Follicular dendritic cells (FDCs) are potent accessory cells for B cells, b
ut the molecular basis of their activity is not understood. Several importa
nt molecules involved in FDC-B-cell interactions are indicated by blocking
the ligands and receptors on FDCs and/or B cells. The engagement of CD21 in
the B-cell coreceptor complex by complement-derived CD21 ligand on FDCs de
livers a crucial signal that dramatically augments the stimulation delivere
d by the binding of antigen to the B-cell receptor (BCR). The engagement of
Fc gamma receptor IIB (Fc gamma RIIB) by the Ig crystallizable fragment (F
c) in antigen-antibody complexes held on FDCs decreases the activation of i
mmunoreceptor tyrosine-based inhibition motifs (ITIMs), mediated by the cro
sslinking of BCR and Fc gamma RIIB. Thus, FDCs minimize a negative B-cell s
ignal. In short, these ligand-receptor interactions help to signal to B cel
ls and meet a requirement for B-cell stimulation that goes beyond the neces
sity of T-cell help.