Glutathione synthetase deficient human fibroblasts in culture

Clin Chim Acta. 1983 Nov 30;135(1):57-64. doi: 10.1016/0009-8981(83)90388-1.

Abstract

Cultured skin fibroblasts from patients with 5-oxoprolinuria caused by hereditary deficiency of glutathione synthetase have decreased levels of the corresponding enzyme as well as of glutathione. Fibroblasts from the same patients accumulated gamma-glutamyl cysteine, but the levels were lower than those of glutathione in control fibroblasts. The uptake of [35S]cystine was equally rapid in control and patient fibroblasts. In the acid-soluble fraction gamma-glutamyl-[35S]cysteine accumulated in fibroblasts from patients but not from controls. Appreciable turnover of gamma-glutamyl cysteine and glutathione in the respective cell strains was observed, the half-lives of these pools being approximately 5 hours. The growth rate of mutant fibroblasts in culture was significantly slower than that of control fibroblasts. There was no significant accumulation of 5-oxoproline in the culture medium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Division
  • Cells, Cultured
  • Cystine / metabolism
  • Dipeptides / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / enzymology*
  • Glutathione / metabolism
  • Glutathione Synthase / deficiency*
  • Humans
  • Kinetics
  • Peptide Synthases / deficiency*

Substances

  • Dipeptides
  • Cystine
  • Peptide Synthases
  • Glutathione Synthase
  • Glutathione
  • gamma-glutamylcysteine