Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Cologne, Germany.
Center of Molecular Medicine Cologne, Cologne, Germany.
Autophagy. 2022 May;18(5):1090-1107. doi: 10.1080/15548627.2021.1969765. Epub 2021 Sep 5.
Non-canonical autophagy pathways decorate single-membrane vesicles with Atg8-family proteins such as MAP1LC3/LC3 (microtubule-associated protein 1 light chain 3). Phagosomes containing the bacterial pathogen (L.m.) can be targeted by a non-canonical autophagy pathway called LC3-associated phagocytosis (LAP), which substantially contributes to the anti-listerial activity of macrophages and immunity. We here characterized a second non-canonical autophagy pathway targeting L.m.-containing phagosomes, which is induced by damage caused to the phagosomal membrane by the pore-forming toxin of L.m., listeriolysin O. This pore-forming toxin-induced non-canonical autophagy pathway (PINCA) was the only autophagic pathway evoked in tissue macrophages deficient for the NADPH oxidase CYBB/NOX2 that produces the reactive oxygen species (ROS) that are required for LAP induction. Similarly, also bone marrow-derived macrophages (BMDM) exclusively targeted L.m. by PINCA as they completely failed to induce LAP because of insufficient production of ROS through CYBB, in part, due to low expression of some CYBB complex subunits. Priming of BMDM with proinflammatory cytokines such as TNF and IFNG/IFNγ increased ROS production by CYBB and endowed them with the ability to target L.m. by LAP. Targeting of L.m. by LAP remained relatively rare, though, preventing LAP from substantially contributing to the anti-listerial activity of BMDM. Similar to LAP, the targeting of L.m.-containing phagosomes by PINCA promoted their fusion with lysosomes. Surprisingly, however, this did not substantially contribute to anti-listerial activity of BMDM. Thus, in contrast to LAP, PINCA does not have clear anti-listerial function suggesting that the two different non-canonical autophagy pathways targeting L.m. may have discrete functions.: actA/ActA: actin assembly-inducing protein A; ATG: autophagy-related; BMDM: Bone marrow-derived macrophages; CALCOCO2/NDP52: calcium-binding and coiled-coil domain-containing protein 2; CYBA/p22phox: cytochrome b-245 light chain; CYBB/NOX2: cytochrome b(558) subunit beta; ; IFNG/IFNγ: interferon gamma; L.m.: ; LAP: LC3-associated phagocytosis; LGALS: galectin; LLO: listeriolysin O; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; NCF1/p47phox: neutrophil cytosol factor 1; NCF2/p67phox: neutrophil cytosol factor 2; NCF4/p67phox: neutrophil cytosol factor 4; Peritoneal macrophages: PM; PINCA: pore-forming toxin-induced non-canonical autophagy; plc/PLC: 1-phosphatidylinositol phosphodiesterase; PMA: phorbol 12-myristate 13-acetate; RB1CC1/FIP200: RB1-inducible coiled-coil protein 1; ROS: reactive oxygen species; ; SQSTM1/p62: sequestosome 1; ; T3SS: type III secretion system; TNF: tumor necrosis factor; ULK: unc-51 like autophagy activating kinase; PM: peritoneal macrophages; WT: wild type.
非典型自噬途径会用 MAP1LC3/LC3(微管相关蛋白 1 轻链 3)等 Atg8 家族蛋白对单膜囊泡进行修饰。含有细菌病原体 (L.m.)的吞噬体可以被一种称为 LC3 相关吞噬作用(LAP)的非典型自噬途径靶向,该途径对巨噬细胞的抗李斯特菌活性和免疫有很大贡献。我们在这里描述了第二种靶向含有 L.m.的吞噬体的非典型自噬途径,该途径由 L.m.的穿孔毒素——李斯特菌溶血素 O 对吞噬体膜造成的损伤诱导。这种由穿孔毒素诱导的非典型自噬途径(PINCA)是唯一在 NADPH 氧化酶 CYBB/NOX2 缺失的组织巨噬细胞中被诱发的自噬途径,该酶产生的活性氧(ROS)是 LAP 诱导所必需的。同样,骨髓来源的巨噬细胞(BMDM)也仅通过 PINCA 靶向 L.m.,因为它们由于 CYBB 产生的 ROS 不足,完全无法诱导 LAP,部分原因是一些 CYBB 复合物亚基的表达水平较低。通过 TNF 和 IFNG/IFNγ 等促炎细胞因子对 BMDM 进行预处理,增加了 CYBB 产生的 ROS,使它们能够通过 LAP 靶向 L.m.。然而,尽管 LAP 靶向 L.m.的频率相对较低,但这并不能显著促进 BMDM 的抗李斯特菌活性。与 LAP 类似,PINCA 也促进了含有 L.m.的吞噬体与溶酶体的融合。令人惊讶的是,这并没有显著促进 BMDM 的抗李斯特菌活性。因此,与 LAP 不同,PINCA 没有明显的抗李斯特菌功能,这表明靶向 L.m.的两种不同的非典型自噬途径可能具有不同的功能。