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Publication : Antigen receptor editing in anti-DNA transitional B cells deficient for surface IgM.

First Author  Kiefer K Year  2008
Journal  J Immunol Volume  180
Issue  9 Pages  6094-106
PubMed ID  18424731 Mgi Jnum  J:160356
Mgi Id  MGI:4454309 Doi  10.4049/jimmunol.180.9.6094
Citation  Kiefer K, et al. (2008) Antigen receptor editing in anti-DNA transitional B cells deficient for surface IgM. J Immunol 180(9):6094-106
abstractText  In response to encounter with self-Ag, autoreactive B cells may undergo secondary L chain gene rearrangement (receptor editing) and change the specificity of their Ag receptor. Knowing at what differentiative stage(s) developing B cells undergo receptor editing is important for understanding how self-reactive B cells are regulated. In this study, in mice with Ig transgenes coding for anti-self (DNA) Ab, we report dsDNA breaks indicative of ongoing secondary L chain rearrangement not only in bone marrow cells with a pre-B/B cell phenotype but also in immature/transitional splenic B cells with little or no surface IgM (sIgM(-/low)). L chain-edited transgenic B cells were detectable in spleen but not bone marrow and were still found to produce Ab specific for DNA (and apoptotic cells), albeit with lower affinity for DNA than the unedited transgenic Ab. We conclude that L chain editing in anti-DNA-transgenic B cells is not only ongoing in bone marrow but also in spleen. Indeed, transfer of sIgM(-/low) anti-DNA splenic B cells into SCID mice resulted in the appearance of a L chain editor (Vlambdax) in the serum of engrafted recipients. Finally, we also report evidence for ongoing L chain editing in sIgM(low) transitional splenic B cells of wild-type mice.
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