Granulocyte function in patients with L-ferritin iron-responsive element (IRE) 39C-->T-positive hereditary hyperferritinaemia-cataract syndrome

Eur J Clin Invest. 2004 Oct;34(10):701-8. doi: 10.1111/j.1365-2362.2004.01408.x.

Abstract

Background: Hereditary hyperferritinaemia-cataract syndrome (HHCS) is an autosomal dominant trait associated with mutations in the iron responsive element (IRE) of the ferritin light-chain (L-ferritin) gene. Patients typically show elevated serum ferritin concentrations without iron overload and a bilateral cataract. Hyperferritinaemia can be associated with granulocyte dysfunction in patients with thalassemia beta and in haemodialysis patients. The effect of increased L-ferritin levels on granulocyte function in patients with HHCS is unknown.

Material and methods: We examined glucose uptake, oxidative burst, chemotaxis, phagocytosis, apoptosis and intracellular calcium concentrations in polymorphonuclear leucocytes (PMNLs) of five affected members of a family with HHCS and in five healthy individuals matched for age and gender.

Results: Mutation testing revealed a 39C-->T transition in IRE in all five patients with HHCS. Serum ferritin levels of patients ranged between 907 and 2030 microg L(-1), respectively. In comparison with healthy individuals, PMNLs of patients with HHCS showed a significant increase in PMA-mediated stimulation of the oxidative burst, as well as a significantly higher stimulation of glucose uptake but no difference with respect to chemotaxis, phagocytosis, apoptosis and intracellular calcium concentrations.

Conclusion: In summary, our study suggests that hyperferritinaemia in patients with IRE 39C-->T-positive HHCS is associated with activation of PMNLs but not with disturbance of fundamental PMNL function.

MeSH terms

  • Adolescent
  • Adult
  • Apoptosis
  • Cataract / blood
  • Cataract / genetics*
  • Chemotaxis, Leukocyte
  • Female
  • Ferritins / blood*
  • Glucose / metabolism
  • Granulocytes / physiology*
  • Humans
  • Iron Metabolism Disorders / genetics*
  • Iron Metabolism Disorders / metabolism
  • Male
  • Middle Aged
  • Neutrophils / metabolism
  • Pedigree
  • Phagocytosis
  • Respiratory Burst
  • Syndrome

Substances

  • Ferritins
  • Glucose