Please use this identifier to cite or link to this item:http://hdl.handle.net/20.500.12105/7244
HDAC6 controls innate immune and autophagy responses to TLR-mediated signalling by the intracellular bacteria Listeria monocytogenes
Moreno-Gonzalo, Olga CNIC | Ramirez-Huesca, Marta CNIC | Blas-Rus, Noelia CNIC | Cibrián, Danay | Saiz, Maria Laura CNIC | Jorge, Inmaculada CNIC | Camafeita, Emilio CNIC | Vazquez, Jesus CNIC | Sanchez-Madrid, Francisco CNIC
PLoS Pathog. 2017; 13(12):e1006799
Recent evidence on HDAC6 function underlines its role as a key protein in the innate immune response to viral infection. However, whether HDAC6 regulates innate immunity during bacterial infection remains unexplored. To assess the role of HDAC6 in the regulation of defence mechanisms against intracellular bacteria, we used the Listeria monocytogenes (Lm) infection model. Our data show that Hdac6-/- bone marrow-derived dendritic cells (BMDCs) have a higher bacterial load than Hdac6+/+ cells, correlating with weaker induction of IFN-related genes, pro-inflammatory cytokines and nitrite production after bacterial infection. Hdac6-/- BMDCs have a weakened phosphorylation of MAPK signalling in response to Lm infection, suggesting altered Toll-like receptor signalling (TLR). Compared with Hdac6+/+ counterparts, Hdac6-/- GM-CSF-derived and FLT3L-derived dendritic cells show weaker pro-inflammatory cytokine secretion in response to various TLR agonists. Moreover, HDAC6 associates with the TLR-adaptor molecule Myeloid differentiation primary response gene 88 (MyD88), and the absence of HDAC6 seems to diminish the NF-κB induction after TLR stimuli. Hdac6-/- mice display low serum levels of inflammatory cytokine IL-6 and correspondingly an increased survival to a systemic infection with Lm. The impaired bacterial clearance in the absence of HDAC6 appears to be caused by a defect in autophagy. Hence, Hdac6-/- BMDCs accumulate higher levels of the autophagy marker p62 and show defective phagosome-lysosome fusion. These data underline the important function of HDAC6 in dendritic cells not only in bacterial autophagy, but also in the proper activation of TLR signalling. These results thus demonstrate an important regulatory role for HDAC6 in the innate immune response to intracellular bacterial infection.
Animals | Autophagy | Dendritic Cells | Female | Histone Deacetylase 6 | Host-Pathogen Interactions | Humans | Interleukin-6 | Listeria monocytogenes | Listeriosis | Male | Mice | Mice, Inbred C57BL | Mice, Knockout | Myeloid Differentiation Factor 88 | Signal Transduction | Toll-Like Receptors | Immunity, Innate
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