Normal T cell homeostasis: the conversion of naive cells into memory-phenotype cells
Weak T cell antigen receptor (TCR) signals from contact with self ligands act in synergy with antiapoptotic signals induced by interleukin 7 (IL-7) to promote the survival of naive T cells in a resting state. The amount of background TCR signaling in naive T cells is set by post-thymic TCR tuning and operates at an intensity just below that required to induce entry into the cell cycle. Costimulation from higher concentrations of IL-7 and other common gamma-chain cytokines can induce T cells to undergo homeostatic proliferation and conversion into cells with a memory phenotype; many of these memory phenotype cells may be the progeny of cells responding to self antigens. The molecular mechanisms that control the conversion of naive resting T cells into memory-phenotype cells TCR-dependent in normal animals are beginning to be understood.
|Authors||Sprent, J.; Surh, C. D.|
|Publisher Name||NAT IMMUNOL|
|Published Date||2011-05-05 00:00:00|
|OpenAccess Link||https://publications.gimr.garvan.org.au/download.php?10954_11427/11 Sprent NI_.pdf|