Y. Aoki et al., BRUTON TYROSINE KINASE IS TYROSINE-PHOSPHORYLATED AND ACTIVATED IN PRE-B LYMPHOCYTES AND RECEPTOR-LIGATED B-CELLS, Proceedings of the National Academy of Sciences of the United Statesof America, 91(22), 1994, pp. 10606-10609
The gene encoding Bruton tyrosine kinase (Btk) is known to be mutated
in human X chromosome-linked agammaglobulinemia and in the Xid mouse.
This kinase was examined in B lymphocytes before and after antigen rec
eptor ligation and also in pre-B cells. Btk was found to be catalytica
lly activated and tyrosine phosphorylated in response to anti-IgM stim
ulation in B cells. This kinase is also constitutively phosphorylated
on tyrosine residues in pre-B cells. These findings point to a functio
nal role for Btk in pre-antigen and antigen receptor signaling during
B-cell development and provide a biochemical explanation for the X-lin
ked genetic syndromes already linked to this kinase.