ZAP70 tyrosine kinase plays an essential role in the regulation of the adaptive immune response. It regulates motility, adhesion and cytokine expression of mature T cells as well as thymocyte development. Furthermore, it also contributes to the development and activation of primary B lymphocytes (Fischer A et al. 2010).
When antigen-presenting cells (APC) activate the T cell receptor (TCR), phosphorylation leads to the recruitment of ZAP70 to the TCR component CD247/CD3Z via the ITAM motif at the plasma membrane. Subsequently, ZAP70 phosphorylates at least 2 key adapter proteins: LAT and LCP2. In turn, it recruits a large number of signaling molecules that ultimately lead to lymphokine production, T cell proliferation and differentiation.
In addition, ZAP70 controls cytoskeletal modifications, adhesion, and mobility of T lymphocytes, ensuring proper delivery of effectors to the APC.
ZAP70 further regulates both on and off T cell activation by modulating TCR expression at the T cell surface.
During thymocyte development, ZAP70 promotes survival and cell cycle progression of developing thymocytes prior to positive selection (when cells are still CD4/CD8 double negative).
Furthermore, the ZAP70-dependent signaling pathway may also contribute to the formation and activation of primary B cells through the B cell receptor (BCR).