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白三烯D4抑制肠上皮细胞中钠-丙氨酸共转运的机制。

Mechanism of leukotriene D4 inhibition of Na-alanine cotransport in intestinal epithelial cells.

作者信息

Talukder Jamilur R, Kekuda Ramesh, Saha Prosenjit, Sundaram Uma

机构信息

Section of Digestive Diseases, Department of Medicine, West Virginia University, Morgantown, WV 26506, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2008 Jul;295(1):G1-G6. doi: 10.1152/ajpgi.00498.2007. Epub 2008 Apr 24.

Abstract

In a rabbit model of chronic intestinal inflammation, we previously demonstrated inhibition of neutral Na-amino acid cotransport. The mechanism of the inhibition was secondary to a decrease in the affinity for amino acid rather than the number of cotransporters. Since leukotriene (LT)D4 is known to be elevated in enterocytes during chronic intestinal inflammation, we used rat intestinal epithelial cell (IEC-18) monolayers to determine the mechanism of regulation of Na-alanine cotransport (alanine, serine, cysteine transporter 1: ASCT1) by LTD4. Na-alanine cotransport was inhibited by LTD4 in IEC-18 cells. The mechanism of inhibition of ASCT1 (solute carrier, SLC1A4) by LTD4 is secondary to a decrease in the affinity of the cotransporter for alanine without a significant change in cotransporter numbers and is not secondary to an alteration in the Na+ extruding capacity of the cells. Real-time quantitative PCR and Western blot analysis results indicate that ASCT1 message and protein levels are also unchanged in LTD4-treated IEC-18 cells. These results indicate that LTD4 inhibits Na-dependent neutral amino acid cotransport in IEC. The mechanism of inhibition is secondary to a decrease in the affinity for alanine, which is identical to that seen in villus cells from the chronically inflamed rabbit small intestine, where LTD4 levels are significantly increased.

摘要

在慢性肠道炎症的兔模型中,我们之前证明了中性钠-氨基酸共转运受到抑制。这种抑制机制是由于对氨基酸的亲和力降低,而非共转运体数量减少。由于已知在慢性肠道炎症期间肠细胞中的白三烯(LT)D4水平会升高,我们使用大鼠肠上皮细胞(IEC-18)单层来确定LTD4对钠-丙氨酸共转运(丙氨酸、丝氨酸、半胱氨酸转运体1:ASCT1)的调节机制。在IEC-18细胞中,LTD4抑制了钠-丙氨酸共转运。LTD4对ASCT1(溶质载体,SLC1A4)的抑制机制是由于共转运体对丙氨酸的亲和力降低,而共转运体数量没有显著变化,且不是由于细胞的钠排出能力改变所致。实时定量PCR和蛋白质印迹分析结果表明,在经LTD4处理的IEC-18细胞中,ASCT1的信使核糖核酸和蛋白质水平也未改变。这些结果表明,LTD4抑制IEC中钠依赖性中性氨基酸共转运。抑制机制是由于对丙氨酸的亲和力降低,这与在慢性炎症兔小肠绒毛细胞中观察到的情况相同,在那里LTD4水平显著升高。

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Mechanism of leukotriene D4 inhibition of Na-alanine cotransport in intestinal epithelial cells.白三烯D4抑制肠上皮细胞中钠-丙氨酸共转运的机制。
Am J Physiol Gastrointest Liver Physiol. 2008 Jul;295(1):G1-G6. doi: 10.1152/ajpgi.00498.2007. Epub 2008 Apr 24.

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