Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Front Cell Infect Microbiol. 2020 Nov 30;10:537782. doi: 10.3389/fcimb.2020.537782. eCollection 2020.
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.
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。