IL-10 produced by trophoblast cells inhibits phagosome maturation leading to profound intracellular proliferation of Salmonella enterica Typhimurium

被引:19
|
作者
Nguyen, T. [1 ,2 ]
Robinson, N. [1 ]
Allison, S. E. [3 ]
Coombes, B. K. [3 ]
Sad, S. [1 ,2 ]
Krishnan, L. [1 ,2 ]
机构
[1] Univ Ottawa, Fac Med, Dept Biochem Microbiol & Immunol, Ottawa, ON K1N 6N5, Canada
[2] Natl Res Council Canada, Div Life Sci, Ottawa, ON K4A 0R6, Canada
[3] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON L8N 3Z5, Canada
基金
加拿大健康研究院;
关键词
Trophoblast cells; Salmonella Typhimurium; Pregnancy; Interleukin; 10; Phagosomal maturation; Immune response; TOLL-LIKE RECEPTORS; SEROVAR TYPHIMURIUM; SCAVENGER RECEPTOR; IFN-GAMMA; INFLAMMATION; INFECTION; PREGNANCY; INTERLEUKIN-10; SUSCEPTIBILITY; TRANSMISSION;
D O I
10.1016/j.placenta.2013.06.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Salmonella enterica Typhimurium (ST) is a phagosomal pathogen that can infect placental trophoblast cells leading to abortion and severe maternal illness. It is unclear how the trophoblast cells promote profound bacterial proliferation. Methods: The mechanism of internalization, intracellular growth and phagosomal biogenesis in ST-infected human epithelial (HeLa), macrophage (THP-1) and trophoblast-derived cell lines (JEG-3, BeWo and HTR-8) was studied. Specific inhibitors were used to block bacterial internalization. Phagosomal maturation was determined by confocal microscopy, Western-blotting and release of lysosomal beta-galactosidase by infected cells. Bacterial colony forming units were determined by plating infected cell lysates on agar plates. Results: ST proliferated minimally in macrophages but replicated profoundly within trophoblast cells. The ST-Delta invA (a mutant of Salmonella pathogenicity island-1 gene effector proteins) was unable to infect epithelial cells, but was internalized by scavenger receptors on trophoblasts and macrophages. However, ST was contrastingly localized in early (Rab5(+)) or late (LAMP1(+)) phagosomes within trophoblast cells and macrophages respectively. Furthermore trophoblast cells (unlike macrophages) did not exhibit phagoso-lysosomal fusion. ST-infected macrophages produced IL-6 whereas trophoblast cells produced IL-10. Neutralizing IL-10 in JEG-3 cells accelerated phagolysomal fusion and reduced proliferation of ST. Placental bacterial burden was curtailed in vivo in anti-IL-10 antibody treated and IL-10-deficient mice. Discussion: Macrophages phagocytose but curtail intracellular replication of ST in late phagosomes. In contrast, phagocytosis by trophoblast cells results in an inappropriate cytokine response and proliferation of ST in early phagosomes. Conclusion: IL-10 production by trophoblast cells that delays phagosomal maturation may facilitate proliferation of pathogens in placental cells. Crown Copyright (C) 2013 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:765 / 774
页数:10
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