Cell Biology Program, Hospital for Sick Children, Toronto, Ontario, Canada.
Adv Immunol. 2012;113:7-18. doi: 10.1016/B978-0-12-394590-7.00008-7.
Macrophages are immune cells that participate in the host defense against bacterial pathogens. These cells mediate bacterial clearance by internalizing bacteria into a phagosome, which ultimately fuses with lysosomes to kill bacteria. One bacterial strategy to evade killing in the phagosome is to escape from this compartment prior to lysosomal fusion. Listeria monocytogenes is a classic example of a "cytosol-adapted pathogen" in that it can rapidly escape from the phagosome in macrophages (and other cell types) and replicate rapidly in the cytosol. Phagosome escape also enables cell-to-cell spread by the bacteria through a bacterial driven actin-based motility mechanism. How the bacteria escape the phagosome and evade host cellular defenses, including autophagy, will be discussed in this review. We also discuss an underappreciated population of L. monocytogenes that can replicate in macrophage vacuoles and how these may be important for the establishment of chronic infections.
巨噬细胞是参与宿主防御细菌病原体的免疫细胞。这些细胞通过将细菌内化到吞噬体中来介导细菌清除,吞噬体最终与溶酶体融合以杀死细菌。细菌逃避吞噬体中杀伤的一种策略是在溶酶体融合之前从该隔室逃逸。李斯特菌是一种“胞质适应性病原体”的经典例子,因为它可以在巨噬细胞(和其他细胞类型)中迅速从吞噬体中逃逸,并在胞质中快速复制。吞噬体逃逸还通过细菌驱动的肌动蛋白为基础的运动机制使细菌在细胞间传播。在本综述中,我们将讨论细菌如何从吞噬体逃逸并逃避宿主细胞防御,包括自噬。我们还讨论了可以在巨噬细胞小泡中复制的李斯特菌的一个被低估的群体,以及这些小泡如何对慢性感染的建立很重要。