A new method for the enrichment of single renal proximal tubular cells and their first use in the comet assay

Mutat Res. 1997 Sep 18;393(1-2):175-8. doi: 10.1016/s1383-5718(97)00106-x.

Abstract

A protocol was developed to isolate and enrich single renal proximal tubular cells, performing the following steps: in situ kidney perfusion; isolation of renal tissue pieces by collagenase digestion; selective enrichment of proximal tubular fragments by Percoll gradient centrifugation; and isolation of single proximal tubular cells by digestion of proximal tubular fragments with trypsin. The mean enrichment rate, determined by the glucose-6-phosphatase staining method, was 78.9% with a mean cell viability of 93.8%. After modification of the comet assay protocol, genotoxicity in proximal tubular cells could be investigated. A dose-dependent genotoxic effect of ethyl methanesulphonate in these cells was proven.

MeSH terms

  • Animals
  • Cell Separation / methods*
  • DNA / drug effects
  • DNA / isolation & purification
  • DNA Damage
  • Electrophoresis / methods
  • Ethyl Methanesulfonate / toxicity
  • Evaluation Studies as Topic
  • In Vitro Techniques
  • Kidney Tubules, Proximal / cytology*
  • Kidney Tubules, Proximal / drug effects
  • Kidney Tubules, Proximal / metabolism
  • Male
  • Mutagenicity Tests / methods*
  • Mutagens / toxicity
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Mutagens
  • DNA
  • Ethyl Methanesulfonate