Novel Evidence that Purinergic Signaling - Nlrp3 Inflammasome Axis Regulates Circadian Rhythm of Hematopoietic Stem/Progenitor Cells Circulation in Peripheral Blood.
Mateusz AdamiakAndrzej CiechanowiczMarta SkodaMonika CymerMichal TraczBing XuMariusz Z RatajczakPublished in: Stem cell reviews and reports (2021)
We found that circadian changes in ATP level in peripheral blood (PB) activate the Nlrp3 inflammasome, which triggers diurnal release of hematopoietic stem/progenitor cells (HSPCs) from murine bone marrow (BM) into PB. Consistent with this finding, we observed circadian changes in expression of mRNA for Nlrp3 inflammasome-related genes, including Nlrp3, caspase 1, IL-1β, IL-18, gasdermin (GSDMD), HMGB1, and S100A9. Circadian release of HSPCs from BM into PB as well as expression of Nlrp3-associated genes was decreased in mice in which pannexin 1-mediated secretion of ATP was inhibited by the blocking peptide 10Panx and in animals exposed to the specific small-molecule inhibitor of the Nlrp3 inflammasome MCC950. In addition to HSPCs, a similar decrease in diurnal cell counts was observed for mesenchymal stromal cells (MSCs), endothelial progenitor cells (EPCs), and very small embryonic-like stem cells (VSELs). These results shed more light on the complexity of circadian regulation of HSPC release into PB, which is coordinated in a purinergic signaling-, innate immunity-dependent manner. Moreover, in addition to circadian changes in expression of the Nlrp3 inflammasome we also observed diurnal changes in expression of other inflammasomes, including Aim2, Nrp1a, and Nlrp1b.
Keyphrases
- nlrp inflammasome
- peripheral blood
- poor prognosis
- bone marrow
- stem cells
- heavy metals
- small molecule
- binding protein
- mesenchymal stem cells
- long non coding rna
- endothelial cells
- atrial fibrillation
- cell therapy
- blood pressure
- gene expression
- risk assessment
- single cell
- adipose tissue
- dna methylation
- transcription factor
- cell death
- oxidative stress
- genome wide identification