Bäckhed F, Söderhäll M, Ekman P, Normark S, Richter-Dahlfors A
Microbiology and Tumour Biology Center, Karolinska Institutet, Stockholm, Sweden.
Cell Microbiol. 2001 Mar;3(3):153-8. doi: 10.1046/j.1462-5822.2001.00101.x.
Mucosal epithelial linings function as physical barriers against microbes. In addition, they participate in the first line of host defence by production of a variety of proinflammatory mediators when exposed to microbes and microbial agents. Here, we use a human urinary tract infection model to demonstrate that organ- and cell-specific innate responses induced by lipopolysaccharides (LPS) present on Gram-negative bacteria correlates with the expression of Toll-like receptor 4 (TLR4). The presence of TLR4 on human bladder epithelial cells enables them to rapidly respond to bacterial infections in vitro and in vivo. In contrast, TLR4 is not expressed on human proximal tubule cells isolated from the renal cortex, which may explain the cortical localization of bacteria in pyelonephritis. TLR4-negative renal epithelial cells, A498, are non-responsive to purified LPS, however, they respond to viable bacteria via a mannose-sensitive attachment-mediated pathway. To identify LPS components recognised by bladder epithelial cells, a bacterial lipid A mutant and LPS of different chemotypes were tested. Full interleukin 8 induction required hexa-acylated lipid A and was decreased by between 50% and 70% in the presence of O-antigen. Taken together, we propose that multiple independent pathways, which are organ- and cell-specifically expressed, mediate bacterial recognition and determine the outcome of innate responses to infection.
黏膜上皮衬里作为抵御微生物的物理屏障。此外,当暴露于微生物和微生物制剂时,它们通过产生多种促炎介质参与宿主防御的第一线。在这里,我们使用人类尿路感染模型来证明革兰氏阴性菌上存在的脂多糖(LPS)诱导的器官和细胞特异性先天反应与Toll样受体4(TLR4)的表达相关。人类膀胱上皮细胞上TLR4的存在使它们能够在体外和体内快速响应细菌感染。相比之下,从肾皮质分离的人类近端小管细胞上不表达TLR4,这可能解释了肾盂肾炎中细菌的皮质定位。TLR4阴性的肾上皮细胞A498对纯化的LPS无反应,然而,它们通过甘露糖敏感的附着介导途径对活细菌作出反应。为了鉴定膀胱上皮细胞识别的LPS成分,测试了一种细菌脂多糖A突变体和不同化学类型的LPS。完全诱导白细胞介素8需要六酰化脂多糖A,并且在存在O抗原的情况下降低50%至70%。综上所述,我们提出多种独立的途径,这些途径在器官和细胞中特异性表达,介导细菌识别并决定对感染的先天反应结果。