A Comprehensive Analysis of Ontogeny of Renal Drug Transporters: mRNA Analyses, Quantitative Proteomics, and Localization. Issue 5 (3rd July 2019)

• Record Type: Journal Article
• Authors: Cheung, Kit Wun Kathy; van Groen, Bianca D.; Spaans, Edwin; van Borselen, Marjolein D.; de Bruijn, Adrianus C.J.M.; Simons‐Oosterhuis, Ytje; Tibboel, Dick; Samsom, Janneke N.; Verdijk, Robert M.; Smeets, Bart; Zhang, Lei; Huang, Shiew‐Mei; Giacomini, Kathleen M.; de Wildt, Saskia N.
• Is Part Of: Clinical pharmacology & therapeutics. Volume 106:Issue 5(2019)
• Page Start: 1083
• Page End: 1092
• Publication Date: 2019-07-03
• Subjects: Pharmacology -- Periodicals; Therapeutics -- Periodicals; 615.5
• DOI: 10.1002/cpt.1516
• Languages: English
• ISSNs: 0009-9236

Abstract

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.