CD23 is a low-affinity receptor for IgE (Fc epsilon RII). Functions at
tributed to CD23 not involving IgE suggest that it interacts with liga
nds other than IgE. CD21 has recently been described as a counter liga
nd for CD23. A number of lines of evidence have implicated CD23 as an
adhesion molecule in human B cells. We have investigated the role of C
D23 in homotypic B cell aggregation in the mouse, using lipopolysaccha
ride plus interleukin-4-induced aggregation as a model system. In this
system high levels of aggregation are accompanied by a massive up-reg
ulation of CD23 expression. However, in contrast to what has been obse
rved in human B cells, we find no evidence of a role for CD23 in homot
ypic adhesion of murine B cells.