Division of Gastroenterology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Division of Pediatric Gastroenterology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Sci Rep. 2019 Feb 4;9(1):1223. doi: 10.1038/s41598-018-38125-x.
Macrophages (Mϕs) are known to be major producers of the anti-inflammatory cytokine interleukin-10 (IL-10) in the intestine, thus playing an important role in maintaining gastrointestinal homeostasis. Mϕs that reside in the small intestine (SI) have been previously shown to be regulated by dietary antigens, while colonic Mϕs are regulated by the microbiota. However, the role which resident Mϕs play in SI homeostasis has not yet been fully elucidated. Here, we show that SI Mϕs regulate the integrity of the epithelial barrier via secretion of IL-10. We used an animal model of non-steroidal anti-inflammatory drug (NSAID)-induced SI epithelial injury to show that IL-10 is mainly produced by MHCII CD64 Ly6C Mϕs early in injury and that it is involved in the restoration of the epithelial barrier. We found that a lack of IL-10, particularly its secretion by Mϕs, compromised the recovery of SI epithelial barrier. IL-10 production by MHCII CD64 Ly6C Mϕs in the SI is not regulated by the gut microbiota, hence depletion of the microbiota did not influence epithelial regeneration in the SI. Collectively, these results highlight the critical role IL-10-producing Mϕs play in recovery from intestinal epithelial injury induced by NSAID.
巨噬细胞(Mϕs)是肠道中抗炎细胞因子白细胞介素 10(IL-10)的主要产生细胞,因此在维持胃肠道稳态方面发挥着重要作用。先前已经表明,驻留在小肠(SI)中的 Mϕs 受到膳食抗原的调节,而结肠 Mϕs 则受到微生物群的调节。然而,驻留 Mϕs 在 SI 稳态中的作用尚未完全阐明。在这里,我们显示 SI Mϕs 通过分泌 IL-10 来调节上皮屏障的完整性。我们使用非甾体抗炎药(NSAID)诱导的 SI 上皮损伤动物模型表明,IL-10 主要由 MHCII CD64 Ly6C Mϕs 在损伤早期产生,并且它参与上皮屏障的恢复。我们发现,缺乏 IL-10,特别是 Mϕs 的分泌,会损害 SI 上皮屏障的恢复。SI 中 MHCII CD64 Ly6C Mϕs 的 IL-10 产生不受肠道微生物群的调节,因此微生物群的耗竭不会影响 SI 上皮的再生。总的来说,这些结果强调了产生 IL-10 的 Mϕs 在 NSAID 诱导的肠道上皮损伤恢复中的关键作用。