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Local BLyS production by T follicular cells mediates retention of high affinity B cells during affinity maturation.

The Journal of experimental medicine (2013-12-25)
Radhika Goenka, Andrew H Matthews, Bochao Zhang, Patrick J O'Neill, Jean L Scholz, Thi-Sau Migone, Warren J Leonard, William Stohl, Uri Hershberg, Michael P Cancro
RESUMEN

We have assessed the role of B lymphocyte stimulator (BLyS) and its receptors in the germinal center (GC) reaction and affinity maturation. Despite ample BLyS retention on B cells in follicular (FO) regions, the GC microenvironment lacks substantial BLyS. This reflects IL-21-mediated down-regulation of the BLyS receptor TACI (transmembrane activator and calcium modulator and cyclophilin ligand interactor) on GC B cells, thus limiting their capacity for BLyS binding and retention. Within the GC, FO helper T cells (TFH cells) provide a local source of BLyS. Whereas T cell-derived BLyS is dispensable for normal GC cellularity and somatic hypermutation, it is required for the efficient selection of high affinity GC B cell clones. These findings suggest that during affinity maturation, high affinity clones rely on TFH-derived BLyS for their persistence.

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GenElute HP Plasmid Miniprep Kit, sufficient for 350 preparations
Sigma-Aldrich
GenElute HP Plasmid Miniprep Kit, sufficient for 70 preparations