Th2 Lymphoproliferative Disorders Resulting from Defective LAT Signalosomes

Abstract

LAT (linker for activation of T cells) is an integral membrane adaptor protein that constitutes in T cells a major substrate of the ZAP-70 protein tyrosine kinase. LAT coordinates the assembly of a multiprotein signalling complex through phosphotyrosine-based motifs present within its intracytoplasmic segment. The resulting 'LAT signalosome' links the TCR to the main intracellular signalling pathways that regulate T cell development and T cell function. Early studies using transformed T cell lines suggested that LAT acts primarily as a positive regulator of T cell receptor (TCR) signalling. The partial or complete inhibition of T cell development observed in several mouse lines harbouring mutant forms of LAT was congruent with that view. More recently, LAT 'knock-ins' harbouring point mutations in the four COOH-terminal tyrosine residues, were found to develop lymphoproliferative disorders involving polyclonal T cells that produced high amounts of T helper-type 2 (Th2) cytokines. This unexpected finding revealed that LAT also constitutes a negative regulator of TCR signalling and T cell homeostasis. As discussed, the available data underscore that a novel immunopathology proper to defective LAT signalosome is likely taking shape.