The
Tec (tyrosine kinase expressed in
hepatocellular carcinoma) family of non-
receptor tyrosine kinases consists of five members: Tec,
Bruton's tyrosine kinase (Btk),
inducible T-cell kinase (Itk), resting lymphocyte
kinase (Rlk/Txk), and bone marrow-expressed
kinase (Bmx/Etk). Although their functions are probably best understood in
antigen receptor signaling, where they participate in the phosphorylation and regulation of
phospholipase C-gamma (
PLC-gamma), it is now appreciated that these
kinases contribute to signaling from many receptors and that they participate in multiple downstream pathways, including regulation of the actin cytoskeleton. In T cells, three Tec
kinases are expressed, Itk, Rlk/Txk, and Tec. Itk is expressed at highest amounts and plays the major role in regulating signaling from the
T-cell receptor. Recent studies provide evidence that these
kinases contribute to multiple aspects of T-cell biology and have unique roles in T-cell development that have revealed new insight into the regulation of conventional and innate T-cell development. We review new findings on the Tec
kinases with a focus on their roles in T-cell development and mature T-cell differentiation.