Importantly, reconstitution of FcγRIIB−/− mice with FcγRIIB+ B cells confers protection from disease, as does increasing the level of FcγRIIB expression through retroviral transduction 8. Together, these data suggest that B-cell expression of FcγRIIB is essential for the maintenance B-cell peripheral tolerance. see more Early studies demonstrated that immune complexes (IC), composed

of rabbit F(ab′)2 anti-IgM bound by mouse IgG, activated B cells significantly less well than F(ab′)2 anti-IgM alone 9. However, chromatin/DNA-associated IC, present in the sera of autoimmune mice, very effectively activate both IgG2a-reactive high-affinity 20.8.3 and low-affinity AM14 B cells 10, 11. AM14 B-cell activation required engagement of both the BCR and TLR9 12. TLR9 was originally described as a pattern recognition receptor specific for particular DNA sequences, Silmitasertib cell line designated CpG motifs, frequently found in bacterial but not mammalian DNA 13. Nevertheless, the role of TLR9 in the detection of DNA-associated IC, as described above, clearly demonstrated that TLR9 also detects mammalian DNA. To better understand the nature of the endogenous TLR9 ligand, we have constructed dsDNA fragment IC that incorporate biotinylated DNA fragments bound by an IgG2a anti-biotin mAb. Stimulation of AM14 B cells with IC containing dsDNA fragments

corresponding Dolichyl-phosphate-mannose-protein mannosyltransferase to the CG-rich sequences derived from endogenous CpG islands

strongly activate AM14 B-cell proliferation, whereas IC containing dsDNA fragments representative of the overall mammalian genome do not 14. The availability of DNA fragments that can engage TLR9 to varying degrees provides a useful tool for examining the regulation of autoreactive B-cell activation. Like TLR9, TLR7 is also located in endosomal compartments; however, this receptor recognizes single-stranded RNA 15–17. In an analogous manner to the BCR/TLR9 paradigm, RNA IC promote AM14 B-cell responses through a mechanism that involves both the BCR and the TLR7 18. However, AM14 B-cell responses to RNA IC are generally more dependent on coactivation with type I IFN. We had previously shown that FcγRIIB deficiency did not affect the capacity of high-affinity IgG2a-specific B cells to respond to chromatin IC 11. At the time, we surmised that the cell surface expression of FcγRIIB precluded its capacity to regulate signaling cascades emanating from TLR7 and TLR9, which were predominantly found in endosomal compartments. The capacity of FcγRIIB has now been re-examined in the context of low-affinity IgG2a-reactive AM14 B cells activated by chromatin/DNA and RNA IC. We find that FcγRIIB can regulate AM14 IC responses to DNA IC only when the complexes contain CpG-poor DNA. FcγRIIB further modulates AM14 B-cell responses to RNA IC, both in the absence and in the presence of IFN-α.