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Expression of the Leukocyte Early Activation Antigen CD69 Is Regulated by the Transcription Factor AP-1

Abstract:

The leukocyte Ag CD69, one of the earliest cell surface activation Ags, is up-regulated at the transcriptional level by proinflammatory stimuli involving the NF-κB/Rel family of transcription factors. However, promoter fragments lacking a critical κB motif respond to other stimuli such as phorbol esters and triggering Abs against TCR/CD3. Since the 5′ promoter flanking region of the CD69 gene contains several putative binding sequences for transcription factor activating protein-1 (AP-1), we explored its role in the inducible expression of CD69. Stimuli that induce AP-1, but not NF-κB, such as pyrrolidine dithiocarbamate, augmented the cell surface expression of CD69 as well as its mRNA levels, and the promoter activity of the CD69 gene. This up-regulation is accompanied by an increased binding of jun and fos family members to a consensus AP-1 binding site of the proximal (-16) CD69 promoter region, which seems to be functionally responsive to different activation signals and is trans-activated by c-jun expression vectors. Furthermore, cotransfection of a dominant negative version of c-jun, but not IκB, abolished the inducible transcriptional activity of the CD69 promoter. In conclusion, the inducible expression of the CD69 gene by mitogenic signals is regulated by the transcription factor AP-1.