RRC ID 89066
Author Zhang H, Zhao Y, Li D, Li H, Wang Z, Zhang L, Niu H, Huang Y, Zhao C, Jin Y, Zhou D.
Title Anti-inflammatory Effects of Membrane Vesicles from Eubacterium rectale via the NLRP3 Signal Pathway.
Journal Probiotics Antimicrob Proteins
Abstract Eubacterium rectale (E. rectale) has the ability to attenuate systemic and intestinal inflammation. Its naturally secreted membrane vesicles (MVs) likely play a crucial role in this process. The objective of this study is to investigate the anti-inflammatory effects of E. rectale and its membrane vesicles (MVs). An inflammation model was established by inducing an inflammatory response in Raw 264.7 cells using lipopolysaccharide (LPS). Subsequently, the cells were pre-treated with E. rectale and its MVs, and the expression levels of IL-1β, IL-6, TNF-α, and IL-10 in the cells were then detected using RT-qPCR. ELISA was used to measure the secretion levels of IL-1β, while western blot analysis was employed to assess the expression of key proteins in the IL-1β pathway, specifically ASC, Caspase 1, and NLRP3. The results revealed that both E. rectale and its MVs significantly reduced the expression of the inflammatory cytokines IL-1β and TNF-α in Raw 264.7 cells, which were induced by LPS. Additionally, they markedly upregulated the expression of the anti-inflammatory cytokine IL-10 and suppressed IL-1β expression via the NLRP3-Caspase 1-ASC signaling pathway. These findings suggest that E. rectale, through its membrane vesicles, can attenuate LPS-induced NLRP3 inflammasome activation, thereby mitigating the inflammatory response in Raw 264.7 cells.
Volume 17(6)
Pages 4841-4850
Published 2025-12-1
DOI 10.1007/s12602-024-10432-y
PII 10.1007/s12602-024-10432-y
PMID 39702738
MeSH Animals Anti-Inflammatory Agents* / metabolism Anti-Inflammatory Agents* / pharmacology Down-Regulation / drug effects Down-Regulation / immunology Eubacterium* / cytology Eubacterium* / metabolism Inflammasomes / drug effects Inflammasomes / immunology Inflammasomes / metabolism Inflammation* / drug therapy Inflammation* / immunology Interleukin-10 / genetics Interleukin-10 / metabolism Interleukin-1beta / genetics Interleukin-1beta / metabolism Lipopolysaccharides / immunology Mice NLR Family, Pyrin Domain-Containing 3 Protein* / metabolism RAW 264.7 Cells Signal Transduction / drug effects Signal Transduction / immunology Tumor Necrosis Factor-alpha / genetics Tumor Necrosis Factor-alpha / metabolism Up-Regulation / drug effects Up-Regulation / immunology
Resource
General Microbes JCM17463