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10.1093/glycob/cwu068

http://scihub22266oqcxt.onion/10.1093/glycob/cwu068
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C4116048!4116048!24996822
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suck abstract from ncbi


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pmid24996822      Glycobiology 2014 ; 24 (9): 800-6
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  • Siglec-G/10 in self?nonself discrimination of innate and adaptive immunity #MMPMID24996822
  • Chen GY; Brown NK; Zheng P; Liu Y
  • Glycobiology 2014[Sep]; 24 (9): 800-6 PMID24996822show ga
  • Siglec-G/10 is broadly expressed on B cells, dendritic cells and macrophage subsets. It binds strongly to CD24, a small glycosyl-phosphatidylinositol-anchored sialoprotein, in a sialylation-dependent manner. Targeted mutation of Siglecg dramatically elevates the level of natural IgM antibodies and its producer, B1 B cells. Incorporation of Siglec-G ligands to both T-dependent and T-independent immunogens reduces antibody production and induces B-cell tolerance to subsequent antigen challenges. By interacting with CD24, Siglec-G suppresses inflammatory responses to danger (damage)-associated molecular patterns, such as heat-shock proteins and high mobility group protein 1, but not to Toll-like receptor ligands. By a CD24-independent mechanism, Siglec-G has been shown to associate with Cbl to cause degradation of retinoic acid-inducible gene 1 and reduce production of type I interferon in response to RNA virus infection. The negative regulation by Siglec-G/10 may provide a mechanism for the host to discriminate between infectious nonself and noninfectious self, as envisioned by the late Dr. Charles A. Janeway.
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