σ receptor ligand-induced up-regulation of the H+/peptide transporter PEPT1 in the human intestinal cell line Caco-2

被引:38
作者
Fujita, T [1 ]
Majikawa, Y
Umehisa, S
Okada, N
Yamamoto, A
Ganapathy, V
Leibach, FH
机构
[1] Kyoto Pharmaceut Univ, Dept Biopharmaceut Sci, Yamashina Ku, Kyoto 6078414, Japan
[2] Med Coll Georgia, Dept Biochem & Mol Biol, Augusta, GA 30912 USA
基金
日本学术振兴会;
关键词
D O I
10.1006/bbrc.1999.1026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We determined the effects of (+)pentazocine, a selective a, ligand, on the uptake of glycylsarcosine (Gly-Sar) in the human intestinal cell line Caco-2 which expresses the low affinity/high capacity peptide transporter PEPT1. Confluent Caco-2 cells were treated with various concentrations of (+)pentazocine for desired time (mostly 24 hr). The activity of PEPT1 was assessed by measuring the uptake of [C-14]Gly-Sar in the presence of a H+ gradient. (+)Pentazocine increased the uptake of [C-14]Gly-Sar mediated by PEPT1 in a concentration- and time-dependent manner. Kinetic analyses have indicated that (+)pentazocine increased the maximal velocity (V-max) for Gly-Sar uptake in Caco-2 cells without affecting the Michaelis Menten constant (K-t). In addition, semi-quantitative RT-PCR revealed that treatment of (+)pentazocine increased PEPT1 mRNA in Caco-2 cells in a concentration-dependent manner. These data suggest that a, receptor ligand (+)pentazocine up-regulates PEPT1 in Caco-2 cells at the level of increased mRNA, causing an increase in the density of the transporter protein in the cell membrane. (C) 1999 Academic Press.
引用
收藏
页码:242 / 246
页数:5
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