School of Science and Technology, Life Science, Örebro University, Sweden.
BMC Microbiol. 2012 Jan 22;12:15. doi: 10.1186/1471-2180-12-15.
Epithelial cells of the urinary tract recognize pathogenic bacteria through pattern recognition receptors on their surface, such as toll-like receptors (TLRs), and mount an immune response through the activation of the NF-kappaB pathway. Some uropathogenic bacteria can subvert these cellular responses, creating problems with how the host eliminates pathogens. Lactobacillus is a genus of lactic acid bacteria that are part of the microbiota and consist of many probiotic strains, some specifically for urogenital infections. Immunomodulation has emerged as an important mode of action of probiotic and commensal lactobacilli and given the importance of epithelial cells, we evaluated the effect of the urogenital probiotic Lactobacillus rhamnosus GR-1 on epithelial immune activation.
Immune activation through the NF-kappaB pathway was initiated by stimulation of T24 urothelial cells with heat-killed Escherichia coli and this was further potentiated when cells were co-cultured with live L. rhamnosus GR-1. Heat-killed lactobacilli were poor activators of NF-kappaB. Concomitant stimulation of bladder cells with E. coli and L. rhamnosus GR-1 increased the levels of the pro-inflammatory cytokine TNF, whereas IL-6 and CXCL8 levels were reduced. Another probiotic, L. rhamnosus GG, was also able to potentiate NF-kappaB in these cells although at a significantly reduced level compared to the GR-1 strain. The transcript numbers and protein levels of the lipopolysaccharide receptor TLR4 were significantly increased after co-stimulation with E. coli and lactobacilli compared to controls. Furthermore, inhibition of TLR4 activation by polymixin B completely blocked the lactobacilli potentiation of NF-kappaB.
The immunological outcome of E. coli challenge of bladder cells was influenced by probiotic L. rhamnosus GR-1, by enhancing the activation of NF-kappaB and TNF release. Thus the urogenital probiotic L. rhamnosus GR-1 modulated the activation of the NF-kappaB through increased levels of TLR4 on the bladder cells and altered subsequent release of cytokines from urothelial cells. By influencing immunological factors such as TLR4, important in the process of fighting pathogens, lactobacilli could facilitate pathogen recognition and infection clearance.
尿路上皮细胞通过表面的模式识别受体(如 toll 样受体(TLR))识别致病细菌,并通过 NF-kappaB 途径的激活来启动免疫反应。一些尿路致病性细菌可以颠覆这些细胞反应,导致宿主清除病原体出现问题。乳杆菌是乳酸杆菌属的一种,是微生物群的一部分,由许多益生菌株组成,有些专门用于泌尿生殖系统感染。免疫调节已成为益生菌和共生乳杆菌的重要作用模式,鉴于上皮细胞的重要性,我们评估了泌尿生殖益生菌乳杆菌 rhamnosus GR-1 对上皮免疫激活的影响。
用热灭活大肠杆菌刺激 T24 尿路上皮细胞可引发 NF-kappaB 途径的免疫激活,当细胞与活的乳杆菌 rhamnosus GR-1 共培养时,这种激活作用进一步增强。热灭活的乳杆菌对 NF-kappaB 的激活作用较差。膀胱细胞同时用大肠杆菌和乳杆菌 rhamnosus GR-1 刺激可增加促炎细胞因子 TNF 的水平,而 IL-6 和 CXCL8 的水平降低。另一种益生菌乳杆菌 rhamnosus GG 也能增强这些细胞中的 NF-kappaB,但与 GR-1 株相比,其作用明显降低。与对照组相比,大肠杆菌和乳杆菌共刺激后,TLR4 的转录数和蛋白水平显著增加。此外,多粘菌素 B 抑制 TLR4 激活完全阻断了乳杆菌对 NF-kappaB 的增强作用。
与对照相比,膀胱细胞大肠杆菌挑战的免疫学结果受益生菌乳杆菌 rhamnosus GR-1 的影响,通过增强 NF-kappaB 和 TNF 释放来增强其激活。因此,泌尿生殖益生菌乳杆菌 rhamnosus GR-1 通过增加膀胱细胞上 TLR4 的水平来调节 NF-kappaB 的激活,并改变尿路上皮细胞随后释放细胞因子。通过影响 TLR4 等免疫因素,乳杆菌有助于病原体的识别和感染清除,在对抗病原体的过程中发挥重要作用。