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Co‐operation between human CR1 (CD35) and CR2 (CD21) in internalization of their C3b and iC3b ligands by murine‐transfected fibroblasts
Author(s) -
Grattone Ml,
Villiers Cl,
MarieBernadette Villiers,
Christian Drouet,
Patrice N. Marche
Publication year - 1999
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1046/j.1365-2567.1999.00839.x
Subject(s) - ic3b , internalization , transfection , receptor , microbiology and biotechnology , immunoprecipitation , chemistry , hek 293 cells , antibody , biology , monoclonal antibody , immunology , gene , biochemistry
CR1 and CR2 are expressed as associated proteins on the B‐lymphocyte surface. To investigate their respective contributions to the internalization of C3 fragments, transfected murine fibroblasts expressing human CR1, CR2, or both CR1 and CR2 were produced. CR1‐ and CR1–CR2‐expressing cells bound C3b and C3b‐dimer whereas CR2‐ and CR1–CR2‐expressing cells bound iC3b and C3de. In all cases, maximum binding was achieved at low ionic strength. CR1–CR2‐positive cells internalized two‐ to threefold more C3b and 1·5‐fold more iC3b than CR1‐ and CR2‐single‐positive cells, respectively. Internalization of the anti‐CR1 antibody J3D3, or C3de was at the same level, in both double‐transfected and single‐transfected cells. Furthermore, the internalization of C3b dimer by CR1–CR2 cells was impaired in the presence of OKB7, an anti‐CR2‐blocking antibody, but it was not altered in CR1 cells. Taken together, these findings suggest that CR1 and CR2 collaborate to internalize C3b and iC3b proteins. We suggest that the induction of conformational changes of the ligands enhances their binding to both receptors.