Targeted genomic disruption of H-ras and N-ras has no effect on early renal changes after unilateral ureteral ligation

World J Urol. 2009 Dec;27(6):787-97. doi: 10.1007/s00345-009-0399-8.

Abstract

Purpose: To assess the contribution of two different Ras monomeric GTPases isoforms H- and N-Ras in the early changes associated to obstructive nephropathy induced by unilateral ureteral obstruction (UUO).

Methods: UUO was performed in N-ras (N-ras−/−) and H-ras (H-ras−/−) knock-out mice and control (H-ras+/+/N-ras+/+) mice of C57Bl/6 background. Fibronectin, α-smooth muscle actin, cleaved caspase-3, ki-67, Ras-GTP, pERK, and pAkt expression was analyzed by western blot and/or immunohistochemistry. Ras isoforms activation and caspase activity were determined by both western blot and ELISA.

Results: Three days after UUO, obstructed (O) kidneys of H-ras−/−, N-ras−/−and H-ras+/+/N-ras+/+mice showed no significant differences in activated total ras, pERK1/2, pAkt, total Akt levels, fibronectin, α-SMA expression, cell proliferation, and activated caspase-3. The morphological alterations in the O kidneys, revealed by histological and immunohistochemical studies, were also similar in H-ras−/−, N-ras−/−, and H-ras+/+/N-ras+/+mice.

Conclusions: These data suggest that the activation of H-ras and N-ras isoforms does not play a major role in the early renal damage induced by UUO.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Caspase 3 / metabolism
  • Disease Models, Animal
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Fibronectins / metabolism
  • Fibrosis
  • Genome
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney Diseases / pathology
  • Kidney Diseases / physiopathology*
  • Ligation
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins p21(ras) / genetics*
  • Proto-Oncogene Proteins p21(ras) / metabolism*
  • Ureter / physiology*
  • Ureteral Obstruction / pathology
  • Ureteral Obstruction / physiopathology*

Substances

  • Actins
  • Fibronectins
  • Proto-Oncogene Proteins c-akt
  • Extracellular Signal-Regulated MAP Kinases
  • Casp3 protein, mouse
  • Caspase 3
  • Proto-Oncogene Proteins p21(ras)