A Transcriptional Block in the IL-2 Promoter at the −150 AP-1 Site in Effector CD8+ T Cells

Abstract

Both CD4+ and CD8+ T cells that produce IL-2 in response to Ag recognition have been isolated. However, most effector CD8+ T cells recovered after exposure to Ag do not produce sufficient IL-2 to sustain growth, and depend on CD4+ T helper cells for this obligate growth factor. IL-2 expression in CD4+ T cells is primarily controlled at the level of transcription, but mechanisms restricting IL-2 production in CD8+ T cells have not been elucidated. To evaluate transcriptional regulation of the IL-2 gene in CD8+ T cells, we stably transfected reporter genes into Ag-specific CD8+ T cell clones. CD28+ CD8+ T cells unable to transcribe the IL-2 gene in response to antigenic stimulation had a block in transactivation of the −150 CD28 response element (CD28RE)/AP-1 site of the IL-2 promoter, but did transactivate the composite NFAT/AP-1 and OCT/AP-1 sites, and a consensus AP-1 motif. Mutation of the nonconsensus −150 AP-1 site to a consensus AP-1 site, or insertion of a CD28RE/AP-1 consensus site upstream of the native −150 CD28RE/AP-1 site restored transactivation of the altered promoter. These results suggest that the defect at the −150 site may reflect the absence or inactivity of a required factor rather than repression of the IL-2 promoter.