ER stress activates the NLRP3 inflammasome via an UPR-independent pathway

Autor: Annick Mayor, Kazutoshi Mori, Hidenori Ichijo, Rongbin Zhou, Philippe Menu, Aubry Tardivel, J. Tschopp
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Cancer Research
Inflammasomes
medicine.medical_treatment
Interleukin-1beta
Gene Expression
chemistry.chemical_compound
Mice
0302 clinical medicine
RNA
Small Interfering

innate immunity
Mice
Knockout

0303 health sciences
Tunicamycin
Inflammasome
Cell Differentiation
Endoplasmic Reticulum Stress
Cell biology
macrophages
Cytokine
030220 oncology & carcinogenesis
Tetradecanoylphorbol Acetate
Original Article
Signal transduction
medicine.symptom
medicine.drug
Signal Transduction
Immunology
Inflammation
Biology
Proinflammatory cytokine
Cell Line
03 medical and health sciences
Cellular and Molecular Neuroscience
NLR Family
Pyrin Domain-Containing 3 Protein

medicine
Animals
Humans
030304 developmental biology
Endoplasmic reticulum
Lentivirus
Cell Biology
Carrier Proteins/genetics
Carrier Proteins/metabolism
Cell Differentiation/drug effects
Gene Expression/drug effects
Inflammasomes/immunology
Inflammasomes/metabolism
Inflammation/immunology
Inflammation/metabolism
Interleukin-1beta/biosynthesis
Interleukin-1beta/immunology
Potassium/metabolism
RNA
Small Interfering/genetics

Reactive Oxygen Species/metabolism
Signal Transduction/drug effects
Tetradecanoylphorbol Acetate/pharmacology
Tunicamycin/pharmacology
Unfolded Protein Response
NLRP3 inflammasome
chemistry
Unfolded protein response
Potassium
Carrier Proteins
Reactive Oxygen Species
Zdroj: Cell Death and Disease, vol. 3, pp. e261
Cell Death & Disease
Cell Death and Disease; Vol 3
Popis: Uncontrolled endoplasmic reticulum (ER) stress responses are proposed to contribute to the pathology of chronic inflammatory diseases such as type 2 diabetes or atherosclerosis. However, the connection between ER stress and inflammation remains largely unexplored. Here, we show that ER stress causes activation of the NLRP3 inflammasome, with subsequent release of the pro-inflammatory cytokine interleukin-1β. This ER-triggered proinflammatory signal shares the same requirement for reactive oxygen species production and potassium efflux compared with other known NLRP3 inflammasome activators, but is independent of the classical unfolded protein response (UPR). We thus propose that the NLRP3 inflammasome senses and responds to ER stress downstream of a previously uncharacterized ER stress response signaling pathway distinct from the UPR, thus providing mechanistic insight to the link between ER stress and chronic inflammatory diseases.
Databáze: OpenAIRE