TY - JOUR
T1 - Essential role of the T cell-specifi c adapter protein in the activation of LCK in peripheral T cells
AU - Marti, Francesc
AU - Garcia, Gonzalo G.
AU - Lapinski, Philip E.
AU - MacGregor, Jennifer N.
AU - King, Philip D.
PY - 2006/2/20
Y1 - 2006/2/20
N2 - T cell-specifi c adapter protein (TSAd) is a SRC-homology-2 (SH2) domain-containing intracellular signaling molecule that is required for T cell antigen receptor (TCR)-induced cytokine synthesis in T cells. How TSAd functions in TCR signal transduction is not clear. Previous work has suggested a nuclear role for this adapter. However, other evidence suggests that TSAd also functions in the cytoplasm. Using T cells from TSAd-defi cient mice, we now show that the major role of TSAd in the cytoplasm is in activation of the LCK proteintyrosine kinase at the outset of TCR signal transduction. Consequently, TSAd regulates several downstream signaling events, including intracellular calcium mobilization and activation of the Ras-extracellular signal-regulated kinase signaling pathway. TSAd regulates LCK activity directly through physical interaction with LCK SH3 and SH2 domains. These studies reveal TSAd as a positive regulator of proximal TCR signal transduction and provide important new information on the mechanism of TCR-induced LCK activation.
AB - T cell-specifi c adapter protein (TSAd) is a SRC-homology-2 (SH2) domain-containing intracellular signaling molecule that is required for T cell antigen receptor (TCR)-induced cytokine synthesis in T cells. How TSAd functions in TCR signal transduction is not clear. Previous work has suggested a nuclear role for this adapter. However, other evidence suggests that TSAd also functions in the cytoplasm. Using T cells from TSAd-defi cient mice, we now show that the major role of TSAd in the cytoplasm is in activation of the LCK proteintyrosine kinase at the outset of TCR signal transduction. Consequently, TSAd regulates several downstream signaling events, including intracellular calcium mobilization and activation of the Ras-extracellular signal-regulated kinase signaling pathway. TSAd regulates LCK activity directly through physical interaction with LCK SH3 and SH2 domains. These studies reveal TSAd as a positive regulator of proximal TCR signal transduction and provide important new information on the mechanism of TCR-induced LCK activation.
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U2 - 10.1084/jem.20051637
DO - 10.1084/jem.20051637
M3 - Article
C2 - 16446380
AN - SCOPUS:33645384693
SN - 0022-1007
VL - 203
SP - 281
EP - 287
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 2
ER -