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10.1016/j.jaut.2014.03.004

http://scihub22266oqcxt.onion/10.1016/j.jaut.2014.03.004
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suck abstract from ncbi


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pmid24768065
      J+Autoimmun 2014 ; 53 (ä): 78-84
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  • The Mertk receptor tyrosine kinase promotes T-B interaction stimulated by IgD B-cell receptor cross-linking #MMPMID24768065
  • Shao WH ; Zhen Y ; Finkelman FD ; Cohen PL
  • J Autoimmun 2014[Sep]; 53 (ä): 78-84 PMID24768065 show ga
  • The Mertk receptor tyrosine kinase facilitates macrophage and DC apoptotic-cell clearance and regulates immune tolerance. Mertk may also contribute to B-cell activation, because Mertk-KO mice fail to develop autoantibodies when allo-activated by T cells. We investigated this possibility with a well-characterized model in which injection of mice with goat anti-IgD antibody causes membrane IgD cross-linking that induces T-independent B cell activation and antigen presentation to T cells. Goat anti-mouse IgD antibody-injected C57BL/6 Mertk-KO mice had normal initial B cell activation and proliferation, but significantly lower T cell activation and proliferation, as well as lower IgE and IgG anti-goat IgG responses, as compared to C57BL/6 WT controls. B cell antigen processing, analyzed by evaluating B cell fluorescence following injection of monoclonal anti-IgD antibody labeled with biotin or FITC, was comparable between Mertk-KO mice and WT mice. IgD Ab primed B cells from Mertk-KO mice exhibited significantly lower ability in activating memory T cells isolated from WT mice injected with the same antigen 10 days before. These observations suggest that Mertk expression is required for optimal B-cell antigen presentation, which is, in turn, required in this model for optimal T cell activation and subsequent T cell-dependent B cell differentiation.
  • |Animals [MESH]
  • |B-Lymphocytes/cytology/*immunology [MESH]
  • |Cell Communication/genetics/*immunology [MESH]
  • |Cell Differentiation/genetics/immunology [MESH]
  • |Gene Expression Regulation, Enzymologic/genetics/immunology [MESH]
  • |Immunoglobulin D/genetics/*immunology [MESH]
  • |Immunologic Capping/genetics/immunology [MESH]
  • |Immunologic Memory/genetics [MESH]
  • |Lymphocyte Activation/genetics [MESH]
  • |Mice [MESH]
  • |Mice, Knockout [MESH]
  • |Proto-Oncogene Proteins/genetics/*immunology [MESH]
  • |Receptor Protein-Tyrosine Kinases/genetics/*immunology [MESH]
  • |Receptors, Antigen, B-Cell/genetics/*immunology [MESH]
  • |T-Lymphocytes/cytology/*immunology [MESH]


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