The E3 Ubiquitin Protein Ligase LINCR Amplifies the TLR-Mediated Signals through Direct Degradation of MKP1.
Takumi YokosawaSayoko MiyagawaWakana SuzukiYuki NadaYusuke HirataTakuya NoguchiAtsushi MatsuzawaPublished in: Cells (2024)
Toll-like receptors (TLRs) induce innate immune responses through activation of intracellular signaling pathways, such as MAP kinase and NF-κB signaling pathways, and play an important role in host defense against bacterial or viral infections. Meanwhile, excessive activation of TLR signaling leads to a variety of inflammatory disorders, including autoimmune diseases. TLR signaling is therefore strictly controlled to balance optimal immune response and inflammation. However, its balancing mechanisms are not fully understood. In this study, we identified the E3 ubiquitin ligase LINCR/ NEURL3 as a critical regulator of TLR signaling. In LINCR-deficient cells, the sustained activation of JNK and p38 MAPKs induced by the agonists for TLR3, TLR4, and TLR5, was clearly attenuated. Consistent with these observations, TLR-induced production of a series of inflammatory cytokines was significantly attenuated, suggesting that LINCR positively regulates innate immune responses by promoting the activation of JNK and p38. Interestingly, our further mechanistic study identified MAPK phosphatase-1 (MKP1), a negative regulator of MAP kinases, as a ubiquitination target of LINCR. Thus, our results demonstrate that TLRs fine-tune the activation of MAP kinase pathways by balancing LINCR (the positive regulator) and MKP1 (the negative regulator), which may contribute to the induction of optimal immune responses.
Keyphrases
- immune response
- toll like receptor
- signaling pathway
- induced apoptosis
- dendritic cells
- oxidative stress
- inflammatory response
- nuclear factor
- pi k akt
- transcription factor
- cell death
- cell proliferation
- epithelial mesenchymal transition
- body mass index
- high density
- cell cycle arrest
- tyrosine kinase
- physical activity
- air pollution
- amino acid
- weight gain
- endothelial cells
- diabetic rats
- drug induced