Department of Medicine, Division of Digestive Diseases, Emory University School of Medicine, Atlanta GA 30322, USA.
Am J Physiol Gastrointest Liver Physiol. 2011 Jan;300(1):G52-9. doi: 10.1152/ajpgi.00394.2010. Epub 2010 Oct 28.
MicroRNAs (miRNAs), which are noncoding RNAs that posttranscriptionally inhibit expression of target genes, have recently emerged as important regulators of many cellular functions such as cell differentiation. The epithelial di/tripeptide membrane transporter PepT1 is expressed in highly differentiated cells (the villous tip) but not in undifferentiated cells (the crypt) of the small intestine. Here, we investigated the regulation of PepT1 expression by miRNAs and its functional consequences. We observed a reverse correlation between the expression levels of PepT1 and mature miRNA-92b (miR-92b) during the differentiation of intestinal epithelial Caco2-BBE cells, suggesting a miR-92b-mediated regulation of PepT1 expression. We demonstrate that miR-92b suppressed PepT1 expression at both mRNA and protein levels, with subsequent reduced PepT1 transport activity, in Caco2-BBE cells by directly targeting the PepT1 3'-untranslated region. In addition, miR-92b suppresses bacterial peptide-induced proinflammatory responses in intestinal epithelial cells by inhibiting PepT1 expression. Altogether, our study provides for the first time evidence for the regulation of PepT1 expression at a posttranscriptional level by miRNAs in intestinal epithelial cells during pathophysiological states.
微小 RNA(miRNA)是一种非编码 RNA,可在后转录水平抑制靶基因的表达,最近已成为许多细胞功能(如细胞分化)的重要调节因子。上皮二肽/三肽膜转运蛋白 PepT1 表达于高度分化的细胞(绒毛顶端),而不表达于未分化的细胞(隐窝)。在这里,我们研究了 miRNA 对 PepT1 表达的调节及其功能后果。我们观察到在肠上皮细胞 Caco2-BBE 的分化过程中,PepT1 的表达水平与成熟 miRNA-92b(miR-92b)呈负相关,提示 PepT1 的表达受到 miR-92b 的调节。我们证明,miR-92b 通过直接靶向 PepT1 3'-UTR,在 Caco2-BBE 细胞中抑制 PepT1 的表达,从而抑制 PepT1 转运活性,从而抑制 PepT1 的表达,抑制 PepT1 的表达,抑制 PepT1 的表达,抑制 PepT1 的表达,抑制 PepT1 的表达,抑制 PepT1 的表达。总之,我们的研究首次提供了证据,证明在生理病理状态下,miRNA 可在肠上皮细胞中对 PepT1 表达进行转录后水平的调节。