Department of Biological Sciences, University of Toronto at Scarborough, Toronto, Ontario, Canada.
Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.
J Cell Biol. 2021 Sep 6;220(9). doi: 10.1083/jcb.202005072. Epub 2021 Jun 28.
Phagocytes engulf unwanted particles into phagosomes that then fuse with lysosomes to degrade the enclosed particles. Ultimately, phagosomes must be recycled to help recover membrane resources that were consumed during phagocytosis and phagosome maturation, a process referred to as "phagosome resolution." Little is known about phagosome resolution, which may proceed through exocytosis or membrane fission. Here, we show that bacteria-containing phagolysosomes in macrophages undergo fragmentation through vesicle budding, tubulation, and constriction. Phagosome fragmentation requires cargo degradation, the actin and microtubule cytoskeletons, and clathrin. We provide evidence that lysosome reformation occurs during phagosome resolution since the majority of phagosome-derived vesicles displayed lysosomal properties. Importantly, we show that clathrin-dependent phagosome resolution is important to maintain the degradative capacity of macrophages challenged with two waves of phagocytosis. Overall, our work suggests that phagosome resolution contributes to lysosome recovery and to maintaining the degradative power of macrophages to handle multiple waves of phagocytosis.
吞噬细胞将不需要的颗粒吞噬到吞噬体中,然后吞噬体与溶酶体融合,降解包裹的颗粒。最终,吞噬体必须被回收,以帮助恢复吞噬作用和吞噬体成熟过程中消耗的膜资源,这个过程被称为“吞噬体解体”。目前对于吞噬体解体知之甚少,它可能通过胞吐或膜分裂进行。在这里,我们发现巨噬细胞中的含菌吞噬溶酶体通过囊泡出芽、管状化和收缩而发生碎片化。吞噬体碎片化需要货物降解、肌动蛋白和微管细胞骨架以及网格蛋白。我们提供的证据表明,溶酶体的再形成发生在吞噬体解体过程中,因为大多数吞噬体衍生的囊泡显示出溶酶体特性。重要的是,我们表明,网格蛋白依赖性吞噬体解体对于维持受到两波吞噬作用挑战的巨噬细胞的降解能力很重要。总的来说,我们的工作表明,吞噬体解体有助于溶酶体的恢复,并维持巨噬细胞降解能力以应对多波吞噬作用。