학술논문

A Comprehensive Analysis of Ontogeny of Renal Drug Transporters: mRNA Analyses, Quantitative Proteomics, and Localization
Document Type
article
Source
Clinical Pharmacology & Therapeutics. 106(5)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Cancer
Kidney Disease
Prevention
Antimicrobial Resistance
1.1 Normal biological development and functioning
5.1 Pharmaceuticals
Development of treatments and therapeutic interventions
Underpinning research
Generic health relevance
Adolescent
Adult
Age Factors
Aged
Child
Child
Preschool
Chromatography
Liquid
Female
Humans
Infant
Infant
Newborn
Kidney Cortex
Male
Membrane Transport Proteins
Middle Aged
Pregnane X Receptor
Proteomics
RNA
Messenger
Real-Time Polymerase Chain Reaction
Tandem Mass Spectrometry
Young Adult
Pharmacology and Pharmaceutical Sciences
Pharmacology & Pharmacy
Pharmacology and pharmaceutical sciences
Language
Abstract
Human renal membrane transporters play key roles in the disposition of renally cleared drugs and endogenous substrates, but their ontogeny is largely unknown. Using 184 human postmortem frozen renal cortical tissues (preterm newborns to adults) and a subset of 62 tissue samples, we measured the mRNA levels of 11 renal transporters and the transcription factor pregnane X receptor (PXR) with quantitative real-time polymerase chain reaction, and protein abundance of nine transporters using liquid chromatography tandem mass spectrometry selective reaction monitoring, respectively. Expression levels of p-glycoprotein, urate transporter 1, organic anion transporter 1, organic anion transporter 3, and organic cation transporter 2 increased with age. Protein levels of multidrug and toxin extrusion transporter 2-K and breast cancer resistance protein showed no difference from newborns to adults, despite age-related changes in mRNA expression. Multidrug and toxin extrusion transporter 1, glucose transporter 2, multidrug resistance-associated protein 2, multidrug resistance-associated protein 4 (MRP4), and PXR expression levels were stable. Using immunohistochemistry, we found that MRP4 localization in pediatric samples was similar to that in adult samples. Collectively, our study revealed that renal drug transporters exhibited different rates and patterns of maturation, suggesting that renal handling of substrates may change with age.