Mycobacteria-induced anaemia revisited: a molecular approach reveals the involvement of NRAMP1 and lipocalin-2, but not of hepcidin

Immunobiology. 2011 Oct;216(10):1127-34. doi: 10.1016/j.imbio.2011.04.004. Epub 2011 Apr 20.

Abstract

Anaemia is a frequent complication of chronic infectious diseases but the exact mechanisms by which it develops remain to be clarified. In the present work, we used a mouse model of mycobacterial infection to study molecular alterations of iron metabolism induced by infection. We show that four weeks after infection with Mycobacterium avium BALB/c mice exhibited a moderate anaemia, which was not accompanied by an increase on hepatic hepcidin mRNA expression. Instead, infected mice presented increased mRNA expression of ferroportin (Slc40a1), ceruloplasmin (Cp), hemopexin (Hpx), heme-oxygenase-1 (Hmox1) and lipocalin-2 (Lcn2). Both the anaemia and the mRNA expression changes of iron-related genes were largely absent in C.D2 mice which bear a functional allele of the Nramp1 gene. Data presented in this work suggest that anaemia due to a chronic mycobacterial infection may develop in the absence of elevated hepcidin expression, is influenced by Nramp1 and may involve lipocalin-2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia / metabolism*
  • Anemia / microbiology*
  • Anemia / pathology
  • Animals
  • Antimicrobial Cationic Peptides / genetics
  • Antimicrobial Cationic Peptides / metabolism*
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism*
  • Disease Models, Animal
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Hepcidins
  • Iron / metabolism
  • Lipocalins / genetics
  • Lipocalins / metabolism*
  • Liver / metabolism
  • Liver / pathology
  • Metabolic Networks and Pathways / genetics
  • Mice
  • Mice, Inbred BALB C
  • Mycobacterium avium / physiology*
  • RNA, Messenger / genetics
  • Tuberculosis / metabolism*
  • Tuberculosis / microbiology
  • Tuberculosis / pathology

Substances

  • Antimicrobial Cationic Peptides
  • Cation Transport Proteins
  • Hamp protein, mouse
  • Hepcidins
  • Lipocalins
  • RNA, Messenger
  • natural resistance-associated macrophage protein 1
  • Iron