Regulatory Roles of the Caspase-11 Non-Canonical Inflammasome in Inflammatory Diseases.
Young-Su YiPublished in: Immune network (2018)
Inflammation is an immune response mediated by innate immune cells of tissues, against invading microbes and cellular stress. The hallmark of inflammatory responses is the activation of inflammasomes - multiprotein oligomers comprising intracellular pattern recognition receptors and inflammatory effectors - such as ASC and pro-cysteine-aspartic protease (pro-caspase)-1. Inflammasomes can be classified as canonical or non-canonical, and their activation in response to various ligands commonly induces caspase-1 activation and gasdermin D (GSDMD) processing, leading to caspase-1-mediated maturation and secretion of the pro-inflammatory cytokines IL-1β and IL-18, and GSDMD-mediated pyroptosis through pore generation in cell membranes. Although inflammation protects the host from harmful stimuli, chronic inflammation is a critical risk factor for inflammatory diseases, and several studies have investigated the role of canonical inflammasomes in inflammatory responses and diseases, with emerging studies focusing on the role of non-canonical inflammasomes. This review discusses recent studies on the regulatory roles of the caspase-11 non-canonical inflammasome in the pathogenesis of inflammatory diseases. Additionally, it provides an insight into the development of novel therapeutics based on targeting caspase-11 non-canonical inflammasome and its downstream effectors to prevent and treat human inflammatory conditions.
Keyphrases
- induced apoptosis
- oxidative stress
- cell death
- endoplasmic reticulum stress
- immune response
- cell cycle arrest
- signaling pathway
- innate immune
- transcription factor
- anti inflammatory
- gene expression
- case control
- single cell
- mesenchymal stem cells
- small molecule
- dendritic cells
- inflammatory response
- cell therapy
- mass spectrometry
- stress induced
- type iii
- high resolution