Linked Life Data

15585857

Source:http://linkedlifedata.com/resource/pubmed/id/15585857

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pubmed-article:15585857pubmed:abstractTextAg-specific immune tolerance results from the induction of cellular mechanisms that limit T cell responses to selective Ags. One of these mechanisms is characterized by attenuated proliferation and decreased IL-2 production in fully stimulated CD4(+) Th cells and is denoted T cell anergy. We report the identification of the early growth response gene (Egr-2; Krox-20), a zinc-finger transcription factor, as a key protein required for induction of anergy in cultured T cells. Gene array screening revealed high Egr-2 expression distinctly persists in anergized but not proliferating murine A.E7 T cells. In contrast, Egr-1, a related family member induced upon costimulation, displays little or no expression in the anergic state. IL-2-mediated abrogation of anergy causes rapid depletion of Egr-2 protein. Full stimulation of anergic A.E7 T cells fails to enhance IL-2 and Egr-1 expression, whereas Egr-2 expression is greatly increased. Silencing Egr-2 gene expression by small interfering RNA treatment of cultured A.E7 T cells before incubation with anti-CD3 alone prevents full induction of anergy. However, small interfering RNA-mediated depletion of Egr-2 5 days after anergy induction does not appear to abrogate hyporesponsiveness to stimulation. These data indicate that sustained Egr-2 expression is necessary to induce a full anergic state through the actions of genes regulated by this transcription factor.lld:pubmed
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pubmed-article:15585857pubmed:articleTitleEarly growth response gene-2, a zinc-finger transcription factor, is required for full induction of clonal anergy in CD4+ T cells.lld:pubmed
pubmed-article:15585857pubmed:affiliationProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655, USA.lld:pubmed
pubmed-article:15585857pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15585857pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:15585857pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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