Department of Animal Health, Istituto Zooprofilattico Sperimentale della Sardegna, Sassari, Italy.
Department of Veterinary Medicine, University of Perugia, Perugia, Italy.
Front Immunol. 2023 Jun 16;14:1209898. doi: 10.3389/fimmu.2023.1209898. eCollection 2023.
Extracellular vesicles (EVs) are nanometric-membrane-bound sub-cellular structures, which can be recovered from milk. Milk EVs have drawn increasing interest due to their potential biomedical applications, therefore it is important to investigate their impact on key immune cells, such as macrophages.
In this work, the immunomodulatory effects of goat milk EVs on untreated (moMФ) and classically activated (moM1) porcine monocyte-derived macrophages were investigated using flow cytometry, ELISA, and gene expression assays.
These particles were efficiently internalized by macrophages and high doses (60 mg protein weight) triggered the upregulation of MHC I and MHC II DR on moMФ, but not on moM1. In moMФ, exposure to low doses (0.6 mg) of mEVs enhanced the gene expression of IL10, EBI3, and IFNB, whereas high doses up-regulated several pro-inflammatory cytokines. These nanosized structures slightly modulated cytokine gene expression on moM1. Accordingly, the cytokine (protein) contents in culture supernatants of moMФ were mildly affected by exposure to low doses of mEVs, whereas high doses promoted the increased release of TNF, IL-8, IL-1a, IL-1b, IL-1Ra, IL-6, IL-10, and IL-12. The cytokines content in moM1 supernatants was not critically affected.
Overall, our data support a clinical application of these molecules: they polarized macrophages toward an M1-like phenotype, but this activation seemed to be controlled, to prevent potentially pathological over-reaction to stressors.
细胞外囊泡(EVs)是纳米级膜结合的细胞亚结构,可以从牛奶中回收。由于其在生物医学中的潜在应用,牛奶 EVs 引起了越来越多的关注,因此研究其对关键免疫细胞(如巨噬细胞)的影响非常重要。
在这项工作中,使用流式细胞术、ELISA 和基因表达分析研究了山羊奶 EVs 对未经处理(moMФ)和经典激活(moM1)猪单核细胞衍生巨噬细胞的免疫调节作用。
这些颗粒被巨噬细胞有效内化,高剂量(60 毫克蛋白质重量)触发 moMФ 上 MHC I 和 MHC II DR 的上调,但在 moM1 上没有。在 moMФ 中,低剂量(0.6 毫克)的 mEVs 暴露增强了 IL10、EBI3 和 IFNB 的基因表达,而高剂量则上调了几种促炎细胞因子。这些纳米结构对 moM1 的细胞因子基因表达略有调节。相应地,moMФ 培养上清液中的细胞因子(蛋白)含量受到 mEVs 低剂量暴露的轻微影响,而高剂量则促进 TNF、IL-8、IL-1a、IL-1b、IL-1Ra、IL-6、IL-10 和 IL-12 的释放增加。moM1 上清液中的细胞因子含量没有受到严重影响。
总的来说,我们的数据支持这些分子的临床应用:它们将巨噬细胞极化为 M1 样表型,但这种激活似乎受到控制,以防止对应激源产生潜在的病理性过度反应。