Modeling Podocyte Biology Using Drosophila Nephrocytes

Methods Mol Biol. 2020:2067:11-24. doi: 10.1007/978-1-4939-9841-8_2.

Abstract

Vertebrate podocytes are kidney glomerular cells critically required for normal renal filtration. To fulfill their role, podocytes form molecular sieves known as slit diaphragms that contribute to the glomerular filtration barrier. The disruption of podocyte biology or slit diaphragm formation in humans is a precursor to albuminuria, renal failure, and cardiovascular morbidity. Due to genetic and functional similarities, the nephrocytes of Drosophila are increasingly used to model the genetic and metabolic basis of human podocyte biology. They have the advantage that they are a much quicker system to study compared to other murine transgenic models. In this chapter we present methods to modulate and study Drosophila nephrocyte function and diaphragm formation.

Keywords: Drosophila; Kidney; Nephrocyte; Nephropathy; Podocyte; Slit diaphragm.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Cell Culture Techniques / methods
  • Cell Membrane / metabolism
  • Cell Membrane / pathology
  • DNA-Binding Proteins / genetics
  • Disease Models, Animal
  • Drosophila melanogaster
  • Gene Expression Regulation
  • Genetic Engineering / methods
  • Humans
  • Kidney Diseases / genetics*
  • Kidney Diseases / pathology
  • Kruppel-Like Transcription Factors / genetics
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Nuclear Proteins / genetics
  • Optical Imaging / methods
  • Podocytes / cytology
  • Podocytes / metabolism
  • Podocytes / pathology*
  • Saccharomyces cerevisiae Proteins / genetics
  • Transcription Factors / genetics

Substances

  • DNA-Binding Proteins
  • GAL4 protein, S cerevisiae
  • Klf15 protein, Drosophila
  • Kruppel-Like Transcription Factors
  • Membrane Proteins
  • Nuclear Proteins
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors