Bodnár Bernadett R, Ghosal Sayam, Kestecher Brachyahu M, Királyhidi Panna, Försönits András, Fekete Nóra, Bugyik Edina, Komlósi Zsolt I, Pállinger Éva, Nagy György, Buzás Edit I, Osteikoetxea Xabier
Institute of Genetics, Cell- and Immunobiology, Semmelweis University, 1089 Budapest, Hungary.
HCEMM-SU Extracellular Vesicles Research Group, 1089 Budapest, Hungary.
Int J Mol Sci. 2025 Jun 25;26(13):6092. doi: 10.3390/ijms26136092.
Extracellular vesicles (EVs) are lipid membrane-enclosed particles released by all cells and can be isolated from various sources, even from solid tissues. This study focuses on isolating and characterizing EVs from mouse lymph nodes (LNs). Male C57BL/6 mice were injected with complete Freund's adjuvant, with or without ovalbumin. Inguinal and popliteal LNs were incised 9 days after immunization, and EV isolation was carried out using a combination of differential centrifugation and size-exclusion chromatography. The characteristic morphology of small and large EVs was confirmed by transmission electron microscopy. Particle size distribution and concentration were determined by nanoparticle tracking analysis, while protein and lipid contents were measured by bicinchoninic acid assay, and sulfo-phospho-vanillin assays, respectively, to calculate the protein-to-lipid ratio. Immune and EV markers were analyzed by using flow cytometry and Western blot assay, revealing significant changes between immunized mice compared to controls. This study establishes a novel protocol for isolating and characterizing EVs from LNs and highlights the impact of immunization on EV properties, offering insights into their roles in immune processes.
细胞外囊泡(EVs)是所有细胞释放的脂质膜包裹颗粒,可从各种来源分离,甚至可从实体组织中分离。本研究聚焦于从小鼠淋巴结(LNs)中分离和鉴定细胞外囊泡。给雄性C57BL/6小鼠注射完全弗氏佐剂,有无卵清蛋白均可。免疫9天后切开腹股沟和腘窝淋巴结,采用差速离心和尺寸排阻色谱相结合的方法进行细胞外囊泡分离。通过透射电子显微镜确认了大小细胞外囊泡的特征形态。通过纳米颗粒跟踪分析确定颗粒大小分布和浓度,同时分别采用二辛可宁酸测定法和磺基磷香草醛测定法测量蛋白质和脂质含量,以计算蛋白质与脂质的比率。通过流式细胞术和蛋白质免疫印迹分析免疫和细胞外囊泡标志物,结果显示与对照组相比,免疫小鼠之间存在显著变化。本研究建立了一种从小鼠淋巴结中分离和鉴定细胞外囊泡的新方案,并突出了免疫对细胞外囊泡特性的影响,为其在免疫过程中的作用提供了见解。