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嗜酸乳杆菌通过转录机制刺激 SLC26A3 的表达。

Lactobacillus acidophilus stimulates the expression of SLC26A3 via a transcriptional mechanism.

机构信息

Department of Medicine, University of Illinois at Chicago and Jesse Brown Veterans Affairs Medical Center, 60612, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2010 Mar;298(3):G395-401. doi: 10.1152/ajpgi.00465.2009. Epub 2009 Dec 31.

Abstract

Clinical efficacy of probiotics in treating various forms of diarrhea has been clearly established. However, mechanisms underlying antidiarrheal effects of probiotics are not completely defined. Diarrhea is caused either by decreased absorption or increased secretion of electrolytes and solutes in the intestine. In this regard, the electroneutral absorption of two major electrolytes, Na(+) and Cl(-), occurs mainly through the coupled operation of Na(+)/H(+) exchangers and Cl(-)/OH(-) exchangers. Previous studies from our laboratory have shown that Lactobacillus acidophilus (LA) acutely stimulated Cl(-)/OH(-) exchange activity via an increase in the surface levels of the apical anion exchanger SLC26A3 (DRA). However, whether probiotics influence SLC26A3 expression and promoter activity has not been examined. The present studies were, therefore, undertaken to investigate the long-term effects of LA on SLC26A3 expression and promoter activity. Treatment of Caco-2 cells with LA for 6-24 h resulted in a significant increase in Cl(-)/OH(-) exchange activity. DRA mRNA levels were also significantly elevated in response to LA treatment starting as early as 8 h. Additionally, the promoter activity of DRA was increased by more than twofold following 8 h LA treatment of Caco-2 cells. Similar to the in vitro studies, in vivo studies using mice gavaged with LA also showed significantly increased DRA mRNA ( approximately 4-fold) and protein expression in the colonic regions as assessed by Western blot analysis and immunofluorescence. In conclusion, increase in DRA promoter activity and expression may contribute to the upregulation of intestinal electrolyte absorption and might underlie the potential antidiarrheal effects of LA.

摘要

益生菌治疗各种类型腹泻的临床疗效已得到明确证实。然而,益生菌止泻作用的机制尚未完全明确。腹泻要么是由于肠道内电解质和溶质的吸收减少,要么是分泌增加所致。在这方面,两种主要电解质(Na(+)和 Cl(-))的电中性吸收主要通过 Na(+)/H(+)交换器和 Cl(-)/OH(-)交换器的偶联操作来实现。我们实验室之前的研究表明,嗜酸乳杆菌(LA)通过增加顶端阴离子交换器 SLC26A3(DRA)的表面水平,急性刺激 Cl(-)/OH(-)交换活性。然而,益生菌是否影响 SLC26A3 的表达和启动子活性尚未得到检验。因此,本研究旨在探讨 LA 对 SLC26A3 表达和启动子活性的长期影响。用 LA 处理 Caco-2 细胞 6-24 h 可显著增加 Cl(-)/OH(-)交换活性。DRA mRNA 水平也随着 LA 处理的开始而在 8 h 时显著升高。此外,LA 处理 Caco-2 细胞 8 h 后,DRA 的启动子活性增加了两倍多。与体外研究相似,用 LA 灌胃的体内研究也显示,用 Western blot 分析和免疫荧光法评估,在结肠区域 DRA mRNA(约 4 倍)和蛋白表达显著增加。总之,DRA 启动子活性和表达的增加可能有助于肠道电解质吸收的上调,这可能是 LA 潜在的止泻作用的基础。

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