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 inInternational journal of molecular sciences Vol. 20; no. 21; p. 5303
Main Authors Oswald, Stefan, Müller, Janett, Neugebauer, Ute, Schröter, Rita, Herrmann, Edwin, Pavenstädt, Hermann, Ciarimboli, Giuliano
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 24.10.2019
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ISSN1422-0067
1661-6596
1422-0067
DOI10.3390/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.
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.)
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/31653114$$D View this record in MEDLINE/PubMed
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Keywords gender
transporters
human kidneys
protein expression
age
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Snippet Renal drug transporters such as the organic cation transporters (OCTs), organic anion transporters (OATs) and multidrug resistance proteins (MRPs) play an...
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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
URI https://www.ncbi.nlm.nih.gov/pubmed/31653114
https://www.proquest.com/docview/2548661447
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https://pubmed.ncbi.nlm.nih.gov/PMC6862022
Volume 20
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