Tran Van Nhieu G, Ben-Ze'ev A, Sansonetti P J
Unité de Pathogénie Microbienne Moléculaire, INSERM U389, Institut Pasteur, Paris, France.
EMBO J. 1997 May 15;16(10):2717-29. doi: 10.1093/emboj/16.10.2717.
Shigella flexneri is the causative agent of bacillary dysentery in humans. Shigella invasion of epithelial cells is characterized by cytoskeletal rearrangements and formation of cellular projections engulfing the bacterium in a macropinocytic process. We show here that vinculin, a protein involved in linking actin filaments to the plasma membrane, is a direct target of Shigella during cell invasion. IpaA, a Shigella protein secreted upon cell contact, rapidly associates with vinculin during bacterial invasion. Although defective for cell entry, an ipaA mutant is still able to induce foci of actin polymerization, but differs from wild-type Shigella in its ability to recruit vinculin and alpha-actinin. Presumably, IpaA-vinculin interaction initiates the formation of focal adhesion-like structures required for efficient invasion.
福氏志贺菌是人类细菌性痢疾的病原体。志贺菌对上皮细胞的侵袭以细胞骨架重排和形成细胞突起为特征,这些细胞突起通过巨吞饮过程吞噬细菌。我们在此表明,纽蛋白(一种参与将肌动蛋白丝连接到质膜的蛋白质)是志贺菌在细胞侵袭过程中的直接靶点。IpaA是志贺菌在细胞接触时分泌的一种蛋白质,在细菌侵袭期间迅速与纽蛋白结合。尽管ipaA突变体在细胞进入方面存在缺陷,但它仍然能够诱导肌动蛋白聚合灶,但其招募纽蛋白和α - 辅肌动蛋白的能力与野生型志贺菌不同。据推测,IpaA - 纽蛋白相互作用启动了有效侵袭所需的黏着斑样结构的形成。