Koitabashi A, Shimada T, Fujii Y, Hashimoto T, Hosaka K, Tabei K, Namatame T, Yoneda M, Hiraishi H, Terano A
Department of Gastroenterology and Institute for Medical Science, Dokkyo University School of Medicine, Mibu, Tochigi, Japan.
Aliment Pharmacol Ther. 2004 Jul;20 Suppl 1:171-6. doi: 10.1111/j.1365-2036.2004.01991.x.
Trefoil factor family peptides are expressed in gastrointestinal epithelial cells and play a critical role in maintaining mucosal integrity. Although non-steroidal anti-inflammatory drugs (NSAIDs) are important causative agents of gastric mucosal lesions, few data are available about the effect of NSAIDs on trefoil family peptides in gastric mucosa.
To examine whether indometacin, a widely used NSAID, affects trefoil factor family expression in gastric epithelial cells.
MKN45, a cell line derived from human gastric cancer, was used. TFF1, TFF2, and TFF3 mRNA expression was assessed by real-time quantitative reverse transcription-polymerase chain reaction (RT-PCR). TFF2 gene transcription was also examined by luciferase reporter gene assay.
Relative expression level of TFF1, TFF2, TFF3 mRNA was 616: 12: 1 in unstimulated MKN45 cells. Although indometacin (1-250 micro mol/L) had no significant effect on the expression of TFF1 and TFF3 mRNA, it up-regulated TFF2 mRNA expression in a dose- and time-dependent manner. Luciferase reporter gene assay confirmed the up-regulation of TFF2 gene transcription by indometacin. Indometacin-induced up-regulation of TFF2 expression was not antagonized by externally applied prostaglandin E2.
These results suggest that indometacin up-regulates gastric epithelial cell TFF2 expression through a COX-independent mechanism. Since TFF peptides play an important role in gastric mucosal protection, indometacin-induced TFF2 may reduce the degree of gastric mucosal damage induced by indometacin.
三叶因子家族肽在胃肠道上皮细胞中表达,对维持黏膜完整性起关键作用。尽管非甾体抗炎药(NSAIDs)是胃黏膜损伤的重要致病因素,但关于NSAIDs对胃黏膜中三叶因子家族肽的影响的数据却很少。
研究广泛使用的NSAIDs吲哚美辛是否影响胃上皮细胞中三叶因子家族的表达。
使用源自人胃癌的MKN45细胞系。通过实时定量逆转录-聚合酶链反应(RT-PCR)评估TFF1、TFF2和TFF3 mRNA的表达。还通过荧光素酶报告基因检测法检测TFF2基因转录。
在未刺激的MKN45细胞中,TFF1、TFF2、TFF3 mRNA的相对表达水平为616:12:1。尽管吲哚美辛(1-250微摩尔/升)对TFF1和TFF3 mRNA的表达没有显著影响,但它以剂量和时间依赖性方式上调TFF2 mRNA的表达。荧光素酶报告基因检测法证实吲哚美辛可上调TFF2基因转录。外源性应用前列腺素E2不能拮抗吲哚美辛诱导的TFF2表达上调。
这些结果表明,吲哚美辛通过一种不依赖环氧化酶(COX)的机制上调胃上皮细胞TFF2的表达。由于三叶因子肽在胃黏膜保护中起重要作用,吲哚美辛诱导的TFF2可能会减轻吲哚美辛诱导的胃黏膜损伤程度。