Vojtová Jana, Kofronová Olga, Sebo Peter, Benada Oldrich
Institute of Microbiology, Academy of Sciences of the Czech Republic, 142 20, Prague 4, Czech Republic.
Microsc Res Tech. 2006 Feb;69(2):119-29. doi: 10.1002/jemt.20277.
Adenylate cyclase toxin (CyaA) of Bordetella pertussis penetrates the membrane of eukaryotic cells, producing high levels of intracellular cAMP, as well as hemolysis that results from the formation of cation-selective toxin channels in the membrane. Using several microscopical approaches we studied the effects of CyaA action on the morphology of sheep erythrocytes during early phases preceding lysis and examined localization of CyaA molecules within the erythrocyte membrane. CyaA induced a cascade of morphological changes of erythrocytes, such as shrinkage, formation of membrane projections, and blebs and swelling. The use of an enzymatically inactive CyaA-AC- toxoid that is unable to produce cAMP and of a CyaA-E581K mutant exhibiting higher hemolytic activity than with CyaA showed that the hemolytic activity is responsible for the induction of morphological changes of erythrocytes. Further, immunolabeling of inserted CyaA-232/FLAG molecules with specific anti-FLAG antibodies and IgG-gold particles indicated a clustered distribution of CyaA molecules in erythrocyte membrane. This was confirmed by immunofluorescence and confocal microscopy, which revealed uniform stoichiometry of CyaA clusters, suggesting CyaA binding into specific domains in erythrocyte membrane. Indeed, a decrease of CyaA binding after cholesterol depletion of erythrocytes suggests toxin targeting and binding to membrane microdomains (rafts).
百日咳博德特氏菌的腺苷酸环化酶毒素(CyaA)可穿透真核细胞的膜,产生高水平的细胞内cAMP,以及因膜中阳离子选择性毒素通道形成而导致的溶血现象。我们使用多种显微镜方法研究了CyaA作用在溶血前期对绵羊红细胞形态的影响,并检测了CyaA分子在红细胞膜内的定位。CyaA诱导了红细胞一系列的形态变化,如收缩、膜突起形成、泡状结构和肿胀。使用无法产生cAMP的无酶活性的CyaA-AC类毒素以及溶血活性高于CyaA的CyaA-E581K突变体,结果表明溶血活性是诱导红细胞形态变化的原因。此外,用特异性抗FLAG抗体和IgG-金颗粒对插入的CyaA-232/FLAG分子进行免疫标记,结果表明CyaA分子在红细胞膜中呈簇状分布。免疫荧光和共聚焦显微镜证实了这一点,其显示CyaA簇具有均匀的化学计量比,表明CyaA结合到红细胞膜中的特定结构域。事实上,红细胞胆固醇耗竭后CyaA结合减少,提示毒素靶向并结合到膜微结构域(脂筏)。