Abstract
Modifying the chromatin structure and interacting with non-histone proteins, histone deacetylases (HDAC) are involved in vital cellular processes at different levels. We here specifically investigated the direct effects of HDAC5 in macrophage activation in response to bacterial or cytokine stimuli. Using murine and human macrophage cell lines, we studied the expression profile and the immunological function of HDAC5 at transcription and protein level in over-expression as well as RNA interference experiments. Toll-like receptor-mediated stimulation of murine RAW264.7 cells significantly reduced HDAC5 mRNA within 7 hrs but presented baseline levels after 24 hrs, a mechanism that was also found for Interferon-γ treatment. If treated with lipopolysaccharide, RAW264.7 cells transfected for over-expression only of full-length but not of mutant HDAC5, significantly elevated secretion of tumour necrosis factor α and of the monocyte chemotactic protein-1. These effects were accompanied by increased nuclear factor-κB activity. Accordingly, knock down of HDAC5-mRNA expression using specific siRNA significantly reduced the production of these cytokines in RAW264.7 or human U937 cells. Taken together, our results suggest a strong regulatory function of HDAC5 in the pro-inflammatory response of macrophages.
Highlights
Gene transcription is regulated by multiple mechanisms including modifications of the DNA itself or of changes in DNA-associated histones
The presence of HDAC5 built the prerequisite for all experiments and so we assessed the baseline expression of the enzyme in murine RAW264.7 and human U937 cells
As the question was whether pro-inflammatory activation influenced HDAC5 expression levels, RAW264.7 cells were stimulated with LPS
Summary
Gene transcription is regulated by multiple mechanisms including modifications of the DNA itself or of changes in DNA-associated histones. Making use of murine and human macrophage cell lines, we studied the effect of HDAC5 over-expression and knock-down on nuclear factor kappa B (NF-jB)-dependent regulation of cytokine and chemokine expression. To assess the milieu dependent expression of HDAC5 mRNA, RAW264.7 cells were subjected to defined chemotaxis-inducing, anti-inflammatory, polarizing or pro-inflammatory conditions for 5 to 7 hrs.
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