Engagement of MHC class II and CD40 on B cell lines triggers intracellular
signals that activates cell surface adhesion receptors, resulting in LFA-I-
dependent and -independent cell-cell adhesion. In this study, a murine mono
clonal antibody (mAb R21) has been produced against a LFA-l-negative human
B cell line and proven to completely block MHC class II-and CD40-induced LF
A-I-independent homotypic adhesion. However, this mAb failed to prevent MHC
class II- or CD40-induced homotypic adhesion in LFA-l-positive Raji B cell
s, and alone, it triggered LFA-l-dependent cell-cell adhesion. Biochemical
characterization indicated that the CD20 molecule, a tetraspan phosphoprote
in expressed on B cells that functions as a Ca2+-conductive ion channel, is
the target of mAb R21. Interestingly, further biochemical analysis demonst
rated that CD20 is physically associated with MHC class II and CD40 molecul
es on the cell surface of LFA-l-negative and LFA-l-positive B cell lines. A
lthough these three molecules are associated with each other, the complex f
ormation between any two of them is not dependent on the simultaneous expre
ssion of the three molecules. Altogether, these results indicate that CD20
is physically and probably functionally coupled to the MHC class II and CD4
0 molecules; thereby it may have certain modulatory effects on their functi
ons.