Variability in human hepatic MRP4 expression: influence of cholestasis and genotype

被引:68
作者
Gradhand, U. [1 ]
Lang, T. [2 ]
Schaeffeler, E. [3 ,4 ]
Glaeser, H. [1 ]
Tegude, H. [3 ,4 ]
Klein, K. [3 ,4 ]
Fritz, P. [5 ]
Jedlitschky, G. [6 ]
Kroemer, H. K.
Bachmakov, I. [1 ]
Anwald, B. [7 ]
Kerb, R. [7 ]
Zanger, U. M. [3 ,4 ]
Eichelbaum, M. [3 ,4 ]
Schwab, M. [3 ,4 ,8 ]
Fromm, M. F. [1 ]
机构
[1] Univ Erlangen Nurnberg, Inst Clin & Expt Pharmacol & Toxicol, D-91054 Erlangen, Germany
[2] Johannes Gutenberg Univ Mainz, Inst Pharmacol, Mainz, Germany
[3] Dr Margarete Fischer Bosch Inst Clin Pharmacol, D-7000 Stuttgart, Germany
[4] Univ Tubingen, Tubingen, Germany
[5] Robert Bosch Krankenhaus, Dept Pathol, Tubingen, Germany
[6] Ernst Moritz Arndt Univ Greifswald, Dept Pharmacol, Greifswald, Germany
[7] Pharmacogenet Lab, Bernried, Germany
[8] Univ Hosp Tuebingen, Dept Clin Pharmacol, Tubingen, Germany
关键词
MRP4; ABCC4; single nucleotide polymorphism; multidrug resistance; cholestasis; expression;
D O I
10.1038/sj.tpj.6500451
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The multidrug resistance protein 4 (MRP4) is an efflux transporter involved in the transport of endogenous substrates and xenobiotics. We measured MRP4 mRNA and protein expression in human livers and found a 38- and 45-fold variability, respectively. We sequenced 2 kb of the 5'-flanking region, all exons and intron/exon boundaries of the MRP4 gene in 95 patients and identified 74 genetic variants including 10 non-synonymous variations, seven of them being located in highly conserved regions. None of the detected polymorphisms was significantly associated with changes in the MRP4 mRNA or protein expression. Immunofluorescence microscopy indicated that none of the non-synonymous variations affected the cellular localization of MRP4. However, in cholestatic patients the MRP4 mRNA and protein expression both were significantly upregulated compared to non-cholestatic livers (protein: 299 +/- 138 vs 100 +/- 60a.u., P<0.001). Taken together, human hepatic MRP4 expression is highly variable. Genetic variations were not sufficient to explain this variability. In contrast, cholestasis is one major determinant of human hepatic MRP4 expression.
引用
收藏
页码:42 / 52
页数:11
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