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Regulation of HMGB1 release by inflammasomes
Authors:Ben Lu  Haichao Wang  Ulf Andersson  Kevin J Tracey
Institution:1. Laboratory of Biomedical Science, Feinstein Institute for Medical Research, 350 Community Drive, Manhasset, NY 11030, USA; 2. The Elmezzi Graduate School of Molecular Medicine, North Shore-LIJ Health system, 350 Community Drive, Manhasset, NY 11030, USA; 3. Department of Emergency Medicine, North Shore University Hospital, Manhasset, NY 11030, USA; 4. Department of Women’s and Children’s Health, Karolinska Institutet, S-17677 Stockholm, Sweden
Abstract:High mobility group box 1 (HMGB1) is an evolutionarily conserved non-histone chromatin-binding protein. During infection or injury, activated immune cells and damaged cells release HMGB1 into the extracellular space, where HMGB1 functions as a proinflammatory mediator and contributes importantly to the pathogenesis of infl ammatory diseases. Recent studies reveal that inflammasomes, intracellular protein complexes, critically regulate HMGB1 release from activated immune cells in response to a variety of exogenous and endogenous danger signals. Double stranded RNA dependent kinase (PKR), an intracellular danger-sensing molecule, physically interacts with inflammasome components and is important for inflammasome activation and HMGB1 release. Together, these studies not only unravel novel mechanisms of HMGB1 release during infl ammation, but also provide potential therapeutic targets to treat HMGB1-related infl ammatory diseases.
Keywords:HMGB1  inflammasome  PKR  
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