Abstract
The physiological role of histone deacetylase 11 (HDAC11), the newest member of the HDAC family, remained largely unknown until the discovery of its regulatory function in immune cells. Among them, the regulation of cytokine production by antigen-presenting cells and the modulation of the suppressive ability of myeloid-derived suppressor cells (MDSCs) (Sahakian et al. Mol Immunol 63: 579–585, 2015; Wang et al. J Immunol 186: 3986–3996, 2011; Villagra et al. Nat Immunol 10: 92–100, 2009). Our earlier data has demonstrated that HDAC11, by interacting at the chromatin level with the IL-10 promoter, downregulates il-10 transcription in both murine and human APCs in vitro and ex vivo models (Villagra et al. Nat Immunol 10: 92–100, 2009). However the role of HDAC11 in other cell types still remains unknown. Here we present several methods that can potentially be used to identify the functional role of HDAC11, assigning special attention to the evaluation of immunological parameters.
The original version of this chapter was revised. The erratum to this chapter is available at: DOI 10.1007/978-1-4939-3667-0_22
An erratum to this chapter can be found at http://dx.doi.org/10.1007/978-1-4939-3667-0_22
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Acknowledgments
The authors gratefully acknowledge the flow cytometry core facilities at H. Lee Moffitt Cancer Center and their extended technical support for our project.
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Chen, J. et al. (2016). Functional Analysis of Histone Deacetylase 11 (HDAC11). In: Sarkar, S. (eds) Histone Deacetylases. Methods in Molecular Biology, vol 1436. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-3667-0_11
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DOI: https://doi.org/10.1007/978-1-4939-3667-0_11
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