Ceruloplasmin deficiency does not induce macrophagic iron overload: lessons from a new rat model of hereditary aceruloplasminemia

FASEB J. 2019 Dec;33(12):13492-13502. doi: 10.1096/fj.201901106R. Epub 2019 Sep 27.

Abstract

Hereditary aceruloplasminemia (HA), related to mutations in the ceruloplasmin (Cp) gene, leads to iron accumulation. Ceruloplasmin ferroxidase activity being considered essential for macrophage iron release, macrophage iron overload is expected, but it is not found in hepatic and splenic macrophages in humans. Our objective was to get a better understanding of the mechanisms leading to iron excess in HA. A clustered regularly interspaced short palindromic repeats (CRISPR)/ CRISPR associated protein 9 (Cas9) knockout of the Cp gene was performed on Sprague-Dawley rats. We evaluated the iron status in plasma, the expression of iron metabolism genes, and the status of other metals whose interactions with iron are increasingly recognized. In Cp-/- rats, plasma ceruloplasmin and ferroxidase activity were absent, together with decreased iron concentration and transferrin saturation. Similarly as in humans, the hepatocytes were iron overloaded conversely to hepatic and splenic macrophages. Despite a relative hepcidin deficiency in Cp-/- rats and the loss of ferroxidase activity, potentially expected to limit the interaction of iron with transferrin, no increase of plasma non-transferrin-bound iron level was found. Copper was decreased in the spleen, whereas manganese was increased in the plasma. These data suggest that the reported role of ceruloplasmin cannot fully explain the iron hepatosplenic phenotype in HA, encouraging the search for additional mechanisms.-Kenawi, M., Rouger, E., Island, M.-L., Leroyer, P., Robin, F., Remy, S., Tesson, L., Anegon, I., Nay, K., Derbré, F., Brissot, P., Ropert, M., Cavey, T., Loréal, O. Ceruloplasmin deficiency does not induce macrophagic iron overload: lessons from a new rat model of hereditary aceruloplasminemia.

Keywords: CRISPR/Cas9; genetic disease; hepatocyte; hepcidin; metals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • CRISPR-Cas Systems
  • Ceruloplasmin / antagonists & inhibitors
  • Ceruloplasmin / deficiency*
  • Ceruloplasmin / genetics
  • Disease Models, Animal*
  • Female
  • Iron / analysis
  • Iron / metabolism*
  • Iron Metabolism Disorders / complications*
  • Iron Metabolism Disorders / genetics
  • Iron Metabolism Disorders / pathology
  • Iron Overload / etiology
  • Iron Overload / pathology*
  • Liver / metabolism
  • Liver / pathology
  • Macrophages / metabolism
  • Macrophages / pathology*
  • Male
  • Mutation
  • Neurodegenerative Diseases / complications*
  • Neurodegenerative Diseases / genetics
  • Neurodegenerative Diseases / pathology
  • Rats
  • Rats, Sprague-Dawley
  • Sequence Homology
  • Spleen / metabolism
  • Spleen / pathology

Substances

  • Iron
  • Ceruloplasmin

Supplementary concepts

  • Familial apoceruloplasmin deficiency