Application of RPTEC/TERT1 cells for investigation of repeat dose nephrotoxicity: A transcriptomic study

Lydia Aschauer, Alice Limonciel, Anja Wilmes, Sven Stanzel, Annette Kopp-Schneider, Philip Hewitt, Arno Lukas, Martin O Leonard, Walter Pfaller, Paul Jennings

Research output: Contribution to JournalArticleAcademicpeer-review


The kidney is a major target organ for toxicity. Incidence of chronic kidney disease (CKD) is increasing at an alarming rate due to factors such as increasing population age and increased prevalence of heart disease and diabetes. There is a major effort ongoing to develop superior predictive models of renal injury and early renal biomarkers that can predict onset of CKD. In the EU FP7 funded project, Predict-IV, we investigated the human renal proximal tubule cells line, RPTEC/TERT1 for their applicability to long term nephrotoxic mechanistic studies. To this end, we used a tiered strategy to optimise dosing regimes for 9 nephrotoxins. Our final testing protocol utilised differentiated RPTEC/TERT1 cells cultured on filter inserts treated with compounds at both the apical and basolateral side, at concentrations not exceeding IC10, for 14 days in a 24 h repeat application. Transepithelial electrical resistance and supernatant lactate were measured over the duration of the experiments and genome wide transcriptomic profiles were assayed at day 1, 3 and 14. The effect of hypoxia was investigated for a subset of compounds. The transcriptomic data were analysed to investigate compound-specific effects, global responses and mechanistically informative signatures. In addition, several potential clinically useful renal injury biomarkers were identified.

Original languageEnglish
Pages (from-to)106-116
Number of pages11
JournalToxicology in Vitro
Issue number1 Pt A
Publication statusPublished - 25 Dec 2015
Externally publishedYes


  • Cell Culture Techniques
  • Cell Line
  • Electric Impedance
  • Gene Expression Regulation
  • Humans
  • Kidney Diseases
  • Kidney Tubules, Proximal
  • Lactates
  • Pharmaceutical Preparations
  • Transcriptome
  • Journal Article
  • Research Support, Non-U.S. Gov't


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