Expression of xenobiotic transporters in the human renal proximal tubule cell line RPTEC/TERT1
L Aschauer, G Carta, N Vogelsang, E Schlatter… - Toxicology in Vitro, 2015 - Elsevier
L Aschauer, G Carta, N Vogelsang, E Schlatter, P Jennings
Toxicology in Vitro, 2015•ElsevierThe kidney is a major target for drug-induced injury, primarily due the fact that it transports a
wide variety of chemical entities into and out of the tubular lumen. Here, we investigated the
expression of the main xenobiotic transporters in the human renal proximal tubule cell line
RPTEC/TERT1 at an mRNA and/or protein level. RPTEC/TERT1 cells expressed OCT2,
OCT3, OCTN2, MATE1, MATE2, OAT1, OAT3 and OAT4. The functionality of the OCTs was
demonstrated by directional transport of the fluorescent dye 4-Di-1-ASP. In addition, P …
wide variety of chemical entities into and out of the tubular lumen. Here, we investigated the
expression of the main xenobiotic transporters in the human renal proximal tubule cell line
RPTEC/TERT1 at an mRNA and/or protein level. RPTEC/TERT1 cells expressed OCT2,
OCT3, OCTN2, MATE1, MATE2, OAT1, OAT3 and OAT4. The functionality of the OCTs was
demonstrated by directional transport of the fluorescent dye 4-Di-1-ASP. In addition, P …
Abstract
The kidney is a major target for drug-induced injury, primarily due the fact that it transports a wide variety of chemical entities into and out of the tubular lumen. Here, we investigated the expression of the main xenobiotic transporters in the human renal proximal tubule cell line RPTEC/TERT1 at an mRNA and/or protein level. RPTEC/TERT1 cells expressed OCT2, OCT3, OCTN2, MATE1, MATE2, OAT1, OAT3 and OAT4. The functionality of the OCTs was demonstrated by directional transport of the fluorescent dye 4-Di-1-ASP. In addition, P-glycoprotein activity in RPTEC/TERT1 cells was verified by fluorescent dye retention in presence of various P-glycoprotein inhibitors. In comparison to proliferating cells, contact inhibited RPTEC/TERT1 cells expressed increased mRNA levels of several ABC transporter family members and were less sensitive to cyclosporine A. We conclude that differentiated RPTEC/TERT1 cells are well suited for utilisation in xenobiotic transport and pharmacokinetic studies.
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