From the Manchester Collaborative Centre for Inflammation Research.
the Wellcome Trust Centre for Cell-Matrix Research, and.
J Biol Chem. 2018 Jun 1;293(22):8543-8553. doi: 10.1074/jbc.M117.789305. Epub 2018 Mar 26.
Cross-talk between different components of the intestinal barrier and the immune system may be important in maintaining gut homeostasis. A crucial part of the gut barrier is the mucus layer, a cross-linked gel on top of the intestinal epithelium that consists predominantly of the mucin glycoprotein MUC2. However, whether the mucin layer actively regulates intestinal immune cell responses is not clear. Because recent evidence suggests that intestinal dendritic cells (DCs) may be regulated by the mucus layer, we purified intestinal mucin, incubated it with human DCs, and determined the functional effects. Here we show that expression of the chemokine IL-8 and co-stimulatory DC markers CD86 and CD83 are significantly up-regulated on human DCs in the presence of intestinal mucins. Additionally, mucin-exposed DCs promoted neutrophil migration in an IL-8-dependent manner. The stimulatory effects of mucins on DCs were not due to mucin sample contaminants such as lipopolysaccharide, DNA, or contaminant proteins. Instead, mucin glycans are important for the pro-inflammatory effects on DCs. Thus, intestinal mucins are capable of inducing important pro-inflammatory functions in DCs, which could be important in driving inflammatory responses upon intestinal barrier damage.
肠道屏障和免疫系统的不同成分之间的串扰可能对于维持肠道内稳态很重要。肠道屏障的一个关键部分是黏液层,这是一种位于肠上皮细胞顶部的交联凝胶,主要由黏蛋白糖蛋白 MUC2 组成。然而,黏液层是否主动调节肠道免疫细胞的反应尚不清楚。因为最近的证据表明,肠道树突状细胞(DC)可能受到黏液层的调节,所以我们纯化了肠道黏蛋白,用其孵育人源 DC,并确定了其功能影响。在这里,我们表明,在存在肠道黏蛋白的情况下,人源 DC 中趋化因子 IL-8 和共刺激 DC 标志物 CD86 和 CD83 的表达显著上调。此外,黏蛋白暴露的 DC 以依赖于 IL-8 的方式促进中性粒细胞的迁移。黏蛋白对 DC 的刺激作用不是由于黏蛋白样品中的污染物(如脂多糖、DNA 或污染物蛋白)引起的。相反,黏蛋白聚糖对于 DC 的促炎作用很重要。因此,肠道黏蛋白能够诱导 DC 中重要的促炎功能,这可能对于肠道屏障损伤时引发炎症反应很重要。