Renal proximal tubular cells acquire resistance to cell death stimuli in mice with hereditary tyrosinemia type 1

Kidney Int. 2004 Sep;66(3):990-1000. doi: 10.1111/j.1523-1755.2004.00788.x.

Abstract

Background: Hereditary tyrosinemia type 1 (HT1), which is associated with severe liver and kidney damage, is caused by deficiency of fumarylacetoacetate hydrolase (FAH), the last enzyme of the tyrosine breakdown cascade. HT1-associated liver and kidney failure can be prevented by blocking an enzyme upstream of FAH in the tyrosine breakdown pathway with 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC). FAH knockout mice develop the HT1 phenotype when NTBC treatment is discontinued.

Methods: The occurrence of cell death was investigated in kidneys of Fah(-/-) mice on and off NTBC either unchallenged or injected with 800 mg/kg of homogentisic acid (HGA), an intermediate of tyrosine breakdown.

Results: No cell death could be detected in kidneys of Fah(-/-) mice on NTBC. A slight increase of cleaved caspase-3 was the only apoptosis-related feature that could be detected in kidneys of Fah(-/-) mice off NTBC. Challenge of Fah(-/-) mice on NTBC with HGA led to massive death of renal proximal tubular cells, with positive terminal deoxynucleotidyl transferase-mediated deoxyuridine diphosphate (dUDP) nick-end labeling (TUNEL) and DNA fragmentation assays, but hardly any cleavage of caspase-9 and caspase-3. Fah(-/-) mice off NTBC acquired resistance to HGA-induced renal cell death and the kidneys exhibited relatively few features of apoptosis upon challenge with HGA, with a small increase in expression of cleaved caspase-9 and caspase-3.

Conclusion: Kidneys of adult Fah(-/-) mice, withdrawn from NTBC for 15 days, reveal limited characteristics of apoptosis, and have acquired resistance to a caspase-9- and caspase-3-independent form of cell death provoked by HGA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caspase 3
  • Caspase 9
  • Caspases / metabolism
  • Cyclohexanones / pharmacology
  • DNA Fragmentation / physiology*
  • Disease Models, Animal
  • Enzyme Inhibitors / pharmacology
  • Hepatocytes / transplantation
  • Homogentisic Acid / pharmacology
  • Hydrolases / genetics*
  • In Situ Nick-End Labeling
  • Kidney Tubules, Proximal / pathology*
  • Mice
  • Mice, Knockout
  • Nitrobenzoates / pharmacology
  • Survival Rate
  • Tyrosine / metabolism
  • Tyrosinemias / genetics
  • Tyrosinemias / mortality
  • Tyrosinemias / pathology*

Substances

  • Cyclohexanones
  • Enzyme Inhibitors
  • Nitrobenzoates
  • Tyrosine
  • Hydrolases
  • Casp3 protein, mouse
  • Casp9 protein, mouse
  • Caspase 3
  • Caspase 9
  • Caspases
  • fumarylacetoacetase
  • nitisinone
  • Homogentisic Acid