CRIg: A Macrophage Complement Receptor Required for Phagocytosis of Circulating Pathogens

Cell. 2006 Mar 10;124(5):915-27. doi: 10.1016/j.cell.2005.12.039.

Abstract

The complement system serves an important role in clearance of pathogens, immune complexes, and apoptotic cells present in the circulation. Complement fragments deposited on the particle surface serve as targets for complement receptors present on phagocytic cells. Although Kupffer cells, the liver resident macrophages, play a dominant role in clearing particles in circulation, complement receptors involved in this process have yet to be identified. Here we report the identification and characterization of a Complement Receptor of the Immunoglobulin superfamily, CRIg, that binds complement fragments C3b and iC3b. CRIg expression on Kupffer cells is required for efficient binding and phagocytosis of complement C3-opsonized particles. In turn, Kupffer cells from CRIg-deficient mice are unable to efficiently clear C3-opsonized pathogens in the circulation, resulting in increased infection and mortality of the host. CRIg therefore represents a dominant component of the phagocytic system responsible for rapid clearance of C3-opsonized particles from the circulation.

MeSH terms

  • Animals
  • Complement C3 / immunology
  • Complement C3b / immunology
  • Endosomes / metabolism
  • Humans
  • Kupffer Cells / cytology
  • Kupffer Cells / immunology
  • Listeriosis / immunology
  • Macrophages / cytology
  • Macrophages / immunology*
  • Mice
  • Opsonin Proteins / metabolism
  • Peptide Fragments / immunology
  • Phagocytosis / physiology*
  • Protein Binding
  • Receptors, Complement / genetics
  • Receptors, Complement / immunology*
  • Receptors, Complement 3b

Substances

  • CR1 protein, human
  • CRIg protein, mouse
  • Complement C3
  • Opsonin Proteins
  • Peptide Fragments
  • Receptors, Complement
  • Receptors, Complement 3b
  • Complement C3b