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Inflammation Research

, Volume 47, Issue 7, pp 277–284 | Cite as

Macrophage NRAMP1 and its role in resistance to microbial infections

  • G. Govoni
  • P. Gros

Abstract.

The identification and characterization of genetic factors influencing natural susceptibility to infectious diseases in humans and in model organisms, such as the laboratory mouse, can provide new insight into the basic mechanisms of host defense against infections. In the mouse, resistance or susceptibility to infection with intracellular pathogens such as Salmonella, Mycobacterium and Leishmania is controlled by the Natural resistance associated macrophage protein (Nramp1) gene on chromosome 1, which influences the rate of intracellular replication of these parasites in macrophages. Nramp1 codes for an integral membrane protein, which is expressed exclusively in macrophage/monocytes and polymorphonuclear leukocytes. The protein is localized to the endosomal/lysosomal compartment of the macrophage and is rapidly recruited to the membrane of the particle-containing phagosome upon phagocytosis. Nramp defines a novel family of functionally related membrane proteins including Nramp2, which was recently shown to be the major transferrin-independent uptake system of the intestine in mammals. This observation supports the hypothesis that the phagocyte-specific Nramp1 protein may regulate the intraphagosomal replication of antigenically unrelated bacteria by controlling divalent cation concentrations at that site. Recent genetic studies have found that allelic variants at the human NRAMP1 locus are associated with susceptibility to leprosy (Mycobacterium leprae) and tuberculosis (Mycobacterium tuberculosis) and possibly with the onset of rheumatoid arthritis.

Key words: Mononuclear phagocytes — Infectious diseases — Divalent cations transport — Intracellular parasites 

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Copyright information

© Birkhäuser Verlag, Basel, 1998

Authors and Affiliations

  • G. Govoni
    • 1
  • P. Gros
    • 1
  1. 1.Department of Biochemistry, McGill University, Montreal, Quebec H3G 1Y6, Canada, e-mail: gros@medcor.mcgill.caCA

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