Protein Abundance of Clinically Relevant Drug Transporters in The Human Kidneys
Renal drug transporters such as the organic cation transporters (OCTs), organic anion transporters (OATs) and multidrug resistance proteins (MRPs) play an important role in the tubular secretion of many drugs influencing their efficacy and safety. However, only little is known about the distinct pro...
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Published in | International journal of molecular sciences Vol. 20; no. 21; p. 5303 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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24.10.2019
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ISSN | 1422-0067 1661-6596 1422-0067 |
DOI | 10.3390/ijms20215303 |
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Abstract | Renal drug transporters such as the organic cation transporters (OCTs), organic anion transporters (OATs) and multidrug resistance proteins (MRPs) play an important role in the tubular secretion of many drugs influencing their efficacy and safety. However, only little is known about the distinct protein abundance of these transporters in human kidneys, and about the impact of age and gender as potential factors of inter-subject variability in their expression and function. The aim of this study was to determine the protein abundance of MDR1, MRP1-4, BCRP, OAT1-3, OCT2-3, MATE1, PEPT1/2, and ORCTL2 by liquid chromatography-tandem mass spectrometry-based targeted proteomics in a set of 36 human cortex kidney samples (20 males, 16 females; median age 53 and 55 years, respectively). OAT1 and 3, OCT2 and ORCTL2 were found to be most abundant renal SLC transporters while MDR1, MRP1 and MRP4 were the dominating ABC transporters. Only the expression levels of MDR1 and ORCTL2 were significantly higher abundant in older donors. Moreover, we found several significant correlations between different transporters, which may indicate their functional interplay in renal vectorial transport processes. Our data may contribute to a better understanding of the molecular processes determining renal excretion of drugs. |
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AbstractList | Renal drug transporters such as the organic cation transporters (OCTs), organic anion transporters (OATs) and multidrug resistance proteins (MRPs) play an important role in the tubular secretion of many drugs influencing their efficacy and safety. However, only little is known about the distinct protein abundance of these transporters in human kidneys, and about the impact of age and gender as potential factors of inter-subject variability in their expression and function. The aim of this study was to determine the protein abundance of MDR1, MRP1-4, BCRP, OAT1-3, OCT2-3, MATE1, PEPT1/2, and ORCTL2 by liquid chromatography-tandem mass spectrometry-based targeted proteomics in a set of 36 human cortex kidney samples (20 males, 16 females; median age 53 and 55 years, respectively). OAT1 and 3, OCT2 and ORCTL2 were found to be most abundant renal SLC transporters while MDR1, MRP1 and MRP4 were the dominating ABC transporters. Only the expression levels of MDR1 and ORCTL2 were significantly higher abundant in older donors. Moreover, we found several significant correlations between different transporters, which may indicate their functional interplay in renal vectorial transport processes. Our data may contribute to a better understanding of the molecular processes determining renal excretion of drugs. Renal drug transporters such as the organic cation transporters (OCTs), organic anion transporters (OATs) and multidrug resistance proteins (MRPs) play an important role in the tubular secretion of many drugs influencing their efficacy and safety. However, only little is known about the distinct protein abundance of these transporters in human kidneys, and about the impact of age and gender as potential factors of inter-subject variability in their expression and function. The aim of this study was to determine the protein abundance of MDR1, MRP1-4, BCRP, OAT1-3, OCT2-3, MATE1, PEPT1/2, and ORCTL2 by liquid chromatography-tandem mass spectrometry-based targeted proteomics in a set of 36 human cortex kidney samples (20 males, 16 females; median age 53 and 55 years, respectively). OAT1 and 3, OCT2 and ORCTL2 were found to be most abundant renal SLC transporters while MDR1, MRP1 and MRP4 were the dominating ABC transporters. Only the expression levels of MDR1 and ORCTL2 were significantly higher abundant in older donors. Moreover, we found several significant correlations between different transporters, which may indicate their functional interplay in renal vectorial transport processes. Our data may contribute to a better understanding of the molecular processes determining renal excretion of drugs.Renal drug transporters such as the organic cation transporters (OCTs), organic anion transporters (OATs) and multidrug resistance proteins (MRPs) play an important role in the tubular secretion of many drugs influencing their efficacy and safety. However, only little is known about the distinct protein abundance of these transporters in human kidneys, and about the impact of age and gender as potential factors of inter-subject variability in their expression and function. The aim of this study was to determine the protein abundance of MDR1, MRP1-4, BCRP, OAT1-3, OCT2-3, MATE1, PEPT1/2, and ORCTL2 by liquid chromatography-tandem mass spectrometry-based targeted proteomics in a set of 36 human cortex kidney samples (20 males, 16 females; median age 53 and 55 years, respectively). OAT1 and 3, OCT2 and ORCTL2 were found to be most abundant renal SLC transporters while MDR1, MRP1 and MRP4 were the dominating ABC transporters. Only the expression levels of MDR1 and ORCTL2 were significantly higher abundant in older donors. Moreover, we found several significant correlations between different transporters, which may indicate their functional interplay in renal vectorial transport processes. Our data may contribute to a better understanding of the molecular processes determining renal excretion of drugs. |
Author | Müller, Janett Ciarimboli, Giuliano Neugebauer, Ute Oswald, Stefan Pavenstädt, Hermann Herrmann, Edwin Schröter, Rita |
AuthorAffiliation | 1 Department of Clinical Pharmacology, University Medicine of Greifswald, 17475 Greifswald, Germany; nettie.m@web.de 3 Urology Clinic, University Hospital of Münster, 48149 Münster, Germany; edwin.herrmann@prosper-hospital.de 2 Medicine Clinic D, Experimental Nephrology, University Hospital of Münster, 48149 Münster, Germany; Ute.Neugebauer@uni-muenster.de (U.N.); ritas@uni-muenster.de (R.S.); Hermann.Pavenstaedt@ukmuenster.de (H.P.) |
AuthorAffiliation_xml | – name: 1 Department of Clinical Pharmacology, University Medicine of Greifswald, 17475 Greifswald, Germany; nettie.m@web.de – name: 3 Urology Clinic, University Hospital of Münster, 48149 Münster, Germany; edwin.herrmann@prosper-hospital.de – name: 2 Medicine Clinic D, Experimental Nephrology, University Hospital of Münster, 48149 Münster, Germany; Ute.Neugebauer@uni-muenster.de (U.N.); ritas@uni-muenster.de (R.S.); Hermann.Pavenstaedt@ukmuenster.de (H.P.) |
Author_xml | – sequence: 1 givenname: Stefan orcidid: 0000-0001-6269-4368 surname: Oswald fullname: Oswald, Stefan – sequence: 2 givenname: Janett surname: Müller fullname: Müller, Janett – sequence: 3 givenname: Ute surname: Neugebauer fullname: Neugebauer, Ute – sequence: 4 givenname: Rita surname: Schröter fullname: Schröter, Rita – sequence: 5 givenname: Edwin surname: Herrmann fullname: Herrmann, Edwin – sequence: 6 givenname: Hermann surname: Pavenstädt fullname: Pavenstädt, Hermann – sequence: 7 givenname: Giuliano orcidid: 0000-0002-4365-3656 surname: Ciarimboli fullname: Ciarimboli, Giuliano |
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SubjectTerms | ABC transporters Adult Age Age Factors Aged ATP Binding Cassette Transporter, Subfamily G, Member 2 - genetics ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism Chromatography Chromatography, High Pressure Liquid Drugs Female Gender Homeostasis Humans Kidney Cortex - metabolism Kidneys Male Mass spectrometry Middle Aged Organic Anion Transport Protein 1 - genetics Organic Anion Transport Protein 1 - metabolism Organic Cation Transport Proteins - genetics Organic Cation Transport Proteins - metabolism Organic Cation Transporter 2 - genetics Organic Cation Transporter 2 - metabolism Physiology Plasma Protein expression Proteins Proteome - analysis Proteomics Scientific imaging Sex Factors Tandem Mass Spectrometry Urine |
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Title | Protein Abundance of Clinically Relevant Drug Transporters in The Human Kidneys |
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