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Publication : Id2-mediated inhibition of E2A represses memory CD8+ T cell differentiation.

First Author  Masson F Year  2013
Journal  J Immunol Volume  190
Issue  9 Pages  4585-94
PubMed ID  23536629 Mgi Jnum  J:195516
Mgi Id  MGI:5484709 Doi  10.4049/jimmunol.1300099
Citation  Masson F, et al. (2013) Id2-Mediated Inhibition of E2A Represses Memory CD8+ T Cell Differentiation. J Immunol 190(9):4585-94
abstractText  The transcription factor inhibitor of DNA binding (Id)2 modulates T cell fate decisions, but the molecular mechanism underpinning this regulation is unclear. In this study we show that loss of Id2 cripples effector differentiation and instead programs CD8(+) T cells to adopt a memory fate with increased Eomesodermin and Tcf7 expression. We demonstrate that Id2 restrains CD8(+) T cell memory differentiation by inhibiting E2A-mediated direct activation of Tcf7 and that Id2 expression level mirrors T cell memory recall capacity. As a result of the defective effector differentiation, Id2-deficient CD8(+) T cells fail to induce sufficient Tbx21 expression to generate short-lived effector CD8(+) T cells. Our findings reveal that the Id2/E2A axis orchestrates T cell differentiation through the induction or repression of downstream transcription factors essential for effector and memory T cell differentiation.
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