Alijagic Andi, Bonura Angela, Barbero Francesco, Puntes Victor F, Gervasi Francesco, Pinsino Annalisa
Consiglio Nazionale delle Ricerche, Istituto per la Ricerca e l'Innovazione Biomedica (IRIB), 90146 Palermo, Italy.
Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Campus UAB, Bellaterra, 08193 Barcelona, Spain.
Nanomaterials (Basel). 2021 Oct 8;11(10):2646. doi: 10.3390/nano11102646.
We investigated the role of the gold nanoparticles functionalized with polyvinylpyrrolidone (PVP-AuNPs) on the innate immune response against an acute infection caused by in an in vitro immunological nonmammalian next-generation model, the sea urchin . To profile the immunomodulatory function of PVP-AuNPs (0.1 μg mL) in sea urchin immune cells stimulated by (10 μg mL) for 3 h, we focused on the baseline immunological state of the donor, and we analysed the topography, cellular metabolism, and expression of human cell surface antigens of the exposed cells, as well as the signalling leading the interaction between PVP-AuNPs and the -stimulated cells. PVP-AuNPs are not able to silence the inflammatory signalling (TLR4/p38MAPK/NF-κB signalling) that involves the whole population of immune cells exposed to . However, our findings emphasise the ability of PVP-AuNPs to stimulate a subset of rare cells (defined here as Group 3) that express CD45 and CD14 antigens on their surface, which are known to be involved in immune cell maturation and macrophage activation in humans. Our evidence on how PVP-AuNPs may stimulate sea urchin immune cells represents an important starting point for planning new research work on the topic.
我们在体外免疫非哺乳动物下一代模型海胆中,研究了用聚乙烯吡咯烷酮功能化的金纳米颗粒(PVP-AuNPs)对由[病原体名称缺失]引起的急性感染的固有免疫反应的作用。为了剖析PVP-AuNPs(0.1μg/mL)在由[病原体名称缺失](10μg/mL)刺激海胆免疫细胞3小时后的免疫调节功能,我们关注供体的基线免疫状态,并分析了暴露细胞的形貌、细胞代谢、人细胞表面抗原的表达,以及导致PVP-AuNPs与[病原体名称缺失]刺激细胞之间相互作用的信号传导。PVP-AuNPs无法使涉及暴露于[病原体名称缺失]的所有海胆免疫细胞群体的炎症信号(TLR4/p38MAPK/NF-κB信号)沉默。然而,我们的研究结果强调了PVP-AuNPs刺激一部分稀有细胞(在此定义为第3组)的能力,这些细胞表面表达CD45和CD14抗原,已知它们参与人类免疫细胞成熟和巨噬细胞活化。我们关于PVP-AuNPs如何刺激海胆免疫细胞的证据是规划该主题新研究工作的重要起点。