Longer differentiation, free of activation signals, might be required for the acquisition of a migratory phenotype in response to later activation; however, such differentiation pattern may not occur in inflamed tissues. Persistent macrophage and DC activation by TLR ligands leads to particularly

powerful inhibitory mechanisms blocking further activation by the same or heterologous stimuli 9. There are several inhibitory factors induced in response to TLR stimulation; it is still unclear, however, how these factors contribute to tolerance for further activation. Some pathways have been connected, like miR146a and IL-10 might both contribute to decreased IRAK1 Dabrafenib expression 11, 21, but the present view supports several coexisting inhibitory pathways in activated DCs and macrophages. Whether these pathways are redundant, additive or synergistic Olaparib solubility dmso or act in different conditions or time frames is yet to be understood. Since DCs developing from monocyte precursors in the inflamed tissues might be particularly affected by the constant presence

of microbial compounds and inflammatory mediators, we decided to study which inhibitory pathways are activated in MoDCs in the presence of early and persistent TLR4 stimulation. We set up an assay distinguishing a timely separated role for the different inhibitory molecules and showed that the LPS-induced SOCS1, STAT3, SLAM, miR146a and IL-10 molecules possessed an immediate effect decreasing the activation induced IL-12 production. None of these molecules, however, played an essential role in the establishment of tolerance to further activation signals. The short-term influence of the tested inhibitory signaling components was probably a consequence of the transient increase in their gene expression or the presence of other, more

efficient inhibitory pathways. Although not tested here, it is also possible that certain Guanylate cyclase 2C inhibitory factors could modulate the expression of particular genes in DCs, thereby inducing a qualitative tuning of cellular functions. Contrary to these pathways, IRAK-1 downregulation, occurring in MoDCs receiving early activation through TLR4 during differentiation, might alone be sufficient to inhibit further activation through TLR molecules, as demonstrated by the strong inhibitory effect of a siRNA induced IRAK-1 downregulation on IL-12 secretion. Previously, SOCS1 has been implicated in establishing tolerance in MoDCs that developed in the presence of TLR4, TLR2 or TLR3 ligands through inhibiting GM-CSF receptor signaling and thereby preventing DC differentiation 11. A blockade of the DC differentiation pathway as a consequence of TLR stimulation on monocyte precursors has also been indicated by other studies, in case of human MoDCs in vitro 27 and in monocytes entering the skin in response to Gram-negative bacteria 28.