Damiano Simona, Sasso Anna, De Felice Bruna, Di Gregorio Ilaria, La Rosa Giuliana, Lupoli Gelsi A, Belfiore Anna, Mondola Paolo, Santillo Mariarosaria
Dipartimento di Medicina Clinica e Chirurgia, Università di Napoli "Federico II", Naples, Italy.
Dipartimento di Scienze e Tecnologie Ambientali Biologiche e Farmaceutiche, Università della Campania Luigi Vanvitelli, Caserta, Italy.
Front Physiol. 2018 Apr 6;9:357. doi: 10.3389/fphys.2018.00357. eCollection 2018.
The main dietary flavonoid quercetin, is known to preserve the integrity of gastrointestinal barrier and to have anti-inflammatory, anti-cancer, anti-fibrotic, and other beneficial properties. Many of the biological effects of quercetin appear to be associated to the modulation of cell signaling pathways, rather than to its antioxidant activity. In spite of the large number of data available on the molecular and cellular mechanisms by which quercetin exerts its biological effects, including protection of intestinal barrier function, there is a lack of data about the role of this substance on the expression and/or the secretion of mucins released by intestinal goblet cells. Here we investigated the effects of quercetin on the secretion and the gene expression of the main intestinal gel-forming mucins, MUC2 and MUC5AC, and the signaling mechanisms underlined, in human intestinal goblet cell-like LS174T. We found that quercetin increases intracellular Ca levels and induces MUC2 and MUC5AC secretion in a Ca-dependent manner. Quercetin also induces mRNA levels of both secretory mucins. Quercetin stimulation of LS174T cells increases phosphorylation levels of extracellular signal regulated kinase (ERK)1-2 and protein kinase C (PKC) α and the induction of MUC2 and MUC5AC secretion and mRNA relies on phospholipase C (PLC), PKC, and ERK1-2 signaling pathways since the PLC inhibitor U73122, the PKC inhibitor bisindolylmaleimide (BIM) and the ERK1-2 pathway inhibitor PD98059, all revert the stimulatory effects of quercetin. We also demonstrated that the induction of mucin gene expression by quercetin is not limited to goblet cells. Indeed, quercetin induces mRNA levels of MUC2 and MUC5AC via PKCα/ERK1-2 pathway also in the human intestinal epithelial Caco-2 cells. These data highlight a novel mechanism thereby quercetin, regulating the secretory function of intestinal goblet cells and mucin levels in enterocytes may exert its protective effects on intestinal mucosal barrier.
主要的膳食类黄酮槲皮素,已知可维持胃肠道屏障的完整性,并具有抗炎、抗癌、抗纤维化等有益特性。槲皮素的许多生物学效应似乎与细胞信号通路的调节有关,而不是与其抗氧化活性有关。尽管有大量关于槲皮素发挥其生物学效应的分子和细胞机制的数据,包括对肠道屏障功能的保护,但关于该物质对肠道杯状细胞释放的粘蛋白表达和/或分泌的作用的数据却很缺乏。在此,我们研究了槲皮素对人肠道杯状细胞样LS174T中主要的肠道凝胶形成粘蛋白MUC2和MUC5AC的分泌及基因表达的影响,以及相关的信号传导机制。我们发现槲皮素可增加细胞内钙离子水平,并以钙离子依赖的方式诱导MUC2和MUC5AC的分泌。槲皮素还可诱导两种分泌性粘蛋白的mRNA水平。槲皮素对LS174T细胞的刺激可增加细胞外信号调节激酶(ERK)1-2和蛋白激酶C(PKC)α的磷酸化水平,而MUC2和MUC5AC分泌及mRNA的诱导依赖于磷脂酶C(PLC)、PKC和ERK1-2信号通路,因为PLC抑制剂U73122、PKC抑制剂双吲哚马来酰亚胺(BIM)和ERK1-2通路抑制剂PD98059均可逆转槲皮素的刺激作用。我们还证明,槲皮素对粘蛋白基因表达的诱导并不局限于杯状细胞。事实上,槲皮素在人肠道上皮Caco-2细胞中也通过PKCα/ERK1-2通路诱导MUC2和MUC5AC的mRNA水平。这些数据突出了一种新机制,即槲皮素通过调节肠道杯状细胞的分泌功能和肠上皮细胞中的粘蛋白水平,可能对肠道黏膜屏障发挥保护作用。