CNRS, Centrale Marseille, iSm2, UMR 7313, Aix Marseille University, 13397, Marseille, France.
Toxalim (Research Centre in Food Toxicology), INRA, ENVT, INP-Purpan, UPS, Université de Toulouse, 31027, Toulouse, France.
Arch Toxicol. 2019 Apr;93(4):1039-1049. doi: 10.1007/s00204-019-02425-6. Epub 2019 Mar 11.
Trefoil factors (TFFs) are bioactive peptides expressed by several epithelia, including the intestine, where they regulate key functions such as tissue regeneration, barrier function and inflammation. Although food-associated mycotoxins, including deoxynivalenol (DON), are known to impact many intestinal functions, modulation of TFFs during mycotoxicosis has never been investigated. Here, we analyzed the effect of DON on TFFs expression using both human goblet cells (HT29-16E cells) and porcine intestinal explants. Results showed that very low doses of DON (nanomolar range) inhibit the secretion of TFFs by human goblet cells (IC of 361, 387 and 243 nM for TFF1, 2 and 3, respectively) and prevent wound healing. RT-qPCR analysis demonstrated that the inhibitory effect of DON is related to a suppression of TFFs mRNA expression. Experiments conducted on porcine intestinal explants confirmed the results obtained on cells. Finally, the use of specific inhibitors of signal pathways demonstrated that DON-mediated suppression of TFFs expression mainly involved Protein Kinase R and the MAP kinases (MAPK) p38 and ERK1/2. Taken together, our results show for the first time that at very low doses, DON suppresses the expression and production of intestinal TFFs and alters wound healing. Given the critical role of TFFs in tissue repair, our results suggest that DON-mediated suppression of TFFs contributes to the alterations of intestinal integrity the caused by this toxin.
三叶因子 (TFFs) 是几种上皮细胞表达的生物活性肽,包括肠道,它们调节组织再生、屏障功能和炎症等关键功能。尽管与食物相关的霉菌毒素,如脱氧雪腐镰刀菌烯醇 (DON),已知会影响许多肠道功能,但霉菌毒素中毒期间 TFFs 的调节从未被研究过。在这里,我们使用人杯状细胞 (HT29-16E 细胞) 和猪肠外植体分析了 DON 对 TFFs 表达的影响。结果表明,极低剂量的 DON(纳摩尔范围)抑制人杯状细胞 TFFs 的分泌(TFF1、2 和 3 的 IC 分别为 361、387 和 243 nM)并阻止伤口愈合。RT-qPCR 分析表明,DON 的抑制作用与 TFFs mRNA 表达的抑制有关。在猪肠外植体上进行的实验证实了细胞上获得的结果。最后,使用信号通路的特异性抑制剂表明,DON 介导的 TFFs 表达抑制主要涉及蛋白激酶 R 和丝裂原活化蛋白激酶 (MAPK) p38 和 ERK1/2。总之,我们的结果首次表明,在非常低的剂量下,DON 抑制肠道 TFFs 的表达和产生并改变伤口愈合。鉴于 TFFs 在组织修复中的关键作用,我们的结果表明,DON 介导的 TFFs 抑制作用导致该毒素引起的肠道完整性改变。