Perturbations in homocysteine-linked redox homeostasis in a murine model for hyperhomocysteinemia

Victor Vitvitsky, Sanjana Dayal, Sally Stabler, You Zhou, Hong Wang, Steven R. Lentz, Ruma Banerjee

Research output: Contribution to journalArticle

83 Citations (Scopus)

Abstract

Elevated plasma levels of homocysteine are a risk factor for cardiovascular diseases, neural tube defects, and Alzheimer's disease. The transsulfuration pathway converts homocysteine to cysteine, and ≈50% of the cysteine in glutathione is derived from homocysteine in human liver cells, which suggests the hypothesis that defects in the transsulfuration pathway perturb redox homeostasis. To test this hypothesis, we examined a murine model for hyperhomocysteinemia in which the gene encoding the first enzyme in the transsulfuration pathway, cystathionine β-synthase (CBS), has been disrupted. Limited metabolite profiling and CBS expression studies in liver, kidney, and brain reveal tissue-specific differences in the response to Cbs disruption. Homozygous disruption of Cbs lowered cysteine concentration in all three organs. Glutathione concentration was diminished in liver and brain, thus affecting the redox buffering capacity in these organs, whereas the approximately twofold higher glutathione synthesis capacity in kidney helped preserve the glutathione pool size despite loss of the transsulfuration pathway in this organ. In contrast, disruption of a single Cbs allele elicited only minor redox perturbations. Furthermore, the Cbs+/- genotype did not confer a significant disadvantage compared with the Cbs+/+ genotype in hepatocytes challenged by oxidative stress from exposure to tertiary butylhydroperoxide. These studies provide evidence that homozygous disruption of Cbs perturbs redox homeostasis and reduces cysteine levels, raising the possibility that these changes may be important in the etiology of the clinical manifestations of CBS deficiency.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Volume287
Issue number1 56-1
DOIs
StatePublished - Jul 1 2004

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Hyperhomocysteinemia
Homocysteine
Oxidation-Reduction
Glutathione
Cysteine
Homeostasis
Liver
Genotype
Cystathionine
Homocystinuria
Kidney
tert-Butylhydroperoxide
Neural Tube Defects
Brain
Hepatocytes
Alzheimer Disease
Oxidative Stress
Cardiovascular Diseases
Alleles
Enzymes

Keywords

  • Cystathionine β-synthase
  • Cysteine
  • Glutathione
  • Homocystinuria

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)

Cite this

Perturbations in homocysteine-linked redox homeostasis in a murine model for hyperhomocysteinemia. / Vitvitsky, Victor; Dayal, Sanjana; Stabler, Sally; Zhou, You; Wang, Hong; Lentz, Steven R.; Banerjee, Ruma.

In: American Journal of Physiology - Regulatory Integrative and Comparative Physiology, Vol. 287, No. 1 56-1, 01.07.2004.

Research output: Contribution to journalArticle

Vitvitsky, Victor ; Dayal, Sanjana ; Stabler, Sally ; Zhou, You ; Wang, Hong ; Lentz, Steven R. ; Banerjee, Ruma. / Perturbations in homocysteine-linked redox homeostasis in a murine model for hyperhomocysteinemia. In: American Journal of Physiology - Regulatory Integrative and Comparative Physiology. 2004 ; Vol. 287, No. 1 56-1.
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