作者: Lionel Luron , David Saliba , Katrina Blazek , Alessandra Lanfrancotti , Irina A. Udalova
关键词: Cancer research 、 HEK 293 cells 、 IκB kinase 、 Cytokine 、 Transcription factor 、 Cell biology 、 FOXO3 、 TLR4 、 Biology 、 Interferon regulatory factors 、 Interferon
摘要: Cell survival transcription factor FOXO3 has been recently implicated in moderating pro-inflammatory cytokine production by dendritic cells (DCs), but the molecular mechanisms are unclear. It was suggested that could antagonize NF-κB activity, while IKK-β demonstrated to inactivate FOXO3, suggesting a cross-talk between two pathways. Therefore, activity must be tightly regulated allow for an appropriate inflammatory response. Here, we show human monocyte-derived DCs (MDDCs), is able signaling intermediates downstream of Toll-like receptor (TLR) 4, such as and interferon regulatory factors (IRFs), resulting inhibition (IFN)-β expression. We also demonstrate itself IKK-e, kinase involved IFN-β production, which phosphorylates inactivates response TLR4 agonists. Thus, identify new IKK-e-controlled check-point IRF activation regulation expression, providing insight into role immune control.