Toll‐like receptor (TLR) 2 agonists ameliorate indomethacin‐induced murine ileitis by suppressing the TLR4 signaling

• DOI: 10.1111/jgh.12980
• Publication Date: 2015-04-13T10:29:38Z
• Authors: Kazuyuki Narimatsu; Masaaki Higashiyama; Chie Kurihara; Takeshi Takajo; Koji Maruta; Yuichi Yasutake; Hirokazu Sato; Yoshikiyo Okada; Chikako Watanabe; Shunsuke Komoto; Kengo Tomita; Shigeaki Nagao; Soichiro Miura; Ryota Hokari
• Keywords: Lipopolysaccharides; 0301 basic medicine; Dose-Response Relationship, Drug; Anti-Inflammatory Agents, Non-Steroidal; Indomethacin; Gene Expression; Ileitis; Toll-Like Receptor 2; 3. Good health; Teichoic Acids; Disease Models, Animal; Mice; 03 medical and health sciences; RAW 264.7 Cells; Cell Migration Assays, Leukocyte; Cell Movement; Leukocytes; Animals; Cytokines; RNA, Messenger; Inflammation Mediators; Injections, Intraperitoneal; Signal Transduction

AbstractBackground and AimFew drugs have been found satisfactory in the treatment of nonsteroidal anti‐inflammatory drugs (NSAIDs)‐induced enteropathy. Toll‐like receptor (TLR) 4 and aberrant leukocyte migration to the intestinal mucosa are reported to be involved in the pathology of intestinal enteropathy and TLR2 agonists have been found to evoke hyposensitivity to TLR4 stimulation in vitro. In this study, we investigated whether and how lipoarabinomannan (LAM) or lipoteichoic acid (LTA), TLR2 agonists, attenuated indomethacin (IND)‐induced intestinal damage.MethodsLAM (0.5 mg/kg) or LTA (15 mg/kg) was administered intraperitoneally to mice before IND (10 mg/kg) administration. Disease activity was evaluated macroscopically and histologically. In the migration analysis, fluorescence‐labeled leukocyte movement in the intestinal microvessels was observed by intravital microscopy. Expression of P‐selectin, MAdCAM‐1, TLR2, TLR4, and F4/80 was observed immunohistochemically. In the in vitro analysis, RAW264.7 macrophage cells were preincubated with LAM and stimulated with lipopolysaccharide (LPS), and the mRNA expression levels of TLR4, tumor necrosis factor‐α, and interleukin‐12p40 were measured.ResultsPretreatment with LAM or LTA significantly decreased IND‐induced injury as well as decreased leukocyte infiltration. Pretreatment with LAM decreased IND‐induced TLR4 expression on F4/80+ macrophages, the level of P‐selectin expression, and leukocyte migration in the small intestinal vessels. In the in vitro study, a single administration of LAM decreased TLR4 mRNA expression and inhibited the increase in mRNA expression of inflammatory cytokines by LPS in a dose‐dependent manner.ConclusionTLR2 agonists attenuated IND‐induced small intestinal lesions and leukocyte infiltration probably by suppressing the TLR4 signaling pathway in tissue macrophages.