Akt Fine-tunes NF-kappa B-dependent Gene Expression during T Cell Activation

作者：Cheng Jing; Phong Binh; Wilson David C; Hirsch Raphael; Kane Lawrence P^*

来源：Journal of Biological Chemistry, 2011, 286(41): 36076-36085.

DOI：10.1074/jbc.M111.259549

Activation of the NF-kappa B signaling pathway is critical for leukocyte activation and development. Although previous studies suggested a role for the Akt kinase in coupling the T cell antigen receptor and CD28 to NF-kappa B activation in T cells, the nature of the role of Akt in this pathway is still unclear. Using a targeted gene profiling approach, we found that a subset of NF-kappa B-dependent genes required Akt for optimal up-regulation during T cell activation. The selective effects of Akt were manifest at the level of mRNA transcription and p65/RelA binding to upstream promoters and appear to be due to altered formation of the Carma1-Bcl10 complex. The proinflammatory cytokine TNF-alpha was found to be particularly sensitive to Akt inhibition or knockdown, including in primary human blood T cells and a murine model of rheumatoid arthritis. Our findings are consistent with a hierarchy in the expression of NF-kappa B-dependent genes, controlled by the strength and/or duration of NF-kappa B signaling. More broadly, our results suggest that defining the more graded effects of signaling, such as those demonstrated here for Akt and the NF-kappa B pathway, is important to understanding how cells can fine-tune signaling responses for optimal sensitivity and specificity.

• 出版日期2011-10-14