Screening of Drug-Transporter Interactions in a 3D Microfluidic Renal Proximal Tubule on a Chip

AAPS J. 2018 Jul 26;20(5):87. doi: 10.1208/s12248-018-0247-0.

Abstract

Drug-transporter interactions could impact renal drug clearance and should ideally be detected in early stages of drug development to avoid toxicity-related withdrawals in later stages. This requires reliable and robust assays for which current high-throughput screenings have, however, poor predictability. Kidney-on-a-chip platforms have the potential to improve predictability, but often lack compatibility with high-content detection platforms. Here, we combined conditionally immortalized proximal tubule epithelial cells overexpressing organic anion transporter 1 (ciPTEC-OAT1) with the microfluidic titer plate OrganoPlate to develop a screenings assay for renal drug-transporter interactions. In this platform, apical localization of F-actin and intracellular tight-junction protein zonula occludens-1 (ZO-1) indicated appropriate cell polarization. Gene expression levels of the drug transporters organic anion transporter 1 (OAT1; SLC22A6), organic cation transporter 2 (OCT2; SLC22A2), P-glycoprotein (P-gp; ABCB1), and multidrug resistance-associated protein 2 and 4 (MRP2/4; ABCC2/4) were similar levels to 2D static cultures. Functionality of the efflux transporters P-gp and MRP2/4 was studied as proof-of-concept for 3D assays using calcein-AM and 5-chloromethylfluorescein-diacetate (CMFDA), respectively. Confocal imaging demonstrated a 4.4 ± 0.2-fold increase in calcein accumulation upon P-gp inhibition using PSC833. For MRP2/4, a 3.0 ± 0.2-fold increased accumulation of glutathione-methylfluorescein (GS-MF) was observed upon inhibition with a combination of PSC833, MK571, and KO143. Semi-quantitative image processing methods for P-gp and MRP2/4 was demonstrated with corresponding Z'-factors of 0.1 ± 0.3 and 0.4 ± 0.1, respectively. In conclusion, we demonstrate a 3D microfluidic PTEC model valuable for screening of drug-transporter interactions that further allows multiplexing of endpoint read-outs for drug-transporter interactions and toxicity.

Keywords: Drug screening; Drug-transporter interaction; Efflux transport; Microfluidics; Nephrotoxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Biological Transport
  • Cell Line, Transformed
  • Cell Polarity
  • Drug Evaluation, Preclinical / methods*
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Humans
  • Kidney Tubules, Proximal / drug effects*
  • Kidney Tubules, Proximal / metabolism
  • Lab-On-A-Chip Devices*
  • Membrane Transport Modulators / toxicity*
  • Membrane Transport Proteins / drug effects*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • Microfluidic Analytical Techniques / instrumentation*
  • Microscopy, Confocal
  • Multidrug Resistance-Associated Protein 2
  • Risk Assessment
  • Zonula Occludens-1 Protein / metabolism

Substances

  • ABCC2 protein, human
  • Actins
  • Membrane Transport Modulators
  • Membrane Transport Proteins
  • Multidrug Resistance-Associated Protein 2
  • TJP1 protein, human
  • Zonula Occludens-1 Protein