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短链脂肪酸通过对肠道肌成纤维细胞产生前列腺素E(1)和E(2)的不同影响来刺激上皮粘蛋白2的表达。

Short chain fatty acids stimulate epithelial mucin 2 expression through differential effects on prostaglandin E(1) and E(2) production by intestinal myofibroblasts.

作者信息

Willemsen L E M, Koetsier M A, van Deventer S J H, van Tol E A F

机构信息

Numico Research BV, Wageningen, the Netherlands.

出版信息

Gut. 2003 Oct;52(10):1442-7. doi: 10.1136/gut.52.10.1442.

Abstract

BACKGROUND

The mucus layer protects the gastrointestinal mucosa from mechanical, chemical, and microbial challenge. Mucin 2 (MUC-2) is the most prominent mucin secreted by intestinal epithelial cells. There is accumulating evidence that subepithelial myofibroblasts regulate intestinal epithelial cell function and are an important source of prostaglandins (PG). PG enhance mucin secretion and are key players in mucoprotection. The role of bacterial fermentation products in these processes deserves further attention.

AIMS

We therefore determined whether the effect of short chain fatty acids (SCFA) on MUC-2 expression involves intermediate PG production.

METHODS

Both mono- and cocultures of epithelial cells and myofibroblasts were used to study the effects of SCFA on MUC-2 expression and PG synthesis. Cell culture supernatants were used to determine the role of myofibroblast derived prostaglandins in increasing MUC-2 expression in epithelial cells.

RESULTS

Prostaglandin E(1) (PGE(1)) was found to be far more potent than PGE(2) in stimulating MUC-2 expression. SCFA supported a mucoprotective PG profile, reflected by an increased PGE(1)/PGE(2) ratio in myofibroblast supernatants and increased MUC-2 expression in mono- and cocultures. Incubation with indomethacin revealed the latter to be mediated by PG.

CONCLUSIONS

SCFA can differentially regulate PG production, thus stimulating MUC-2 expression in intestinal epithelial cells. This mechanism involving functional interaction between myofibroblasts and epithelial cells may play an important role in the mucoprotective effect of bacterial fermentation products.

摘要

背景

黏液层可保护胃肠道黏膜免受机械、化学和微生物的侵害。黏蛋白2(MUC - 2)是肠道上皮细胞分泌的最主要的黏蛋白。越来越多的证据表明,上皮下肌成纤维细胞调节肠道上皮细胞功能,并且是前列腺素(PG)的重要来源。PG可增强黏蛋白分泌,是黏膜保护的关键因素。细菌发酵产物在这些过程中的作用值得进一步关注。

目的

因此,我们确定短链脂肪酸(SCFA)对MUC - 2表达的影响是否涉及中间产物PG的产生。

方法

采用上皮细胞与肌成纤维细胞的单培养和共培养来研究SCFA对MUC - 2表达和PG合成的影响。细胞培养上清液用于确定肌成纤维细胞衍生的前列腺素在上皮细胞中增加MUC - 2表达的作用。

结果

发现前列腺素E(1)(PGE(1))在刺激MUC - 2表达方面比PGE(2)有效得多。SCFA支持黏膜保护的PG谱,表现为肌成纤维细胞上清液中PGE(1)/PGE(2)比值增加,以及单培养和共培养中MUC - 2表达增加。用吲哚美辛孵育表明后者由PG介导。

结论

SCFA可差异调节PG的产生,从而刺激肠道上皮细胞中MUC - 2的表达。这种涉及肌成纤维细胞与上皮细胞之间功能相互作用的机制可能在细菌发酵产物的黏膜保护作用中起重要作用。

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