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Dysregulated endolysosomal trafficking in cells arrested in the G1 phase of the host cell cycle impairs Salmonella vacuolar replication

机译:在宿主细胞周期的 G1 期停滞的细胞中内溶酶体运输失调会损害沙门氏菌空泡复制

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摘要

Modulation of the host cell cycle has emerged as a common theme among the pathways regulated by bacterial pathogens, arguably to promote host cell colonization. However, in most cases the exact benefit ensuing from such interference to the infection process remains unclear. Previously, we have shown that Salmonella actively induces G2/M arrest of host cells, and that infection is severely inhibited in cells arrested in G1. In this study, we demonstrate that Salmonella vacuolar replication is inhibited in host cells blocked in G1, whereas the cytosolic replication of the closely related pathogen Shigella is not affected. Mechanistically, we show that cells arrested in G1, but not cells arrested in G2, present dysregulated endolysosomal trafficking, displaying an abnormal accumulation of vesicles positive for late endosomal and lysosomal markers. In addition, the macroautophagic/autophagic flux and degradative lysosomal function are strongly impaired. This endolysosomal trafficking dysregulation results in sustained activation of the SPI-1 type III secretion system and lack of vacuole repair by the autophagy pathway, ultimately compromising the maturation and integrity of the Salmonella-containing vacuole. As such, Salmonella is released in the host cytosol. Collectively, our findings demonstrate that the modulation of the host cell cycle occurring during Salmonella infection is related to a disparity in the permissivity of cells arrested in G1 and G2/M, due to their intrinsic characteristics.Abbreviations: CDK4: cyclin dependent kinase 4; CDK6: cyclin dependent kinase 6; CDK4-CDK6i: CDK4-CDK6 inhibitor IV; cfu: colony-forming units; CHQ: chloroquine; DMSO: dimethyl sulfoxide; EEA1: early endosome antigen 1; FITC: fluorescein isothiocyanate; GFP: green fluorescent protein; hpi: hours post-infection; LAMP1: lysosomal associated membrane protein 1; MAP1LC3B/LC3B: microtubule associated protein 1 light chain 3 beta; MOI: multiplicity of infection; RAB7: RAB7, member RAS oncogene family; SCV: Salmonella-containing vacuole; SPI-1: Salmonella pathogenicity island-1; SPI-2: Salmonella pathogenicity island-2; TFEB: transcription factor EB; T3SS: type III secretion system
机译:宿主细胞周期的调节已成为细菌病原体调节的途径中的一个共同主题,可以说是促进宿主细胞定植。然而,在大多数情况下,这种干扰对感染过程的确切好处仍不清楚。以前,我们已经表明沙门氏菌积极诱导宿主细胞的 G2/M 期阻滞,并且在 G1 期阻滞的细胞中感染受到严重抑制。在这项研究中,我们证明沙门氏菌液泡复制在 G1 被阻断的宿主细胞中受到抑制,而密切相关的病原体志贺氏菌的胞质复制不受影响。从机制上讲,我们表明在 G1 中停滞的细胞,而不是在 G2 中停滞的细胞,表现为内溶酶体运输失调,显示晚期内体和溶酶体标志物阳性的囊泡异常积累。此外,巨自噬/自噬通量和降解溶酶体功能严重受损。这种内溶酶体运输失调导致 SPI-1 III 型分泌系统持续激活和自噬途径缺乏液泡修复,最终损害含沙门氏菌液泡的成熟和完整性。因此,沙门氏菌在宿主胞质溶胶中释放。总的来说,我们的研究结果表明,由于它们的内在特性,沙门氏菌感染期间发生的宿主细胞周期的调节与在 G1 和 G2/M 中停滞的细胞的允许性差异有关。缩写: CDK4: 细胞周期蛋白依赖性激酶 4;CDK6: 细胞周期蛋白依赖性激酶 6;CDK4-CDK6i: CDK4-CDK6 抑制剂 IV;CFU: 菌落形成单位;CHQ: 氯喹;DMSO: 二甲基亚砜;EEA1: 早期内体抗原 1;FITC: 异硫氰酸荧光素;GFP: 绿色荧光蛋白;HPI:感染后小时数;LAMP1: 溶酶体相关膜蛋白 1;MAP1LC3B/LC3B: 微管相关蛋白 1 轻链 3 β;MOI: 感染复数;RAB7: RAB7,RAS 癌基因家族成员;SCV: 含沙门氏菌液泡;SPI-1: 沙门氏菌致病性岛-1;SPI-2: 沙门氏菌致病性岛-2;TFEB: 转录因子 EB;T3SS:III 型分泌系统

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