Marin Maia, Holani Ravi, Shah Chaitanya B, Odeón Anselmo, Cobo Eduardo R
National Scientific and Technical Research Council (CONICET), Argentina.
Production Animal Health, Faculty of Veterinary Medicine, University of Calgary, Canada.
Mol Immunol. 2017 Nov;91:249-258. doi: 10.1016/j.molimm.2017.09.011. Epub 2017 Oct 5.
Cathelicidin are innate antimicrobial peptides with broad immunomodulatory functions; however, their role in regulating intestinal defenses is not well characterized. This study aimed to investigate the role of cathelicidin modulating expression of Toll-like receptors (TLRs) 4 and 9 in colonic epithelium in response to bacterial patterns. We demonstrated herein that intestinal epithelial cells, when primed by bacterial lipopolysaccharide (LPS), responded to cathelicidin by increased transcription and protein synthesis of TLR4. This cathelicidin-induced response required the interaction of LPS-TLR4 and activation of MAPK signalling pathways. However, cathelicidin blocked TLR9 responses induced by TLR9 ligand CpG oligodeoxynucleotide (CpG ODN) in these colonic epithelial cells. Modulations of TLRs triggered by cathelicidin in intestinal epithelium occurred mainly in the apical compartment of intestinal cells. Activation of TLR4 by ligands in combination with cathelicidin promoted CXCL8 chemokine secretion and epithelial antimicrobial defenses against Escherichia coli. We concluded that cathelicidin selectively modulated synthesis of TLR4 and 9 in intestinal epithelium, but only when cells were exposed to virulence factors, mostly from apical surfaces. Enhanced TLR4 expression promoted by cathelicidin in intestinal epithelium may be crucial for controlling enteric infectious diseases.
cathelicidin是具有广泛免疫调节功能的先天性抗菌肽;然而,它们在调节肠道防御中的作用尚未得到充分表征。本研究旨在探讨cathelicidin在结肠上皮细胞中调节Toll样受体(TLR)4和9表达以响应细菌模式的作用。我们在此证明,当肠道上皮细胞由细菌脂多糖(LPS)启动时,对cathelicidin的反应是TLR4的转录和蛋白质合成增加。这种cathelicidin诱导的反应需要LPS-TLR4的相互作用和MAPK信号通路的激活。然而,cathelicidin在这些结肠上皮细胞中阻断了由TLR9配体CpG寡脱氧核苷酸(CpG ODN)诱导的TLR9反应。cathelicidin在肠道上皮细胞中引发的TLR调节主要发生在肠道细胞的顶端隔室。配体与cathelicidin联合激活TLR4促进了CXCL8趋化因子的分泌以及上皮细胞对大肠杆菌的抗菌防御。我们得出结论,cathelicidin选择性地调节肠道上皮细胞中TLR4和9的合成,但仅当细胞暴露于主要来自顶端表面的毒力因子时才会如此。cathelicidin在肠道上皮细胞中促进的TLR4表达增强可能对控制肠道传染病至关重要。