Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, 225009, People's Republic of China.
In Vitro Cell Dev Biol Anim. 2013 Dec;49(10):778-84. doi: 10.1007/s11626-013-9672-7. Epub 2013 Aug 16.
To explore the responses of host cell after infection with live Salmonella compared with phagocytosis to dead bacteria, the responses of mouse macrophage after infection with Salmonella enteritidis C50041 and the fixed C50041 (C50041-d) were analyzed. Results indicated that the cytotoxicity induced by C50041 was stronger than C50041-d. Similar changing trends of mitochondrial membrane potential, intracellular concentration of calcium ions, reactive oxygen species and nitric oxide were found between C50041 and C50041-d infection. But the cell responses against C50041 were earlier and stronger than C50041-d. LC3 expression of macrophage induced by C50041 was lower than C50041-d. C50041 significantly inhibited the production of tumor necrosis factor and interleukin (IL)-6. Whereas intracellular caspase-1 activation and IL-1β release induced by C50041 were stronger than C50041-d, caspase-1 activation and IL-1β release are the innate defense responses of macrophage. Therefore, it will be beneficial to explore the use of this pathway in the control of Salmonella infection.
为了探究活 Salmonella 感染宿主细胞后的反应与吞噬死菌的反应有何不同,本研究分析了沙门氏菌肠炎亚种 C50041 及其固定株(C50041-d)感染鼠巨噬细胞后的反应。结果表明,C50041 诱导的细胞毒性强于 C50041-d。C50041 与 C50041-d 感染时,线粒体膜电位、细胞内钙离子浓度、活性氧和一氧化氮的变化趋势相似。但是,C50041 引起的细胞反应比 C50041-d 更早、更强。C50041 诱导的巨噬细胞 LC3 表达低于 C50041-d。C50041 显著抑制肿瘤坏死因子和白细胞介素(IL)-6 的产生。然而,C50041 诱导的胞内半胱天冬酶-1 活化和 IL-1β释放强于 C50041-d,半胱天冬酶-1 活化和 IL-1β释放是巨噬细胞的固有防御反应。因此,探索利用这一途径控制 Salmonella 感染将是有益的。