Just I, Fritz G, Aktories K, Giry M, Popoff M R, Boquet P, Hegenbarth S, von Eichel-Streiber C
Institut für Pharmakologie und Toxikologie, Universität des Saarlandes, Homburg-Saar, Germany.
J Biol Chem. 1994 Apr 8;269(14):10706-12.
Clostridium difficile toxin B exhibits cytotoxic activity that is characterized by the disruption of the microfilamental cytoskeleton. Here we studied whether the GTP-binding Rho protein, which reportedly participates in the regulation of the actin cytoskeleton, is involved in the toxin action. Toxin B treatment of Chinese hamster ovary cells reveals a time- and concentration-dependent decrease in the ADP-ribosylation of Rho by Clostridium botulinum C3 exoenzyme in the cell lysate. Disruption of the microfilament system induced by C. botulinum C2 toxin or cytochalasin D does not cause impaired ADP-ribosylation of Rho. Toxin B exhibits its effects on Rho not only in intact cells but also when added to cell lysates. Besides endogenous Rho, RhoA-glutathione S-transferase (Rho-GST) fusion protein added to cell lysate showed decreased ADP-ribosylation after toxin B treatment. Immunoblot analysis reveals identical amounts of Rho-GST and no change in molecular mass after toxin B treatment compared with controls. ADP-ribosylation of Rho-GST purified from toxin B-treated cell lysate is inhibited, indicating a modification of Rho itself. Finally, transfection of rhoA DNA under the control of a strong promoter into cells protects them from the activity of toxin B. Altogether, the data indicate that C. difficile toxin B acts directly or indirectly on Rho proteins to inhibit ADP-ribosylation and suggest that the cytotoxic effect of toxin B involves Rho.
艰难梭菌毒素B具有细胞毒性活性,其特征是微丝细胞骨架的破坏。在这里,我们研究了据报道参与肌动蛋白细胞骨架调节的GTP结合Rho蛋白是否参与毒素作用。用毒素B处理中国仓鼠卵巢细胞后发现,细胞裂解物中肉毒梭菌C3外毒素对Rho的ADP核糖基化作用呈时间和浓度依赖性降低。肉毒梭菌C2毒素或细胞松弛素D诱导的微丝系统破坏不会导致Rho的ADP核糖基化受损。毒素B不仅在完整细胞中对Rho有作用,而且添加到细胞裂解物中时也有作用。除了内源性Rho外,添加到细胞裂解物中的RhoA-谷胱甘肽S-转移酶(Rho-GST)融合蛋白在毒素B处理后显示ADP核糖基化降低。免疫印迹分析显示,与对照相比,毒素B处理后Rho-GST的量相同且分子量没有变化。从毒素B处理的细胞裂解物中纯化的Rho-GST的ADP核糖基化受到抑制,表明Rho本身发生了修饰。最后,将在强启动子控制下的rhoA DNA转染到细胞中可保护它们免受毒素B活性的影响。总之,数据表明艰难梭菌毒素B直接或间接作用于Rho蛋白以抑制ADP核糖基化,并表明毒素B的细胞毒性作用涉及Rho。