RORγ regulates the NLRP3 inflammasome
| Autor: | Thomas P. Burris, Amer Avdagic, Cyrielle Billon, Meghan H Murray |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
Lipopolysaccharides
0301 basic medicine Lipopolysaccharide Inflammasomes medicine.medical_treatment Interleukin-1beta Galactosamine Response Elements Biochemistry Mice 03 medical and health sciences chemistry.chemical_compound Sepsis NLR Family Pyrin Domain-Containing 3 Protein medicine Animals Molecular Biology Mice Knockout Orphan receptor Innate immune system integumentary system 030102 biochemistry & molecular biology Macrophages Interleukin Inflammasome Cell Biology Liver Failure Acute Nuclear Receptor Subfamily 1 Group F Member 3 Acquired immune system Immunity Innate Cell biology 030104 developmental biology Cytokine chemistry Nuclear receptor Accelerated Communications Th17 Cells medicine.drug |
| Zdroj: | Journal of Biological Chemistry. 294:10-19 |
| ISSN: | 0021-9258 |
| DOI: | 10.1074/jbc.ac118.002127 |
| Popis: | RAR-related orphan receptor γ (RORγ) is a nuclear receptor that plays an essential role in the development of T helper 17 (T(h)17) cells of the adaptive immune system. The NLRP3 inflammasome is a component of the innate immune system that processes interleukin (IL)-1β into a mature cytokine. Elevated activity of the NLRP3 inflammasome contributes to the progression of an array of inflammatory diseases. Bone marrow–derived macrophages (BMDMs) isolated from RORγ-null mice displayed reduced capacity to secrete IL-1β, and they also displayed a reduction in Nlrp3 and Il1b gene expression. Examination of the promoters of the Il1b and Nlrp3 genes revealed multiple putative ROR response elements (ROREs) that were occupied by RORγ. RORγ inverse agonists were effective inhibitors of the inflammasome. RORγ inverse agonists suppressed lipopolysaccharide (LPS)/ATP-stimulated IL-1β secretion and expression of Il1b and Nlrp3 in BMDMs. Additionally, the ability of the RORγ inverse agonists to suppress IL-1β secretion was lost in Nlrp3-null macrophages. The potential for targeting the NLRP3 inflammasome in vivo using RORγ inverse agonists was examined in two models: LPS-induced sepsis and fulminant hepatitis. Pharmacological inhibition of RORγ activity reduced plasma IL-1β as well as IL-1β production by peritoneal macrophages in a model of LPS-induced sepsis. Additionally, RORγ inverse agonists reduced mortality in an LPS/d-galactosamine–induced fulminant hepatitis mouse model. These results illustrate a major role for RORγ in regulation of innate immunity via modulation of NLRP3 inflammasome activity. Furthermore, these data suggest that inhibiting the NLRP3 inflammasome with RORγ inverse agonists may be an effective method to treat NLRP3-associated diseases. |
| Databáze: | OpenAIRE |
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