Extracellular glucose concentration alters functional activity of the intestinal oligopeptide transporter (PepT-1) in Caco-2 cells

被引:16
作者
D'Souza, VM
Buckley, DJ
Buckley, AR
Pauletti, GM
机构
[1] Univ Cincinnati, Med Ctr, Coll Pharm, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Med Ctr, Dept Mol & Cellular Physiol, Cincinnati, OH 45267 USA
关键词
Caco-2; cell; H plus /oligopeptide cotransporter; glucose; transport kinetics; oxidation;
D O I
10.1002/jps.10325
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The objective of this study was to determine the effect of different cell culture media glucose concentrations on the functional activity of PepT-1 in Caco-2 cells. Uptake kinetics of Gly-Sar into Caco-2 cells that were maintained in iso-osmotic media containing 25 or 5.5 mM glucose were determined in the presence and absence of amino acid-selective chemical modifiers and dithiothreitol. Inhibition of Gly-Sar uptake into Caco-2 cells was measured in the presence of dipeptides and xenobiotics exhibiting various binding affinities for the PepT-1. The effect of extracellular glucose on PepT-1 gene expression was assessed using comparative RT-PCR. Long-term exposure of Caeo-2 cells to 25 mM glucose reduced maximum transport capacity for Gly-Sar uptake without altering PepT-1 gene expression. In contrast, binding affinity of Gly-Sar and other dipeptides or xenobiotics was not significantly changed. Chemical modification of Lys and Tyr residues decreased V-max, while Cys modification increased the maximum transport capacity of the carrier. Preincubation of Caco-2 cells with dithiothreitol restored PepT-1 activity in cells maintained at 25 mM glucose. In conclusion, cell culture media containing 25 mM glucose decreases maximum transport capacity of PepT-1 in Caco-2 cells without affecting substrate recognition, at least in part, mediated via an oxidative pathway. (C) 2003 Wiley-Liss, lnc. and the American Pharmaceutical Association J Pharm Sci 92:594-603, 2003.
引用
收藏
页码:594 / 603
页数:10
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