Manoharan Palanikumar, Gayam Swapna, Arthur Subha, Palaniappan Balasubramanian, Singh Soudamani, Dick Gregory M, Sundaram Uma
Department of Biochemistry and Microbiology, University of Cincinnati, Cincinnati, Ohio;
Section of Digestive Diseases, West Virginia University, Morgantown, West Virginia;
Am J Physiol Cell Physiol. 2015 Apr 15;308(8):C650-6. doi: 10.1152/ajpcell.00355.2014. Epub 2015 Feb 4.
Na-K-ATPase, an integral membrane protein in mammalian cells, is responsible for maintaining the favorable intracellular Na gradient necessary to promote Na-coupled solute cotransport processes [e.g., Na-glucose cotransport (SGLT1)]. Inhibition of brush border membrane (BBM) SGLT1 is, at least in part, due to the diminished Na-K-ATPase in villus cells from chronically inflamed rabbit intestine. The aim of the present study was to determine the effect of Na-K-ATPase inhibition on the two major BBM Na absorptive pathways, specifically Na-glucose cotransport and Na/H exchange (NHE), in intestinal epithelial (IEC-18) cells. Na-K-ATPase was inhibited using 1 mM ouabain or siRNA for Na-K-ATPase-α1 in IEC-18 cells. SGLT1 activity was determined as 3-O-methyl-D-[(3)H]glucose uptake. Na-K-ATPase activity was measured as the amount of inorganic phosphate released. Treatment with ouabain resulted in SGLT1 inhibition at 1 h but stimulation at 24 h. To further characterize this unexpected stimulation of SGLT1, siRNA silencing was utilized to inhibit Na-K-ATPase-α1. SGLT1 activity was significantly upregulated by Na-K-ATPase silencing, while NHE3 activity remained unaltered. Kinetics showed that the mechanism of stimulation of SGLT1 activity was secondary to an increase in affinity of the cotransporter for glucose without a change in the number of cotransporters. Molecular studies demonstrated that the mechanism of stimulation was not secondary to altered BBM SGLT1 protein levels. Chronic and direct silencing of basolateral Na-K-ATPase uniquely regulates BBM Na absorptive pathways in intestinal epithelial cells. Specifically, while BBM NHE3 is unaffected, SGLT1 is stimulated secondary to enhanced affinity of the cotransporter.
钠钾ATP酶是哺乳动物细胞中的一种整合膜蛋白,负责维持促进钠偶联溶质共转运过程(如钠葡萄糖共转运(SGLT1))所需的有利细胞内钠梯度。刷状缘膜(BBM)SGLT1的抑制至少部分是由于慢性炎症兔肠道绒毛细胞中钠钾ATP酶减少所致。本研究的目的是确定钠钾ATP酶抑制对肠道上皮(IEC - 18)细胞中两个主要的BBM钠吸收途径,即钠葡萄糖共转运和钠氢交换(NHE)的影响。在IEC - 18细胞中,使用1 mM哇巴因或针对钠钾ATP酶α1的小干扰RNA(siRNA)抑制钠钾ATP酶。SGLT1活性通过3 - O - 甲基 - D - [(3)H]葡萄糖摄取来测定。钠钾ATP酶活性以释放的无机磷酸量来测量。用哇巴因处理在1小时时导致SGLT1抑制,但在24小时时导致刺激。为了进一步表征这种对SGLT1的意外刺激,利用siRNA沉默来抑制钠钾ATP酶α1。钠钾ATP酶沉默显著上调了SGLT1活性,而NHE3活性保持不变。动力学表明,SGLT1活性刺激的机制是由于共转运体对葡萄糖的亲和力增加,而共转运体数量没有变化。分子研究表明,刺激机制并非继发于BBM SGLT1蛋白水平的改变。基底外侧钠钾ATP酶的慢性和直接沉默独特地调节肠道上皮细胞中的BBM钠吸收途径。具体而言,虽然BBM NHE3不受影响,但SGLT1因共转运体亲和力增强而受到刺激。