| First Author | Schmidt AM | Year | 2013 |
| Journal | Sci Signal | Volume | 6 |
| Issue | 303 | Pages | ra101 |
| PubMed ID | 24280042 | Mgi Jnum | J:259526 |
| Mgi Id | MGI:6141935 | Doi | 10.1126/scisignal.2004411 |
| Citation | Schmidt AM, et al. (2013) Diacylglycerol kinase zeta limits the generation of natural regulatory T cells. Sci Signal 6(303):ra101 |
| abstractText | Natural regulatory T (nT(reg)) cells are important for maintaining tolerance to self- and foreign antigens, and they are thought to develop from thymocytes that receive strong T cell receptor (TCR)-mediated signals in the thymus. TCR engagement leads to the activation of phospholipase C-gamma1, which generates the lipid second messenger diacylglycerol (DAG) from phosphatidylinositol 4,5-bisphosphate. We used mice that lack the zeta isoform of DAG kinase (DGKzeta), which metabolizes DAG to terminate its signaling, to enhance TCR-mediated signaling and identify critical signaling events in nT(reg) cell development. Loss of DGKzeta resulted in increased numbers of thymic CD25(+)Foxp3(-)CD4(+) nT(reg) cell precursors and Foxp3(+)CD4(+) nT(reg) cells in a cell-autonomous manner. DGKzeta-deficient T cells exhibited increased nuclear translocation of the nuclear factor kappaB subunit c-Rel, as well as enhanced extracellular signal-regulated kinase (ERK) phosphorylation in response to TCR stimulation, suggesting that these downstream pathways may contribute to nT(reg) cell development. Indeed, reducing c-Rel abundance or blocking ERK phosphorylation abrogated the increased generation of nTreg cells by DGKzeta-deficient thymocytes. The extent of ERK phosphorylation correlated with TCR-mediated acquisition of Foxp3 in immature thymocytes in vitro. Furthermore, the development of nT(reg) cells was augmented in mice in which ERK activation was selectively enhanced in T cells. Together, these data suggest that DGKzeta regulates the development of nT(reg) cells by limiting the extent of activation of the ERK and c-Rel signaling pathways. |
