Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Department of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada.
Front Immunol. 2021 Feb 25;12:636078. doi: 10.3389/fimmu.2021.636078. eCollection 2021.
Following phagocytosis, the nascent phagosome undergoes maturation to become a phagolysosome with an acidic, hydrolytic, and often oxidative lumen that can efficiently kill and digest engulfed microbes, cells, and debris. The fusion of phagosomes with lysosomes is a principal driver of phagosomal maturation and is targeted by several adapted intracellular pathogens. Impairment of this process has significant consequences for microbial infection, tissue inflammation, the onset of adaptive immunity, and disease. Given the importance of phagosome-lysosome fusion to phagocyte function and the many virulence factors that target it, it is unsurprising that multiple molecular pathways have evolved to mediate this essential process. While the full range of these pathways has yet to be fully characterized, several pathways involving proteins such as members of the Rab GTPases, tethering factors and SNAREs have been identified. Here, we summarize the current state of knowledge to clarify the ambiguities in the field and construct a more comprehensive phagolysosome formation model. Lastly, we discuss how other cellular pathways help support phagolysosome biogenesis and, consequently, phagocyte function.
吞噬作用发生后,初生吞噬体经历成熟过程,成为具有酸性、水解和通常具有氧化作用的吞噬溶酶体,能够有效杀伤和消化吞噬的微生物、细胞和碎片。吞噬体与溶酶体的融合是吞噬体成熟的主要驱动因素,被几种适应的细胞内病原体靶向。该过程的障碍对微生物感染、组织炎症、适应性免疫的发生和疾病有重大影响。鉴于吞噬体-溶酶体融合对吞噬细胞功能的重要性以及靶向该融合的许多毒力因子,多个分子途径已经进化以介导这一基本过程也就不足为奇了。虽然这些途径的全貌尚未完全确定,但已经确定了几个涉及 Rab GTPases、 tethering factors 和 SNAREs 等蛋白的途径。在这里,我们总结了目前的知识状况,以澄清该领域的模糊性,并构建一个更全面的吞噬溶酶体形成模型。最后,我们讨论了其他细胞途径如何帮助支持吞噬溶酶体的生物发生,从而促进吞噬细胞的功能。