2019
DOI: 10.3389/fimmu.2019.01284
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Evaluation of Canonical Inflammasome Activation in Human Monocytes by Imaging Flow Cytometry

Abstract: Canonical inflammasome activation is a tightly regulated process that has been implicated in a broad spectrum of inflammatory disorders. Inflammasome formation requires assembly of a cytosolic sensor protein with the adapter, ASC (apoptosis-associated speck-like protein containing a caspase activating and recruitment domain). Once formed, this multimeric protein structure allows for the activation of caspase-1, responsible for IL-1ß/IL-18 release. During this process, cytoplasmic dispersed ASC molecules cluste… Show more

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Cited by 25 publications
(24 citation statements)
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“…This results in a highly inflammatory form of cell death that goes beyond the release of pro-inflammatory cytokines to include the release of other cytosolic proteins. Consistent with multiple reports, our study confirms that MNC and microglia actively release pyroptosis-related proteins into the extracellular space 20,21,85,86 . We have extended these previous studies, finding pyroptosis-related proteins in human plasma samples and an association between elevated levels of circulating NLRP3 and PD.…”
Section: Discussionsupporting
confidence: 92%
“…This results in a highly inflammatory form of cell death that goes beyond the release of pro-inflammatory cytokines to include the release of other cytosolic proteins. Consistent with multiple reports, our study confirms that MNC and microglia actively release pyroptosis-related proteins into the extracellular space 20,21,85,86 . We have extended these previous studies, finding pyroptosis-related proteins in human plasma samples and an association between elevated levels of circulating NLRP3 and PD.…”
Section: Discussionsupporting
confidence: 92%
“…Canonical inflammasomes, such as NLRP3, are composed of a sensor protein that can recruit caspase-1 activating machinery, usually via the adaptor molecule ASC [Apoptosis-associated speck-like protein containing a caspase recruitment domain (CARD)]. During inflammasome activation, spatial re-localization of ASC into punctate structures has been described in response to stimuli ( 43 , 44 ). To evaluate if BpOMVs promote ASC speck formation, THP1-ASC-GFP cells were stimulated with BpOMVs.…”
Section: Resultsmentioning
confidence: 99%
“…Cells were washed in FACS buffer, blocked, stained, and fixed as above. This assay employs the fluorescent inhibitor probe FAM-YVAD-FMK to label active caspase-1 enzyme in living cells (Lage et al, 2019). For Intracellular cytokine production analysis, before staining 1 l of GolgiPlug containing brefeldin A (BD Biosciences) was added to 800 l of complete RPMI, and cells were incubated for 2 h at 37°C (5% CO 2 ).…”
Section: Molecular and Cellular Analysismentioning
confidence: 99%