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鼠伤寒血清型沙门氏菌在 RAW264.7 吞噬细胞中的复制与缺氧和缺乏诱导型一氧化氮合酶表达相关。

Replication of serovar Typhimurium in RAW264.7 Phagocytes Correlates With Hypoxia and Lack of iNOS Expression.

机构信息

Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.

Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

Front Cell Infect Microbiol. 2020 Nov 30;10:537782. doi: 10.3389/fcimb.2020.537782. eCollection 2020.

Abstract

infection associates with tissue hypoxia, while inducible nitric oxide synthase (iNOS), relying for its activity on molecular oxygen, stands as a central host defence measure in murine salmonellosis. Here, we have detailed hypoxia and iNOS responses of murine macrophage-like RAW264.7 cells upon infection with serovar Typhimurium. We noted that only a proportion of the infected RAW264.7 cells became hypoxic or expressed iNOS. Heavily infected cells became hypoxic, while in parallel such cells tended not to express iNOS. While a proportion of the infected RAW264.7 cells revealed shutdown of protein synthesis, this was only detectable after 12 h post infection and after iNOS expression was induced in the cell culture. Our data implicate an intrinsic heterogeneity with regard to hypoxia and iNOS expression in a cell culture-based infection setting.

摘要

感染与组织缺氧有关,而诱导型一氧化氮合酶(iNOS)依赖于分子氧发挥其活性,是鼠伤寒沙门氏菌病中宿主防御的重要措施。在这里,我们详细研究了鼠源巨噬细胞样 RAW264.7 细胞感染血清型鼠伤寒沙门氏菌后的缺氧和 iNOS 反应。我们注意到,只有一部分感染的 RAW264.7 细胞会出现缺氧或表达 iNOS。严重感染的细胞会出现缺氧,而同时这些细胞往往不会表达 iNOS。虽然一部分感染的 RAW264.7 细胞的蛋白质合成被关闭,但这仅在感染后 12 小时后才能检测到,并且在细胞培养中诱导 iNOS 表达之后。我们的数据表明,在基于细胞培养的感染环境中,缺氧和 iNOS 表达存在内在异质性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a94/7734562/800480ada8ec/fcimb-10-537782-g001.jpg

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