Decisive role of lipopolysaccharide in activating nitric oxide and cytokine production by the probiotic Escherichia coli strain Nissle 1917

被引:0
作者
Z. Zídek
E. Kmoníčková
P. Kostecká
H. Tlaskalová-Hogenová
机构
[1] Academy of Sciences of the Czech Republic,Institute of Experimental Medicine, v.v.i.
[2] Academy of Sciences of the Czech Republic,Institute of Microbiology, v.v.i.
来源
Folia Microbiologica | 2010年 / 55卷
关键词
Nitric Oxide; Nitric Oxide; iNOS mRNA; Peritoneal Cell; Collagenous Colitis;
D O I
暂无
中图分类号
学科分类号
摘要
Effects of Gram-negative probiotic E. coli strain Nissle 1917 (EcN) on the production of nitric oxide (NO) and cytokines were determined in cultures of resident peritoneal cells of rats. The cells (2 × 106/mL) were cultured for 24 h in the presence of live EcN suspension (EcN-Susp), bacteria-free supernatant of this suspension (Sup-EcN), and LPS of EcN origin (LPS-EcN). The biosynthesis of NO was substantially enhanced using live bacteria counts as low as 103/mL applied in the form of EcN-Susp. The same NO-enhancing effect was produced by the correspondingly diluted Sup-EcN. It was found that Sup-EcN contained relatively high amounts of LPS. Administration of the LPS-EcN mimicked the high NO-augmenting activities of both Sup-EcN and EcN-Susp. However, the activity of LPS-EcN was significantly less pronounced than were the activities of Sup-EcN and EcN-Susp containing identical amounts of LPS. The NOstimulatory effects of the EcN preparations were completely inhibited by polymyxin B. All LPS-EcN and correspondingly diluted Sup-EcN and EcN-Susp stimulated the secretion of cytokines TNF-α, IL-1β, IL-6, IL-10 and VEGF. Also these effects were abrogated by polymyxin B. In contrast to the effects on NO production, the cytokine-stimulatory effects were significantly less pronounced after the exposure of the cells to Sup-EcN and EcN-Susp than to the identical amounts of LPS-EcN. It may be concluded that the in vitro stimulatory effects of EcN on NO and cytokine production are mediated by LPS. It is suggested that the immunostimulatory activity of LPS is modulated by EcN-derived factor(s), the nature of which remains to be identified.
引用
收藏
页码:181 / 189
页数:8
相关论文
共 293 条
[1]  
Altenhoefer A.(2004)The probiotic FEMS Immunol.Med.Microbiol. 40 223-229
[2]  
Oswald S.(1991) strain Nissle 1917 interferes with invasion of human intestinal epithelial cells by different enteroinvasive bacterial pathogens J.Exp.Med. 174 1549-1555
[3]  
Sonnenborn U.(1999)Macrophage deactivation by interleukin 10 J.Biomed.Sci. 6 425-432
[4]  
Enders C.(1999)Potentiation of lipopolysaccharide-induced IL-6 release by uridine triphosphate in macrophages: cross-interaction with cyclooxygenase-2-dependent prostaglandin E Mol.Pharmacol. 55 481-488
[5]  
Schulze J.(2001) production J.Immunol. 166 3873-3881
[6]  
Hacker J.(2004)p38 but not p44/42 mitogen-activated protein kinase is required for nitric oxide synthase induction mediated by lipopolysaccharide in RAW 264.7 macrophages FEMS Immunol.Med.Microbiol. 42 173-180
[7]  
Oelschlaeger T.A.(1995)Biphasic regulation of NF-κB activity underlies the pro- and anti-inflammatory actions of nitric oxide Cytokine 7 406-416
[8]  
Bogdan C.(1988)Patterns of cytokine induction by Gram-positive and Gram-negative probiotic bacteria J.Immunol. 141 2407-2412
[9]  
Vodovotz Y.(1998)The modulation of IL-6 and TNF-α release by nitric oxide following stimulation of J774 cells with LPS and IFN-γ Proc.Nat.Acad.Sci.USA 95 126-131
[10]  
Nathan C.(2000)Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production J.Immunol. 165 5245-5254