| Literature DB >> 28109721 |
Meghana N Patel1, Richard G Carroll2, Silvia Galván-Peña2, Evanna L Mills2, Robin Olden3, Martha Triantafilou3, Amaya I Wolf4, Clare E Bryant5, Kathy Triantafilou3, Seth L Masters6.
Abstract
The inflammasome is a cytoplasmic protein complex that processes interleukins (IL)-1β and IL-18, and drives a form of cell death known as pyroptosis. Oligomerization of this complex is actually the second step of activation, and a priming step must occur first. This involves transcriptional upregulation of pro-IL-1β, inflammasome sensor NLRP3, or the non-canonical inflammasome sensor caspase-11. An additional aspect of priming is the post-translational modification of particular inflammasome constituents. Priming is typically accomplished in vitro using a microbial Toll-like receptor (TLR) ligand. However, it is now clear that inflammasomes are activated during the progression of sterile inflammatory diseases such as atherosclerosis, metabolic disease, and neuroinflammatory disorders. Therefore, it is time to consider the endogenous factors and mechanisms that may prime the inflammasome in these conditions.Entities:
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Year: 2017 PMID: 28109721 DOI: 10.1016/j.molmed.2016.12.007
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951