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Interindividual Diversity in Expression of Organic Anion Uptake Transporters in Normal and Cirrhotic Human Liver

The liver plays an essential role in removing endogenous and exogenous compounds from the circulation. This function is mediated by specific transporters, including members of the family of organic anion transport proteins (OATPs) and the Na(+)‐taurocholate transporting polypeptide (NTCP). In the pr...

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Autores principales: Taniguchi, Tatsuya, Zanetti‐Yabur, Alana, Wang, Pijun, Usyk, Mykhaylo, Burk, Robert D., Wolkoff, Allan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193130/
https://www.ncbi.nlm.nih.gov/pubmed/32363323
http://dx.doi.org/10.1002/hep4.1489
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author Taniguchi, Tatsuya
Zanetti‐Yabur, Alana
Wang, Pijun
Usyk, Mykhaylo
Burk, Robert D.
Wolkoff, Allan W.
author_facet Taniguchi, Tatsuya
Zanetti‐Yabur, Alana
Wang, Pijun
Usyk, Mykhaylo
Burk, Robert D.
Wolkoff, Allan W.
author_sort Taniguchi, Tatsuya
collection PubMed
description The liver plays an essential role in removing endogenous and exogenous compounds from the circulation. This function is mediated by specific transporters, including members of the family of organic anion transport proteins (OATPs) and the Na(+)‐taurocholate transporting polypeptide (NTCP). In the present study, transporter protein expression was determined in liver samples from patients with cirrhosis or controls without liver disease. Five transporters (OATP1A2, OATP1B1, OATP1B3, OATP2B1, and NTCP) were studied. Transporter content in homogenates of human liver was quantified on western blots probed with transporter‐specific antibodies in which a calibrated green fluorescent protein‐tagged transporter standard was included. Liver samples from 21 patients with cirrhosis (hepatitis C in 17 and alcohol abuse in 4) and 17 controls without liver disease were analyzed. Expression of each of the transporters had a large spread, varying by an order of magnitude in cirrhotic and control livers. OATP1B1 was the most abundant transporter in controls (P < 0.01) but was significantly lower in cirrhotic livers as was NTCP expression (P < 0.01). There was little difference in transporter expression with respect to age or sex. Despite the large variability in transporter expression within a group, analysis in individuals showed that those with high or low expression of one transporter had a similar magnitude in expression of the others. Conclusion: Differences in transporter expression could explain unanticipated heterogeneity of drug transport and metabolism in individuals with and without liver disease.
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spelling pubmed-71931302020-05-01 Interindividual Diversity in Expression of Organic Anion Uptake Transporters in Normal and Cirrhotic Human Liver Taniguchi, Tatsuya Zanetti‐Yabur, Alana Wang, Pijun Usyk, Mykhaylo Burk, Robert D. Wolkoff, Allan W. Hepatol Commun Original Articles The liver plays an essential role in removing endogenous and exogenous compounds from the circulation. This function is mediated by specific transporters, including members of the family of organic anion transport proteins (OATPs) and the Na(+)‐taurocholate transporting polypeptide (NTCP). In the present study, transporter protein expression was determined in liver samples from patients with cirrhosis or controls without liver disease. Five transporters (OATP1A2, OATP1B1, OATP1B3, OATP2B1, and NTCP) were studied. Transporter content in homogenates of human liver was quantified on western blots probed with transporter‐specific antibodies in which a calibrated green fluorescent protein‐tagged transporter standard was included. Liver samples from 21 patients with cirrhosis (hepatitis C in 17 and alcohol abuse in 4) and 17 controls without liver disease were analyzed. Expression of each of the transporters had a large spread, varying by an order of magnitude in cirrhotic and control livers. OATP1B1 was the most abundant transporter in controls (P < 0.01) but was significantly lower in cirrhotic livers as was NTCP expression (P < 0.01). There was little difference in transporter expression with respect to age or sex. Despite the large variability in transporter expression within a group, analysis in individuals showed that those with high or low expression of one transporter had a similar magnitude in expression of the others. Conclusion: Differences in transporter expression could explain unanticipated heterogeneity of drug transport and metabolism in individuals with and without liver disease. John Wiley and Sons Inc. 2020-03-11 /pmc/articles/PMC7193130/ /pubmed/32363323 http://dx.doi.org/10.1002/hep4.1489 Text en © 2020 The Authors. Hepatology Communications published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Taniguchi, Tatsuya
Zanetti‐Yabur, Alana
Wang, Pijun
Usyk, Mykhaylo
Burk, Robert D.
Wolkoff, Allan W.
Interindividual Diversity in Expression of Organic Anion Uptake Transporters in Normal and Cirrhotic Human Liver
title Interindividual Diversity in Expression of Organic Anion Uptake Transporters in Normal and Cirrhotic Human Liver
title_full Interindividual Diversity in Expression of Organic Anion Uptake Transporters in Normal and Cirrhotic Human Liver
title_fullStr Interindividual Diversity in Expression of Organic Anion Uptake Transporters in Normal and Cirrhotic Human Liver
title_full_unstemmed Interindividual Diversity in Expression of Organic Anion Uptake Transporters in Normal and Cirrhotic Human Liver
title_short Interindividual Diversity in Expression of Organic Anion Uptake Transporters in Normal and Cirrhotic Human Liver
title_sort interindividual diversity in expression of organic anion uptake transporters in normal and cirrhotic human liver
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193130/
https://www.ncbi.nlm.nih.gov/pubmed/32363323
http://dx.doi.org/10.1002/hep4.1489
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