Pediococcus pentosaceus-derived Exosome Research and Application
Pediococcus pentosaceus is a Gram-positive bacterium belonging to the group of lactic acid bacteria, which is one of the common beneficial bacteria in the food fermentation process. In recent years, there has been a gradual increase in exosome-like vesicles of Pediococcus pentosaceus source to regulate inflammatory functions and related studies. Creative Biolabs has accumulated insights into gram-positive bacteria, including Pediococcus pentosaceus, and can provide customized research services on bacterial-derived exosomes.
Isolation of Exosomes from Pediococcus pentosaceus
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Culture Pediococcus pentosaceus in medium overnight at 37°C and then collect the supernatant.
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Centrifuge at low speed and then filter the Pediococcus pentosaceus supernatant with filters.
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After the filter, centrifuge the Pediococcus pentosaceus supernatant several times at ultra-high speed.
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Resuspend the centrifuged Pediococcus pentosaceus exosome precipitate with sterile PBS and store frozen.
Studies on Pediococcus pentosaceus-derived Exosomes
Study
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Conclusion
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Characterization of Pediococcus pentosaceus-derived exosomes.
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Compared to E. coli-derived extracellular vesicles, exosomes derived from human intestinal commensals, including Pediococcus pentosaceus, had larger sizes. In addition, disposable capillary cell assay showed that Pediococcus pentosaceus-derived exosomes exhibited high negative electronegativity.
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Therapeutic effects of Pediococcus pentosaceus-derived exosomes in liver fibrosis models and vaccination models.
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Pediococcus pentosaceus-derived exosomes ameliorated hepatic fibrosis pathology in inflammation-induced mouse models.
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Pediococcus pentosaceus-derived exosomes negatively regulate vaccine-induced immune responses by inhibiting Th1 cells.
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Effects of Pediococcus pentosaceus-derived exosomes on immune cells.
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Differentiation of myeloid derived suppressor cells from bone marrow precursors was promoted in mice injected intraperitoneally with Pediococcus pentosaceus-derived exosomes.
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Treatment with Pediococcus pentosaceus-derived exosomes was capable of inducing myeloid-derived macrophage polarization toward an M2-like immunosuppressive phenotype, inhibiting T-cell activation, and strongly promoting the expression of IL-10, arginase-1, and PD-L1.
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The results of neutralizing antibody blocking assays showed that this immunomodulatory activity of Pediococcus pentosaceus exosomes was mediated by TLR2.
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Effects of Pediococcus pentosaceus-derived exosomes on inflammation-related diseases and wound healing.
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Treatment with Pediococcus pentosaceus-derived exosomes reduced the level of neutrophil accumulation in the peritoneal cavity in models of acute peritonitis in mice.
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Assays of chemical-induced mouse colitis models also showed that Pediococcus pentosaceus-derived exosomes protected against and mitigated inflammation.
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In mouse skin wound models, intraperitoneal injection of Pediococcus pentosaceus exosomes reduced inflammatory cell infiltration and recruited more MDSC to the wound to favor wound healing.
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Fig. 1 Pediococcus pentosaceus-derived exosomes modulate inflammation and therapeutic potential for inflammation-related diseases.1
It has been shown that Pediococcus pentosaceus-derived exosomes can possess potential therapeutic effects on inflammation-related diseases by modulating inflammation-related signaling pathways, influencing immune cell activity, and improving the balance of intestinal flora, etc. Creative Biolabs has a comprehensive platform for exosome research to facilitate a deeper understanding of Pediococcus pentosaceus-derived exosomes. Please contact us with your project demands.
Reference
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Alpdundar Bulut, Esin, et al. "Human gut commensal membrane vesicles modulate inflammation by generating M2-like macrophages and myeloid-derived suppressor cells." The Journal of Immunology 205.10 (2020): 2707-2718.
For Research Use Only. Cannot be used by patients.
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