Sandanusova Miriam, Turkova Kristyna, Pechackova Eva, Kotoucek Jan, Roudnicky Pavel, Sindelar Martin, Kubala Lukas, Ambrozova Gabriela
Faculty of Science, Department of Experimental Biology Masaryk University Brno Czech Republic.
Department of Biophysics of Immune System Institute of Biophysics of the Czech Academy of Sciences Brno Czech Republic.
J Extracell Biol. 2024 Aug 22;3(8):e169. doi: 10.1002/jex2.169. eCollection 2024 Aug.
Lipid bi-layered particles known as membrane vesicles (MVs), produced by Gram-positive bacteria are a communication tool throughout the entire bacterial growth. However, the MVs characteristics may vary across all stages of maternal culture growth, leading to inconsistencies in MVs research. This, in turn, hinders their employment as nanocarriers, vaccines and other medical applications. In this study, we aimed to comprehensively characterize MVs derived from CCM7091 isolated at different growth stages: early exponential (6 h, MV6), late exponential (12 h, MV12) and late stationary phase (48 h, MV48). We observed significant differences in protein content between MV6 and MV48 (data are available via ProteomeXchange with identifier PXD041580), likely contributing to their different immunomodulatory capacities. In vitro analysis demonstrated that MV48 uptake rate by epithelial Caco-2 cells is significantly higher and they stimulate an immune response in murine macrophages RAW 264.7 (elevated production of TNFα, IL-6, IL-10, NO). This correlated with increased expression of lipoteichoic acid (LTA) and enhanced TLR2 signalling in MV48, suggesting that LTA contributes to the immunomodulation. In conclusion, we showed that CCM7091-derived MVs from the late stationary phase boost the immune response the most effectively, which pre-destines them for therapeutical application as nanocarriers.
革兰氏阳性菌产生的被称为膜泡(MVs)的脂质双分子层颗粒是细菌整个生长过程中的一种通讯工具。然而,母本培养物生长的各个阶段中MVs的特性可能会有所不同,导致MVs研究结果不一致。这反过来又阻碍了它们作为纳米载体、疫苗及其他医学应用的使用。在本研究中,我们旨在全面表征从处于不同生长阶段分离得到的CCM7091所产生的MVs:指数前期(6小时,MV6)、指数后期(12小时,MV12)和稳定后期(48小时,MV48)。我们观察到MV6和MV48之间蛋白质含量存在显著差异(数据可通过ProteomeXchange获得,标识符为PXD041580),这可能导致它们具有不同的免疫调节能力。体外分析表明,上皮Caco-2细胞对MV48的摄取率显著更高,并且它们能刺激小鼠巨噬细胞RAW 264.7产生免疫反应(TNFα、IL-6、IL-10、NO的产生增加)。这与MV48中脂磷壁酸(LTA)表达增加及TLR2信号增强相关,表明LTA有助于免疫调节。总之,我们表明来自稳定后期的CCM7091衍生的MVs最有效地增强了免疫反应,这使其注定可作为纳米载体用于治疗应用。