Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5897132 | Cytokine | 2014 | 10 Pages |
Abstract
Pro-inflammatory cytokines are crucial for fighting infection and establishing immunity. Recently, other proteins, such as danger-associated molecular patterns (DAMPs), have also been appreciated for their role in inflammation and immunity. Following the formation and activation of multiprotein complexes, termed inflammasomes, two cytokines, IL-1β and IL-18, along with the DAMP High Mobility Group Box 1 (HMGB1), are released from cells. Although these proteins all lack classical secretion signals and are released by inflammasome activation, they each lead to different downstream consequences. This review examines how various inflammasomes promote the release of IL-1β, IL-18 and HMGB1 to combat pathogenic situations. Each of these effector molecules plays distinct roles during sterile inflammation, responding to viral, bacterial and parasite infection, and tailoring the innate immune response to specific threats.
Keywords
NLRP3NLRCFCASPYDLRRPR3CASP1NlrpMAVSKSHVcaspase-1IAVIFNγRSVNLRRAGECAPSPRRHMGB1TLRDAMPPAMPASCEAEnatural killerexperimental autoimmune encephalomyelitisInflammasomeDanger-associated molecular patternpathogen-associated molecular patterninterferon γinterleukinleucine-rich repeatToll-like receptorpyrin domainCryopyrin-associated periodic syndromescaspase activation and recruitment domainabsent in melanoma 2Influenza A virusRespiratory syncytial virusHigh mobility group box 1 proteinmitochondrial antiviral signaling proteinproteinase 3CARDNod-like receptorReceptor for advanced glycation end productsPattern-recognition receptor
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Authors
Peter A. Keyel,