Veiga Esteban, Guttman Julian A, Bonazzi Matteo, Boucrot Emmanuel, Toledo-Arana Alejandro, Lin Ann E, Enninga Jost, Pizarro-Cerdá Javier, Finlay B Brett, Kirchhausen Tomas, Cossart Pascale
Institut Pasteur, Unité des Interactions Bactéries-Cellules, Paris F-75015, France.
Cell Host Microbe. 2007 Nov 15;2(5):340-51. doi: 10.1016/j.chom.2007.10.001.
Infection by the bacterium Listeria monocytogenes depends on host cell clathrin. To determine whether this requirement is widespread, we analyzed infection models using diverse bacteria. We demonstrated that bacteria that enter cells following binding to cellular receptors (termed "zippering" bacteria) invade in a clathrin-dependent manner. In contrast, bacteria that inject effector proteins into host cells in order to gain entry (termed "triggering" bacteria) invade in a clathrin-independent manner. Strikingly, enteropathogenic Escherichia coli (EPEC) required clathrin to form actin-rich pedestals in host cells beneath adhering bacteria, even though this pathogen remains extracellular. Furthermore, clathrin accumulation preceded the actin rearrangements necessary for Listeria entry. These data provide evidence for a clathrin-based entry pathway allowing internalization of large objects (bacteria and ligand-coated beads) and used by "zippering" bacteria as part of a general mechanism to invade host mammalian cells. We also revealed a nonendocytic role for clathrin required for extracellular EPEC infections.
单核细胞增生李斯特菌的感染依赖于宿主细胞的网格蛋白。为了确定这种需求是否普遍存在,我们使用多种细菌分析了感染模型。我们证明,与细胞受体结合后进入细胞的细菌(称为“拉链式”细菌)以网格蛋白依赖的方式侵入。相比之下,为了进入宿主细胞而向其中注射效应蛋白的细菌(称为“触发式”细菌)则以网格蛋白非依赖的方式侵入。令人惊讶的是,肠致病性大肠杆菌(EPEC)需要网格蛋白才能在粘附细菌下方的宿主细胞中形成富含肌动蛋白的基座,尽管这种病原体仍位于细胞外。此外,在李斯特菌进入所需的肌动蛋白重排之前,网格蛋白就已经积累。这些数据为基于网格蛋白的进入途径提供了证据,该途径允许内化大型物体(细菌和配体包被的珠子),并且被“拉链式”细菌用作侵入宿主哺乳动物细胞的一般机制的一部分。我们还揭示了网格蛋白在细胞外EPEC感染中所需的非内吞作用。