TY - JOUR
T1 - Transcriptional complexes formed by NFAT dimers regulate the induction of T cell tolerance
AU - Soto-Nieves, Noemi
AU - Puga, Irene
AU - Abe, Brian T.
AU - Bandyopadhyay, Sanmay
AU - Baine, Ian
AU - Rao, Anjana
AU - Macian, Fernando
PY - 2009/4/13
Y1 - 2009/4/13
N2 - In T cells, anergy can be induced after T cell receptor engagement in the absence of costimulation. Under these conditions, the expression of a specifc set of anergy-associated genes is activated. Several lines of evidence suggest that nuclear factor of activated T cells (NFAT) proteins may regulate the expression of many of those genes; however, the nature of the complexes responsible for the induction of this new program of gene expression is unknown. Here, we show that transcriptional complexes formed by NFAT homodimers are directly responsible for the activation of at least two anergy-inducing genes, Grail and Caspase3. Our data shows that Grail expression is activated by direct binding of NFAT dimers to the Grail promoter at two different sites. Consequently, a mutant NFAT protein with impaired ability to dimerize is not able to induce an unresponsive state in T cells. Our results not only identify a new biological function for NFAT dimers but also reveal the different nature of NFAT-containing complexes that induce anergy versus those that are activated during a productive immune response. These data also establish a basis for the design of immunomodulatory strategies that specifcally target each type of complex.
AB - In T cells, anergy can be induced after T cell receptor engagement in the absence of costimulation. Under these conditions, the expression of a specifc set of anergy-associated genes is activated. Several lines of evidence suggest that nuclear factor of activated T cells (NFAT) proteins may regulate the expression of many of those genes; however, the nature of the complexes responsible for the induction of this new program of gene expression is unknown. Here, we show that transcriptional complexes formed by NFAT homodimers are directly responsible for the activation of at least two anergy-inducing genes, Grail and Caspase3. Our data shows that Grail expression is activated by direct binding of NFAT dimers to the Grail promoter at two different sites. Consequently, a mutant NFAT protein with impaired ability to dimerize is not able to induce an unresponsive state in T cells. Our results not only identify a new biological function for NFAT dimers but also reveal the different nature of NFAT-containing complexes that induce anergy versus those that are activated during a productive immune response. These data also establish a basis for the design of immunomodulatory strategies that specifcally target each type of complex.
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U2 - 10.1084/jem.20082731
DO - 10.1084/jem.20082731
M3 - Article
C2 - 19307325
AN - SCOPUS:65549083493
SN - 0022-1007
VL - 206
SP - 867
EP - 876
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 4
ER -