Nephrotoxicity and Kidney Transport Assessment on 3D Perfused Proximal Tubules

AAPS J. 2018 Aug 14;20(5):90. doi: 10.1208/s12248-018-0248-z.

Abstract

Proximal tubules in the kidney play a crucial role in reabsorbing and eliminating substrates from the body into the urine, leading to high local concentrations of xenobiotics. This makes the proximal tubule a major target for drug toxicity that needs to be evaluated during the drug development process. Here, we describe an advanced in vitro model consisting of fully polarized renal proximal tubular epithelial cells cultured in a microfluidic system. Up to 40 leak-tight tubules were cultured on this platform that provides access to the basolateral as well as the apical side of the epithelial cells. Exposure to the nephrotoxicant cisplatin caused a dose-dependent disruption of the epithelial barrier, a decrease in viability, an increase in effluent LDH activity, and changes in expression of tight-junction marker zona-occludence 1, actin, and DNA-damage marker H2A.X, as detected by immunostaining. Activity and inhibition of the efflux pumps P-glycoprotein (P-gp) and multidrug resistance protein (MRP) were demonstrated using fluorescence-based transporter assays. In addition, the transepithelial transport function from the basolateral to the apical side of the proximal tubule was studied. The apparent permeability of the fluorescent P-gp substrate rhodamine 123 was decreased by 35% by co-incubation with cyclosporin A. Furthermore, the activity of the glucose transporter SGLT2 was demonstrated using the fluorescent glucose analog 6-NBDG which was sensitive to inhibition by phlorizin. Our results demonstrate that we developed a functional 3D perfused proximal tubule model with advanced renal epithelial characteristics that can be used for drug screening studies.

Keywords: apparent permeability (P app); kidney-on-a-chip; nephrotoxicity; proximal tubule; transepithelial transport.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / antagonists & inhibitors
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Biological Transport
  • Cell Culture Techniques*
  • Cell Line
  • Cell Polarity
  • Cisplatin / toxicity
  • Cyclosporine / toxicity
  • Dose-Response Relationship, Drug
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Humans
  • Kidney Diseases / chemically induced*
  • Kidney Diseases / metabolism
  • Kidney Diseases / pathology
  • Kidney Tubules, Proximal / drug effects*
  • Kidney Tubules, Proximal / metabolism
  • Kidney Tubules, Proximal / pathology
  • Lab-On-A-Chip Devices
  • Membrane Transport Modulators / toxicity*
  • Membrane Transport Proteins / drug effects*
  • Membrane Transport Proteins / metabolism
  • Microfluidic Analytical Techniques
  • Perfusion*
  • Phlorhizin / toxicity
  • Sodium-Glucose Transporter 2 / drug effects
  • Sodium-Glucose Transporter 2 / metabolism
  • Sodium-Glucose Transporter 2 Inhibitors / toxicity
  • Tight Junctions / drug effects
  • Tight Junctions / metabolism
  • Tight Junctions / pathology

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Membrane Transport Modulators
  • Membrane Transport Proteins
  • SLC5A2 protein, human
  • Sodium-Glucose Transporter 2
  • Sodium-Glucose Transporter 2 Inhibitors
  • Cyclosporine
  • Phlorhizin
  • Cisplatin