Posttranscriptional regulation of IL-10 gene expression through sequences in the 3 '-untranslated region

IL-10 is an 18-kDa immunoregulatory cytokine the transcription of which is controlled by the ubiquitously expressed transcription factors Sp1 and Sp3, Although many cell types express IL-10 mRNA, not all make detectable amoun ts of protein, and levels of protein expression vary enormously. We show he re that much of this variation can be accounted for by posttranscriptional mechanisms. Multiple copies of potential mRNA destabilizing motifs AUUUA an d related sequences can be found to the 3'-untranslated region (UTR) of IL- 10 mRNA distributed through three potential regulatory regions. Evidence of RNA-destabilizing activities in all three regions was deduced from lucifer ase reporter assays. The half-life of RNA containing the 3'-UTR of IL-10 mR NA was quite short in both nonstimulated (t(1/2) = 1 h), and PMA-stimulated EL-4 cell (t(1/2) = 3 h). Ill contrast, the half-life of RNA lacking the 3 '-UTR was much longer (t(1/2) = >12 h) whether cells were stimulated or not . This suggests that many cells are poised to secrete IL-10 and will do so if they receive appropriate posttranscriptional signals.