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10.4049/jimmunol.181.11.7902

http://scihub22266oqcxt.onion/10.4049/jimmunol.181.11.7902
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19017980!ä!19017980

suck abstract from ncbi


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pmid19017980      J+Immunol 2008 ; 181 (11): 7902-8
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  • Complement receptor of the Ig superfamily enhances complement-mediated phagocytosis in a subpopulation of tissue resident macrophages #MMPMID19017980
  • Gorgani NN; He JQ; Katschke KJ Jr; Helmy KY; Xi H; Steffek M; Hass PE; van Lookeren Campagne M
  • J Immunol 2008[Dec]; 181 (11): 7902-8 PMID19017980show ga
  • An important function of the complement cascade is to coat self and foreign particles with C3-proteins that serve as ligands for phagocytic receptors. Although tissue resident macrophages play an important role in complement-mediated clearance, the receptors coordinating this process have not been well characterized. In the present study, we identified a subpopulation of resident peritoneal macrophages characterized by high expression of complement receptor of the Ig superfamily (CRIg), a recently discovered complement C3 receptor. Macrophages expressing CRIg showed significantly increased binding and subsequent internalization of complement-opsonized particles compared with CRIg negative macrophages. CRIg internalized monovalent ligands and was able to bind complement-opsonized targets in the absence of Ca(2+) and Mg(2+), which differs from the beta(2)-integrin CR3 that requires divalent cations and polyvalent ligands for activation of the receptor. Although CRIg dominated in immediate binding of complement-coated particles, CRIg and CR3 contributed independently to subsequent particle phagocytosis. CRIg thus identifies a subset of tissue resident macrophages capable of increased phagocytosis of complement C3-coated particles, a function critical for immune clearance.
  • |Animals[MESH]
  • |CD18 Antigens/immunology[MESH]
  • |Calcium/immunology[MESH]
  • |Complement C3/*immunology[MESH]
  • |Gene Expression Regulation/immunology[MESH]
  • |Ligands[MESH]
  • |Macrophages/*immunology[MESH]
  • |Magnesium/immunology[MESH]
  • |Mice[MESH]
  • |Mice, Inbred AKR[MESH]
  • |Mice, Knockout[MESH]
  • |Phagocytosis/*immunology[MESH]


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