International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(11), С. 5069 - 5069
Опубликована: Май 24, 2025
Activation of cGAS, a cytosolic receptor recognizing double-stranded DNA, in macrophages is important sepsis (a life-threatening condition caused by infection). The responses against induced subcutaneous implantation the Pseudomonas-contaminated catheters cGAS-deficient (cGAS−/−) mice were lower than wild-type (WT) as indicated liver enzymes, white blood cell count, cytokines, and M1-polarized spleens. Likewise, lethal dose lipopolysaccharide (LPS) less severe severity determined mortality, organ injury, cell-free serum cytokines. Patterns transcriptome (LPS)-stimulated bone marrow-derived clearly different between cGAS−/− WT cells. Gene set enrichment analysis (GSEA; computational statistical determination gene set) more prominent oxidative phosphorylation (OXPHOS; mitochondrial function) mTORC1 pathways LPS-activated compared with WT. Meanwhile, LPS upregulated cGAS increased cGAMP inducer) only along inflammation macrophages, supernatant pro-inflammatory molecules (nuclear factor kappa B; NF-κB), M1 polarization (IL-1β, CD80, CD86), macrophage extracellular traps (METs; web-like structures composed histones, other proteins) through detection citrullinated histone 3 (CitH3) immunofluorescent visualization. In conclusion, demonstrated (catheter-induced injection model) vitro (transcriptomic analysis, polarization, METs).
Язык: Английский