Bryan Phillips-Farfán, Karla Carvajal, Edgar Alejandro Medina-Torres, Sara Elva Espinosa-Padilla, Gemma Fabrias, Luz Camacho
Laboratorio de Nutrición Experimental, Instituto Nacional de Pediatría, 04530 Ciudad de México, Mexico.
Unidad de Investigación en Inmunodeficiencias, Instituto Nacional de Pediatría, 04530 Ciudad de México, Mexico.
Mediators Inflamm. 2016;2016:9890141. doi: 10.1155/2016/9890141. Epub 2016 Aug 30.
Inflammatory bowel disease (IBD) describes different illnesses characterized by chronic inflammation of the gastrointestinal tract. Although the pathogenic mechanisms leading to IBD are poorly understood, immune system disturbances likely underlie its development. Sphingolipids (SLs) have been identified as important players and promising therapeutic targets to control inflammation in IBD. Interestingly, it seems that microorganisms of the normal gut microbiota and probiotics are involved in sphingolipid function. However, there is a great need to investigate the role of SLs as intermediates in the crosstalk between intestinal immunity and microorganisms. This review focuses on recent investigations that describe some mechanisms involved in the regulation of cytokine profiles by SLs. We also describe the importance of gut microbiota in providing signaling molecules that favor the communication between resident bacteria and intestinal cells. This, in turn, modulates the immune response in the bowel and likely in other peripheral organs. The potential of SLs and gut microbiota as targets or therapeutic agents for IBD is also discussed.
炎症性肠病(IBD)指的是一类以胃肠道慢性炎症为特征的不同疾病。尽管导致IBD的致病机制尚不清楚,但免疫系统紊乱可能是其发病的基础。鞘脂(SLs)已被确定为IBD中控制炎症的重要参与者和有前景的治疗靶点。有趣的是,正常肠道微生物群的微生物和益生菌似乎参与了鞘脂的功能。然而,迫切需要研究鞘脂作为肠道免疫与微生物之间相互作用的中间体的作用。本综述重点关注了最近的研究,这些研究描述了鞘脂调节细胞因子谱的一些机制。我们还描述了肠道微生物群在提供有利于常驻细菌与肠道细胞之间通讯的信号分子方面的重要性。这反过来又调节了肠道以及可能其他外周器官中的免疫反应。还讨论了鞘脂和肠道微生物群作为IBD靶点或治疗剂的潜力。