Ets-1 Maintains IL-7 Receptor Expression in Peripheral T Cells
Author(s) -
Roland Grenningloh,
Tzong-Shyuan Tai,
Nicole Frahm,
Tomoyuki C. Hongo,
Adam Chicoine,
Christian Brander,
Daniel E. Kaufmann,
ICheng Ho
Publication year - 2010
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1002099
Subject(s) - interleukin 7 receptor , biology , cd8 , cytotoxic t cell , microbiology and biotechnology , transcription factor , effector , t cell , il 2 receptor , immune system , immunology , genetics , gene , in vitro
The expression of CD127, the IL-7-binding subunit of the IL-7 R, is tightly regulated during the development and activation of T cells and is reduced during chronic viral infection. However, the molecular mechanism regulating the dynamic expression of CD127 is still poorly understood. In this study, we report that the transcription factor Ets-1 is required for maintaining the expression of CD127 in murine peripheral T cells. Ets-1 binds to and activates the CD127 promoter, and its absence leads to reduced CD127 expression, attenuated IL-7 signaling, and impaired IL-7-dependent homeostatic proliferation of T cells. The expression of CD127 and Ets-1 is strongly correlated in human T cells. Both CD127 and Ets-1 expression are decreased in CD8(+) T cells during HIV infection. In addition, HIV-associated loss of CD127 is only observed in Ets-1(low) effector memory and central memory but not in Ets-1(high) naive CD8(+) T cells. Taken together, our data identify Ets-1 as a critical regulator of CD127 expression in T cells.
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