de Bernard M, Burroni D, Papini E, Rappuoli R, Telford J, Montecucco C
Centro CNR Biomembrane and Dipartimento di Scienze Biomediche, Università di Padova, 35121 Padova, Italy.
Infect Immun. 1998 Dec;66(12):6014-6. doi: 10.1128/IAI.66.12.6014-6016.1998.
Cells exposed to Helicobacter pylori toxin VacA develop large vacuoles which originate from massive swelling of membranous compartments at late stages of the endocytic pathway. When expressed in the cytosol, VacA induces vacuolization as it does when added from outside. This and other evidence indicate that VacA is a toxin capable of entering the cell cytosol, where it displays its activity. In this study, we have used cytosolic expression to identify the portion of the toxin molecule responsible for the vacuolating activity. VacA mutants with deletions at the C and N termini were generated, and their activity was analyzed upon expression in HeLa cells. We found that the vacuolating activity of VacA resides in the amino-terminal region, the whole of which is required for its intracellular activity.
暴露于幽门螺杆菌毒素VacA的细胞会形成大液泡,这些液泡源自内吞途径后期膜性区室的大量肿胀。当在细胞质中表达时,VacA诱导形成液泡,就像从外部添加时一样。这一现象及其他证据表明,VacA是一种能够进入细胞质并在其中发挥活性的毒素。在本研究中,我们利用细胞质表达来确定毒素分子中负责空泡化活性的部分。构建了C端和N端缺失的VacA突变体,并在HeLa细胞中表达后分析其活性。我们发现VacA的空泡化活性位于氨基末端区域,其整个区域对于细胞内活性都是必需的。