.1128/IAI.00889-08. Epub 2008 Sep 2.
Bacillus anthracis edema toxin (ET) generates high levels of cyclic AMP and impacts a complex network of signaling pathways in targeted cells. In the current study, we sought to identify kinase signaling pathways modulated by ET to better understand how this toxin alters cell physiology. Using a panel of small-molecule inhibitors of mammalian kinases, we found that inhibitors of glycogen synthase kinase 3 beta (GSK-3beta) protected cells from ET-induced changes in the cell cycle. GSK-3beta inhibitors prevented declines in cellular levels of cyclin D1 and c-Jun following treatment of macrophages with ET. Strikingly, cell fractionation experiments and confocal immunofluorescence microscopy revealed that ET activates a compartmentalized pool of GSK-3beta residing in the nuclei, but not in the cytoplasm, of macrophages. To investigate the outcome of this event, we examined the cellular location and activation state of beta-catenin, a critical substrate of GSK-3beta, and found that the protein was inactivated within the nucleus following intoxication with ET. To determine if ET could overcome the effects of stimuli that inactivate GSK-3beta, we examined the impact of the toxin on the Wnt signaling pathway. The results of these experiments revealed that by targeting GSK-3beta residing in the nucleus, ET circumvents the upstream cytoplasmic inactivation of GSK-3beta, which occurs following exposure to Wnt-3A. These findings suggest ET arrests the cell cycle by a mechanism involving activation of GSK-3beta residing in the nucleus, and by using this novel mechanism of intoxication, ET avoids cellular systems that would otherwise reverse the effects of the toxin.
炭疽芽孢杆菌水肿毒素(ET)可产生高水平的环磷酸腺苷(cAMP),并影响靶细胞中复杂的信号通路网络。在本研究中,我们试图确定受ET调节的激酶信号通路,以更好地理解这种毒素如何改变细胞生理学。使用一组哺乳动物激酶的小分子抑制剂,我们发现糖原合酶激酶3β(GSK-3β)抑制剂可保护细胞免受ET诱导的细胞周期变化的影响。用ET处理巨噬细胞后,GSK-3β抑制剂可防止细胞周期蛋白D1和c-Jun的细胞水平下降。引人注目的是,细胞分级分离实验和共聚焦免疫荧光显微镜显示,ET激活了巨噬细胞核内而非细胞质中的GSK-3β分隔池。为了研究这一事件的结果,我们检查了GSK-3β的关键底物β-连环蛋白的细胞定位和激活状态,发现ET中毒后该蛋白在细胞核内失活。为了确定ET是否能克服使GSK-3β失活的刺激的影响,我们检查了毒素对Wnt信号通路的影响。这些实验结果表明,通过靶向细胞核内的GSK-3β,ET规避了暴露于Wnt-3A后发生的GSK-3β上游细胞质失活。这些发现表明,ET通过一种涉及激活细胞核内GSK-3β的机制使细胞周期停滞,并且通过这种新的中毒机制,ET避开了否则会逆转毒素作用的细胞系统。