CD5-mediated negative regulation of antigen receptor-induced growth signals in B-1 B cells

A subset of B lymphocytes present primarily in the peritoneal and pleural cavities is defined by the expression of GD5 and is elevated in autoimmune diseases. Upon signaling through membrane immunoglobulin M (mIgM), splenic B lymphocytes (B-2) proliferate, whereas peritoneal B cells (B-1) undergo apoptosis, However, in CD5-deficient mice, B-1 cells responded to mlgM crosslinking by developing a resistance to apoptosis and entering the cell cycle, In wild-type B-1 cells, prevention of association between CD5 and mlgM rescued their growth response to mlgM crosslinking, Thus the B cell receptor-mediated signaling is negatively regulated by CD5 in normal B-1 cells.