| Literature DB >> 24747960 |
Fengdong Cheng1, Maritza Lienlaf1, Patricio Perez-Villarroel1, Hong-Wei Wang1, Calvin Lee2,3, Karrune Woan1, David Woods1, Tessa Knox1, Joel Bergman4, Javier Pinilla-Ibarz1, Alan Kozikowski4, Edward Seto5, Eduardo M Sotomayor1, Alejandro Villagra1.
Abstract
The anti-inflammatory cytokine IL-10 is a key modulator of immune responses. A better understanding of the regulation of this cytokine offers the possibility of tipping the balance of the immune response toward either tolerance, or enhanced immune responses. Histone deacetylases (HDACs) have been widely described as negative regulators of transcriptional regulation, and in this context, the primarily nuclear protein HDAC11 was shown to repress il-10 gene transcriptional activity in antigen-presenting cells (APCs). Here we report that another HDAC, HDAC6, primarily a cytoplasmic protein, associates with HDAC11 and modulates the expression of IL-10 as a transcriptional activator. To our knowledge, this is the first demonstration of two different HDACs being recruited to the same gene promoter to dictate divergent transcriptional responses. This dynamic interaction results in dynamic changes in the expression of IL-10 and might help to explain the intrinsic plasticity of the APC to determine T-cell activation versus T-cell tolerance.Entities:
Keywords: Antigen presenting cells; HDAC11; HDAC6; IL-10; Tolerance
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Year: 2014 PMID: 24747960 PMCID: PMC4020151 DOI: 10.1016/j.molimm.2014.02.019
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407