B lymphopoiesis is regulated by multiple signals from stromal cell con
tact, soluble cytokines, antigen, and T helper cells. In vitro and bio
chemical experiments have implicated tyrosine kinases as key component
s of many of these signaling pathways. Genetic analysis of the role of
these tyrosine kinases has been facilitated by recent advances in tra
nsgenic and gene targeting technology as well as by the identification
of the genetic basis of several human and murine immune deficiencies.
This review discusses the effect of gain and loss of function mutatio
ns of selected tyrosine kinases and their regulators and substrates on
B cell development and function.