Genetics is a major determinant of expression of the human hepatic uptake transporter OATP1B1, but not of OATP1B3 and OATP2B1
- Anne T Nies1Email author,
- Mikko Niemi2,
- Oliver Burk1,
- Stefan Winter1,
- Ulrich M Zanger1,
- Bruno Stieger3,
- Matthias Schwab†1, 4 and
- Elke Schaeffeler†1
© Nies et al.; licensee BioMed Central Ltd. 2013
Received: 7 September 2012
Accepted: 11 January 2013
Published: 11 January 2013
Organic anion transporting polypeptide (OATP) 1B1, OATP1B3, and OATP2B1 (encoded by SLCO1B1, SLCO1B3, SLCO2B1) mediate the hepatic uptake of endogenous compounds like bile acids and of drugs, for example, the lipid-lowering atorvastatin, thereby influencing hepatobiliary elimination. Here we systematically elucidated the contribution of SLCO variants on expression of the three hepatic OATPs under consideration of additional important covariates.
Expression was quantified by RT-PCR and immunoblotting in 143 Caucasian liver samples. A total of 109 rare and common variants in the SLCO1B3-SLCO1B1 genomic region and the SLCO2B1 gene were genotyped by MALDI-TOF mass spectrometry and genome-wide SNP microarray technology. SLCO1B1 haplotypes affecting hepatic OATP1B1 expression were associated with pharmacokinetic data of the OATP1B1 substrate atorvastatin (n = 82).
Expression of OATP1B1, OATP1B3, and OATP2B1 at the mRNA and protein levels showed marked interindividual variability. All three OATPs were expressed in a coordinated fashion. By a multivariate regression analysis adjusted for non-genetic and transcription covariates, increased OATP1B1 expression was associated with the coding SLCO1B1 variant c.388A > G (rs2306283) even after correction for multiple testing (P = 0.00034). This held true for haplotypes harboring c.388A > G but not the functional variant c.521T > C (rs4149056) associated with statin-related myopathy. c.388A > G also significantly affected atorvastatin pharmacokinetics. SLCO variants and non-genetic and regulatory covariates together accounted for 59% of variability of OATP1B1 expression.
Our results show that expression of OATP1B1, but not of OATP1B3 and OATP2B1, is significantly affected by genetic variants. The SLCO1B1 variant c.388A > G is the major determinant with additional consequences on atorvastatin plasma levels.
The organic anion transporting polypeptides 1B1 (OATP1B1, encoded by the SLCO1B1 gene), OATP1B3 (SLCO1B3), and OATP2B1 (SLCO2B1) are major uptake transporters on the sinusoidal membrane of human hepatocytes. They mediate the influx of endogenous compounds such as bile salts, bilirubin glucuronides, thyroid hormones and steroid hormone metabolites, and clinically frequently used drugs like statins, HIV protease inhibitors, and the anti-cancer agents irinotecan or methotrexate [1–5]. The importance of OATP transporters for hepatobiliary uptake is emphasized by the Rotor syndrome, which is a two-gene disorder caused by the complete combined deficiency of OATP1B1 and OATP1B3 .
Numerous clinical studies support the relevance of common but also rare SLCO1B1 missense variants altering either the pharmacokinetics or drug response of OATP1B1 substrates [4, 7, 8]. The common variant c.521T > C (rs4149056; Val174Ala) is highlighted by a genome-wide association study (GWAS) suggesting an increased risk for simvastatin-induced myopathy in variant carriers . Reduced hepatic uptake of the OATP1B1 substrates atorvastatin and rosuvastatin is supported by in vitro experiments using cell lines stably expressing the c.521T > C variant [2, 10]. Moreover, the in vivo disposition of endogenous and/or xenobiotic substances, including drugs, is also affected by SLCO1B3 and SLCO2B1 variants .
Irrespective of well-established data on functional consequences of SLCO variants, the contribution of SLCO variants to the interindividual variability of hepatic expression of OATP transporters is still unknown. Although cholestasis has been recognized as an additional determinant of OATP1B1 and OATP1B3 expression , a comprehensive analysis including SLCO variants as well as non-genetic and regulatory covariates is presently lacking. Similar to recent work related to the hepatic uptake transporters OCT1 and OCT3 , we therefore investigated the impact of > 100 SLCO variants as well as non-genetic and regulatory covariates on the interindividual variability of hepatic OATP1B1, OATP1B3, and OATP2B1 expression. The transcription factors hepatocyte nuclear factor (HNF)1α, farnesoid X receptor (FXR), liver X receptor (LXR)α, specificity protein 1 (Sp1), aryl hydrocarbon receptor (AhR), constitutive androstane receptor (CAR), and HNF3β were selected because literature data indicate they are involved in regulation of the three hepatic SLCO genes with potential consequences on variability of expression [14–21]. The novel finding that the SLCO1B1 missense variant Asn130Asp (rs2306283) alters hepatic protein expression most effectively is supported by pharmacokinetic data of atorvastatin in a study of healthy volunteers. SLCO variants and non-genetic and regulatory covariates accounted for 59% of variability of hepatic OATP1B1 expression.
Materials and methods
Human liver samples
Liver tissue and corresponding blood samples were collected from patients undergoing liver surgery at the Department of General, Visceral, and Transplantation Surgery (University Medical Center Charité, Berlin, Germany) as described previously [13, 22, 23]. Tissue samples had been examined by a pathologist; only histologically normal liver tissue was used for further studies. For each patient, detailed information was available regarding age, sex, smoking status, alcohol consumption, presurgery medication, indication for liver resection, and presurgery liver serum parameters. Samples from patients with hepatitis, cirrhosis, or chronic alcohol use were excluded. A total of 143 liver samples from which high quality RNA and complete documentation could be obtained were finally included (Table S1 in Additional file 1). The study was approved by the ethics committees of the Charité, Humboldt University (Berlin, Germany) and the University of Tübingen (Tübingen, Germany) in accordance with the principles of the Declaration of Helsinki. Written informed consent was obtained from each patient.
Atorvastatin pharmacokinetics in vivo
Atorvastatin pharmacokinetic variables were obtained from 82 healthy volunteers (Table S2 in Additional file 1) as previously described [24–26]. Briefly, volunteers ingested a single 20 mg dose of atorvastatin (Lipitor; Pfizer/Gödecke, Karlsruhe, Germany). No other drugs or grapefruit products were consumed prior to atorvastatin administration . The study was approved by the Ethics Committee of the Hospital District of Helsinki and Uusimaa, Finland. Written informed consent was obtained from the participants.
Selection of genetic variants and genotyping strategies
Genomic DNA was purified from EDTA blood samples with the QIAmp DNA Blood MiniKit (Qiagen, Hilden, Germany). All samples were genotyped for 109 genetic variants (Figure S1 and Table S3 in Additional file 1). We selected 58 genetic variants of the SLCO1B3-SLCO1B1 genomic region (chromosome 12) and the SLCO2B1 gene (chromosome 11) from the National Center for Biotechnology Information database (dbSNP build 129) based on functional criteria and/or frequency distribution. Genotyping was performed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) using the MassARRAY Compact system (Sequenom, San Diego, CA, USA) or by 5'-nuclease assays (ABI Prism 7900 Sequence Detection System, Applied Biosystems/Life Technologies, Carlsbad, CA, USA). Moreover, 51 additional variants of the SLCO1B3-SLCO1B1 genomic region and the SLCO2B1 gene were genotyped using the HumanHap300v1.1 chip data set (Illumina, San Diego, CA, USA) as described previously  (NCBI Gene Expression Omnibus series GSE39036, GSE32504). For MALDI-TOF MS and TaqMan analysis, about 10% of samples were re-genotyped as quality control resulting in 100% concordance. Missing calls in MALDI-TOF MS and TaqMan genotyping were re-typed, resulting in final call rates of 99%. Laboratory staff were blinded to the case status of liver samples. Details of primers and genotyping assays are available upon request.
RNA isolation and quantification
Quantification of OATPs in human liver samples
Generation of HEK cells stably expressing OATP2B1 and missense variants
Human embryonic kidney (HEK) cells were transfected with constructs encoding human SLCO2B1 or the missense variants c.601G > A (rs35199625; GenBank: NM_007256.4 as reference), c.935G > A (rs12422149), and c.1457C > T (rs2306168) (Additional file 1).
Cryosections of liver samples were immunostained for OATP1B1 and OATP2B1 using previously characterized antibodies [29, 30]. Images were taken with a confocal laser scanning microscope (Additional file 1).
Transport studies and prediction of functional effects
Transport of atorvastatin, rosuvastatin, and estrone sulfate by OATP2B1 and variants was measured using stably-transfected HEK cells (Additional file 1). Functional effects of OATP2B1 missense variants were calculated using four different algorithms (Additional file 1).
Hardy-Weinberg equilibrium calculations [31, 32] were used to compare observed and expected allele and genotype frequencies. Linkage disequilibrium analysis of the SLCO1B3-SLCO1B1 genomic region and the SLCO2B1 gene was performed with Haploview  using results from our study population of 143 Caucasians. Haplotype analysis was performed with R-package haplo.stats-1.4.4  (R-2.13.0).
Multivariate analysis of hepatic OATP expression in relation to 10 non-genetic factors in the total sample set of 143 human livers
Hepatic OATP expression
Impact of non-genetic factors on OATP expression
Multivariate linear regression analyses showed no association between OATP expression and sex, age, smoking habit, presurgery medication, bilirubin levels, or γ-glutamyl transferase levels (Table 1). Alcohol consumption was significantly associated with reduced SLCO1B1 and SLCO2B1 mRNA levels. Pathophysiologically increased C-reactive protein levels were associated with reduced SLCO1B1 mRNA levels. As expected from previous studies , OATP1B1 and OATP1B3 protein levels were significantly lower in cholestatic liver samples. When analyzing only the non-cholestatic samples, alcohol consumption was again significantly associated with reduced SLCO2B1 mRNA levels (Table S5 in Additional file 1).
SLCO genetic variants and frequencies
SLCO/OATP genotype-phenotype correlation analyses
In order to exclude confounding by cholestasis, all subsequent analyses were performed with the non-cholestatic liver samples (n = 117). Multivariate linear regression models were used to analyze associations between variants with frequencies ≥ 1% in the SLCO1B3-SLCO1B1 genomic region and the SLCO2B1 gene (Figure S1 in Additional file 1) and the expression of OATP1B1, OATP1B3, and OATP2B1. Models were corrected for eight non-genetic covariates (Table S6 in Additional file 1) and the regulatory factors HNF1, LXR, FXR, HNF3, Sp1, CAR, and AhR previously suggested by literature data as transcriptional regulators of at least one SLCO gene [14–21]. Interindividual variability of the expression of these transcription factors is given in Table S4B in Additional file 1.
Considering the additive genetic model, 38 variants in the SLCO1B3-SLCO1B1 genomic region correlated with OATP1B1 or OATP1B3 expression, and 3 variants in the SLCO2B1 gene with OATP2B1 expression (Table S6 in Additional file 1). After multiple testing correction, 16 variants in the SLCO1B3-SLCO1B1 genomic region were still significantly associated with OATP1B1 expression. Notably, for the OATP1B1 protein, variant c.388A > G (Asn130Asp, rs2306283) showed the lowest P-value (P = 0.00034) whereas the variant c.521T > C (Val174Ala, rs4149056), associated with statin-induced myopathy [9, 35, 36], did not show any association. Stratification of baseline characteristics by carriers of c.388A > G (dominant model) did not show any significance.
Additionally, we calculated haplotypes for the non-cholestatic liver samples using different strategies. Firstly, haplotypes were calculated for genetic variants of SLCO1B1, SLCO1B3, and SLCO2B1 detected in the liver samples (Table S3 in Additional file 1). Only variants with a frequency ≥ 1% were included. Significant associations with substantial effect sizes between haplotypes and expression were only found for OATP1B1 protein and SLCO2B1 mRNA expression, even after correction for multiple testing (Tables S7 to S9 in Additional file 1). Secondly, previously reported SLCO1B1 haplotypes containing only the variants c.388A > G, c.463C > A, c.521T > C and c.1929A > C were calculated (Figure 2c). The haplotypes *1b (P = 0.0037), *14 (P = 1.8 × 10-5), and *35 (P = 0.0004), including the c.388A > G but not the c.521T > C variant, were significantly associated with increased OATP1B1 protein expression, even after multiple testing correction. These haplotypes exhibited substantial effect sizes (*1b, 0.43; *14, 0.53; *35, 0.56) and clustered with samples of highest median OATP1B1 expression (Figure 2d). OATP1B1 protein levels also increased with the number of *1b, *14, and *35 alleles (Figure S3A in Additional file 1).
Thirdly, we calculated haplotypes covering all variants of the SLCO1B3-SLCO1B1 genomic region (Table S10 in Additional file 1). Two haplotypes, which included the SLCO1B1 variant c.388A > G, were significantly associated with increased OATP1B1 protein levels and showed substantial effect sizes for the correlation (H-cluster04, 0.62; H-cluster12, 0.59).
Contribution of genetic, non-genetic, and transcription factors to variable OATP expression
Interindividual variability of hepatic OATP1B1 protein expression was substantially explained by SLCO1B1 variants (50%) while non-genetic (8%) and transcription factors (7%) contributed only to a minor extent (Figure 2e). Notably, 59% of variability could be apportioned to the combination of all three categories (that is, genetic, non-genetic, transcription factors). Total variance of OATP1B3 protein expression was explained to 55% by these categories but only 24% of variance of OATP2B1 protein expression could be apportioned to the three categories.
In order to identify whether the effects of variant c.388A > G may be confounded by variant c.521T > C, we conducted multivariate models including both variants simultaneously. The variant c.388A > G was significantly associated with decreased AUC for atorvastatin (P = 0.00066, recessive model) whereas the variant c.521T > C resulted in an increased AUC (P = 2.6 × 10-10, additive model). Of note, these data held true when the interaction effect of c.388A > G and c.521T > C was included into the model (c.388A > G, P = 0.00535; c.521T > C, P = 3.0 × 10-7; interaction effect, P = 0.67).
Statin transport by OATP2B1 and its missense variants
The SLCO2B1 missense variants c.601G > A, c.935G > A and c.1457C > T were the only ones present in our liver cohort (Table S3 in Additional file 1). Although they had no effect on expression (Figure 2e), functional consequences of these variants could not be excluded with certainty. We therefore stably expressed the three variants separately in HEK cells. The variant transfectants showed correct immunolocalization of OATP2B1 in the plasma membrane (Figure S4A in Additional file 1). Only c.1457C > T but not c.601G > A or c.935G > A showed reduced uptake of atorvastatin, rosuvastatin and the prototypical substrate estrone sulfate (Figure S5 in Additional file 1). The calculated maximal uptake rate of atorvastatin was significantly lower for c.1457C > T and tended to be lower for rosuvastatin (Table S12 in Additional file 1). In contrast, the Km value of c.935G > A was significantly higher for atorvastatin (Table S12 in Additional file 1). Sinusoidal hepatocyte membrane immunostaining of OATP2B1 in liver cryosections from homozygous variant carriers for c.935AA was similar to OATP2B1-reference (Figure S4B in Additional file 1). Moreover, four independent computational tools did not correctly predict experimental uptake data (Table S13 in Additional file 1). Altogether, the uptake studies indicate some functional consequences, which needs validation by in vivo studies.
This first systematic analysis of the human membrane transporters OATP1B1, OATP1B3, and OATP2B1 on the interindividual variability of hepatic expression revealed a major contribution of SLCO1B1 variants on OATP1B1 protein expression. Expression of OATP1B3 or OATP2B1 was apparently not influenced by genetic variants. Most strikingly, the SLCO1B1 missense variant c.388A > G resulted in the strongest association with increased OATP1B1 protein expression whereas the c.521T > C variant, linked to statin-related myopathy [9, 35, 36], did not alter protein levels. This was observed for both the non-cholestatic livers (n = 117; Figure 2c, d) as well as the total liver set of 143 samples (Table S14 in Additional file 1), indicating that c.388A > G alters OATP1B1 expression independent of cholestasis. The observation that variant c.388A > G is associated with highest OATP1B1 protein expression is corroborated by our haplotype analysis since homozygous or compound heterozygous carriers of haplotypes *1b, *14, or *35, harboring c.388A > G but not c.521T > C, showed also the highest OATP1B1 protein levels. A mislocalization of OATP1B1 protein in genotyped livers for variant c.388A > G could be excluded by immunolocalization analyses (Figure S6 in Additional file 1).
The results of the liver study are confirmed by functional data of the pharmacokinetic healthy volunteer study since the *14 haplotype was associated with a significantly decreased atorvastatin plasma AUC in contrast to the *15 haplotype, harboring both c.388A > G and c.521T > C, and resulting in an increased AUC. Thus, the SLCO1B1 variant c.388A > G is an important determinant of OATP1B1 expression and function, independent of the c.521T > C variant. In line with in vitro reports [37, 38], one may suggest that the increased clearance by OATP1B1 c.388A > G is mainly caused by a higher protein expression. The increased hepatic atorvastatin uptake in c.388A > G carriers is also supported by haplotype data from previous studies indicating that only c.388A > G was associated with significant lower AUCs for the OATP1B1 substrates pravastatin and repaglinide [39–41]. Moreover, variant c.388A > G carriers showed a significantly improved response to statins measured by low-density lipoprotein cholesterol levels [42, 43] and were even protected from statin-induced side effects . Of note, however, the effect of the c.388A > G variant seems to be substrate-specific since the AUC was not altered, for example, for rosuvastatin , underscoring the requirement to perform pharmacokinetic studies for each OATP1B1 drug separately. Mechanistically, we suggest that variant c.388A > G modifies mRNA secondary structure, resulting in an alteration of translation efficiency as previously shown for the CFTR membrane protein . Indeed, computational theoretical modeling provided evidence that the SLCO1B1 mRNA secondary structures are altered only by haplotypes *1b, *14, and *35 harboring the c.388A > G variant (Figure S7 in Additional file 1).
In line with the localization of the OATP1B1*15 protein in the cell membrane using stably expressing HEK cells , a mislocalization of the OATP1B1 protein in livers genotyped for *15 haplotype was not found. The increased atorvastatin AUC in carriers of the *15 haplotype in our pharmacokinetic study revealed impaired atorvastatin uptake, indicating that the variant OATP1B1*15 protein is associated with decreased intrinsic transport activity. This observation is supported by previous studies using oocytes that revealed significantly reduced atorvastatin uptake by OATP1B1*15 in comparison with the reference sequence .
Another novel observation of our study is the coordinated expression of OATP1B1, OATP1B3, and OATP2B1 in human liver. The coordinate expression may be explained by regulatory networks considering previously identified transcription factors like HNF1α, Sp1, AhR, LXRα, FXR, CAR, and HNF3β [14–21]. Since HNF1α confers basal promoter activity of SLCO1B1 and SLCO1B3 and functional binding sites have been detected in the promoter regions of both genes [14, 17], we analyzed the impact of HNF1α on SLCO mRNA expression. Because exon_1e transcripts of SLCO2B1 are highly abundant in human liver  and the exon_1e promoter region has so far not been analyzed, we identified three high-scoring putative HNF1α binding sites in the exon_1e promoter (Methods and Figure S8A in Additional file 1) by in silico analysis. Electromobility shift assays confirmed in vitro binding of HNF1α to each of the three identified motifs, thereby indicating that the exon_1e transcript of SLCO2B1 is regulated by HNF1α in liver. Binding of HNF1α to any of the three sites in the exon_1e promoter of SLCO2B1 appeared to be weaker than binding to the respective motifs in the SLCO1B1 and SLCO1B3 gene promoters (Figure S8B in Additional file 1).
Among several clinical and demographic factors, including age, sex, alcohol consumption, smoking habit, and presurgery medication, only cholestasis resulted in significantly reduced OATP1B1 and OATP1B3 protein levels considering the total set of 143 liver samples (Table 1). This is in line with previous data since cholestasis in cases of primary biliary cirrhosis or progressive familial intrahepatic cholestasis is associated with reduced OATP1B1 and OATP1B3 expression  and the concerted down-regulation of both bile salt uptake transporters is considered as a protective mechanism against hepatocellular injury caused by cytotoxic bile acids. Cholestasis-related down-regulation of OATP1B1 and OATP1B3 might be of clinical relevance regarding drug response to several well-established OATP substrates, for example, lopinavir  and irinotecan .
Moreover, one aim of our study was to elucidate systematically the contribution of genetic, non-genetic and regulatory factors for the prediction of the interindividual variability of the expression of hepatic OATP transporters. Generally, the interindividual variability of expression of hepatic OATPs is considerably higher than variation of the hepatic intrinsic clearance of drugs that are substrates for OATP transport proteins as reported by clinical studies . This discrepancy is, however, not surprising since the hepatic clearance is the sum of a number of processes and factors - for example, involvement of different drug transporters for one substrate drug, short-term regulation of transporters (for example, by protein kinases), differences in retrieval of transporters from the plasma membrane, and multiple binding sites on transporters. Our multivariate analyses only using non-cholestatic liver samples revealed that the combination of genetic, non-genetic, and transcription factors explained 59% and 55% of variability of OATP1B1 and OATP1B3 protein expression, respectively, while OATP2B1 protein variance remained largely unaffected (24%). Several reasons might explain the poor prediction of interindividual variability of hepatic OATP2B1 expression, although systematic ascertainment of covariates in our liver bank was guaranteed  (Table S1 in Additional file 1). Other non-genetic factors like cytokines  may affect OATP2B1 expression. Moreover, unidentified transcription factors, genetic variation in those genes as well as epigenetics such as DNA methylation  or regulation by microRNA  may contribute to the interindividual variability of OATP2B1.
In our comprehensive work on the expression of hepatic OATPs we show for the first time a major contribution of SLCO1B1 genetics to the interindividual variability of OATP1B1 protein expression. The SLCO1B1 variant c.388A > G strongly affects OATP1B1 expression with additional functional consequences on atorvastatin plasma levels. Further work is warranted to identify underlying mechanisms for the so far unexplained interindividual variability of hepatic OATP1B3 and OATP2B1 expression.
aryl hydrocarbon receptor
area under the plasma concentration-time curve
constitutive androstane receptor
farnesoid X receptor
human embryonic kidney cells
hepatocyte nuclear factor
liver X receptor
- MALDI-TOF MS:
matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
organic anion transporting polypeptide
specificity protein 1.
We gratefully acknowledge Dr Peter Fritz, chief pathologist at the Robert-Bosch-Hospital, for expert histological examination of all liver samples, Dr Kathrin Klein for providing selected SLCO microarray data and Rabea Riedel for help in generating OATP2B1 transfectants. We greatly appreciate the expert technical help of Silvia Hübner, Ursula Waldherr, Monika Elbl, Heidi Köhler, and Igor Liebermann. This work was supported by the Robert Bosch Foundation (Stuttgart, Germany), the Federal Ministry for Education and Research (BMBF, Berlin, Germany) grant 03 IS 2061C and 0315755, the FP7-grant PITN-GA-2009-238132, and the Sigrid Jusélius Foundation (Helsinki, Finland).
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