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- W2789800940 abstract "p38α activation of multiple effectors may underlie the failure of global p38α inhibitors in clinical trials. A unique inhibitor (CDD-450) was developed that selectively blocked p38α activation of the proinflammatory kinase MK2 while sparing p38α activation of PRAK and ATF2. Next, the hypothesis that the p38α–MK2 complex mediates inflammasome priming cues was tested. CDD-450 had no effect on NLRP3 expression, but it decreased IL-1β expression by promoting IL-1β mRNA degradation. Thus, IL-1β is regulated not only transcriptionally by NF-κB and posttranslationally by the inflammasomes but also posttranscriptionally by p38α–MK2. CDD-450 also accelerated TNF-α and IL-6 mRNA decay, inhibited inflammation in mice with cryopyrinopathy, and was as efficacious as global p38α inhibitors in attenuating arthritis in rats and cytokine expression by cells from patients with cryopyrinopathy and rheumatoid arthritis. These findings have clinical translation implications as CDD-450 offers the potential to avoid tachyphylaxis associated with global p38α inhibitors that may result from their inhibition of non-MK2 substrates involved in antiinflammatory and housekeeping responses." @default.
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- W2789800940 date "2018-03-16" @default.
- W2789800940 modified "2023-10-15" @default.
- W2789800940 title "Selective inhibition of the p38α MAPK–MK2 axis inhibits inflammatory cues including inflammasome priming signals" @default.
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- W2789800940 doi "https://doi.org/10.1084/jem.20172063" @default.
- W2789800940 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5940269" @default.
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