Control of Effector CD8 + T Cell Function by the Transcription Factor Eomesodermin
Mount Sinai Hospital · HistoGenetics (United States) · +1 more institution
Abstract
Activated CD8+ T cells play a critical role in host defense against viruses, intracellular microbes, and tumors. It is not clear if a key regulatory transcription factor unites the effector functions of CD8+ T cells. We now show that Eomesodermin (Eomes), a paralogue of T-bet, is induced in effector CD8+ T cells in vitro and in vivo. Ectopic expression of Eomes was sufficient to invoke attributes of effector CD8+ T cells, including interferon-gamma (IFN-gamma), perforin, and granzyme B. Loss-of-function analysis suggests Eomes may also be necessary for full effector differentiation of CD8+ T cells. We suggest that Eomesodermin is likely to complement the actions of T-bet and act as a key regulatory gene in the…
Citation impact
- FWCI
- 8.02
- Percentile
- 100%
- References
- 18
Authors
17- ELErika L. Pearce
Mount Sinai Hospital, HistoGenetics (United States), University of Pennsylvania
- ACAlan C. Mullen
Mount Sinai Hospital, HistoGenetics (United States), University of Pennsylvania
- GAGislâine A. Martins
Mount Sinai Hospital, HistoGenetics (United States), University of Pennsylvania
- CMConnie M. Krawczyk
Mount Sinai Hospital, HistoGenetics (United States), University of Pennsylvania
- ASAnne S. Hutchins
Mount Sinai Hospital, HistoGenetics (United States), University of Pennsylvania
Topics & keywords
- Effector
- Cell biology
- CD8
- Biology
- Granzyme
- Cytotoxic T cell
- Granzyme B
- Perforin