Autor(es): Rodrigues, Fernando ; Pedrosa, Jorge ; Coelho, Maria Teixeira ; Guedes, Joana ; Ferreirinha, Pedro ; Howes, Ashleigh ; Lai, Wi S. ; Blackshear, Perry J. ; O´Garra, Anne ; Castro, António G. ; Saraiva, Margarida
Data: 2014
Identificador Persistente: https://hdl.handle.net/1822/33098
Origem: RepositóriUM - Universidade do Minho
Assunto(s): IL-10; MAPKs; TLRs; Post-transcriptional regulation
The activation of TLRs by microbial molecules triggers intracellular-signaling cascades and the expression of cytokines such as IL-10. Il10 expression is tightly controlled to ensure effective immune responses, while preventing pathology. Maximal TLR-induction of Il10 transcription in macrophages requires signaling through the MAPKs, ERK, and p38. Signals via p38 downstream of TLR4 activation also regulate IL-10 at the post-transcriptional level, but whether this mechanism operates downstream of other TLRs is not clear. We compared the regulation of IL-10 production in TLR2 and TLR4-stimulated BM-derived macrophages and found different stability profiles for the Il10 mRNA. TLR2 signals promoted a rapid induction and degradation of Il10 mRNA, whereas TLR4 signals protected Il10 mRNA from rapid degradation, due to the activation of Toll/IL-1 receptor domain-containing adaptor inducing IFN-ß (TRIF) and enhanced p38 signaling. This differential post-transcriptional mechanism contributes to a stronger induction of IL-10 secretion via TLR4. Our study provides a molecular mechanism for the differential IL-10 production by TLR2- or TLR4-stimulated BMMs, showing that p38-induced stability is not common to all TLR-signaling pathways. This mechanism is also observed upon bacterial activation of TLR2 or TLR4 in BMMs, contributing to IL-10 modulation in these cells in an infection setting.
