A novel mouse model of podocyte depletion

Nephron Exp Nephrol. 2012;121(1-2):e10-22. doi: 10.1159/000342369. Epub 2012 Oct 19.

Abstract

Aim: The goal of this study was to examine the capacity for glomerular repair after a podocyte-depleting injury.

Methods: We created transgenic (TG) mice expressing the yeast enzyme cytosine deaminase specifically in glomerular podocytes. In these TG animals, the prodrug 5-flucytosine (5-FC) is converted to 5-fluorouracil and promotes cell death.

Results: Treatment with increasing dosages of 5-FC caused graded increases in proteinuria 1-2 weeks after treatment, which returned to control levels by the 10-week time point. Light microscopic examination revealed minimal pathology at the 2-week time point, but electron microscopy revealed found foot process effacement as well as focal areas of glomerular basement membrane duplication, and immunohistochemical studies detected podocyte apoptosis and a decrease in the number of Wilms' tumor protein 1 (WT1)-positive cells. By the 10-week time point, however, the number of WT1-positive cells was similar to controls and a few mice had developed focal areas of glomerulosclerosis. Consistent with the effects of 5-FC on podocyte number, expression of the podocyte mRNAs for nephrin, podocin, synaptopodin and podocalyxin were altered in a similar temporal fashion.

Conclusion: The glomerulus has a significant capacity for repair after a podocyte-depleting injury.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acute Kidney Injury / chemically induced
  • Acute Kidney Injury / pathology*
  • Acute Kidney Injury / physiopathology*
  • Animals
  • Antimetabolites
  • Cytosine Deaminase / genetics
  • Cytosine Deaminase / metabolism
  • Disease Models, Animal*
  • Flucytosine
  • Humans
  • Kidney / drug effects
  • Kidney / pathology*
  • Kidney / physiopathology*
  • Mice
  • Mice, Transgenic
  • Podocytes / metabolism*
  • Podocytes / pathology*
  • Proteinuria / chemically induced
  • Proteinuria / pathology
  • Proteinuria / physiopathology
  • Recovery of Function

Substances

  • Antimetabolites
  • Flucytosine
  • Cytosine Deaminase