Department of Biochemistry and Applied Biosciences, University of Miyazaki, 1-1 Gakuenkibanadai-nishi, Miyazaki 889-2192, Japan.
Faculty of Regional Innovation, University of Miyazaki, 1-1 Gakuenkibanadai-nishi, Miyazaki 889-2192, Japan.
Molecules. 2021 May 7;26(9):2763. doi: 10.3390/molecules26092763.
The aim of this study was to evaluate the involvement of nanoparticles prepared from L. as anti-inflammatory agents. In the present study, we identified nanoparticles from L. using the ultracentrifugation exosome purification method. The nanoparticles were referred to as 17,000× and 200,000× precipitates, and they contained quercetins, proteins, lipids, and small-sized RNA. The nanoparticles inhibited nitric oxide production from lipopolysaccharide (LPS)-stimulated RAW264 cells without cytotoxic properties. Cellular incorporation was confirmed by laser microscopic observation after PKH26 staining. The inhibition of caveolae-dependent endocytosis and macropinocytosis significantly prevented the incorporation of the nanoparticles but had no effect on the inhibition of nitric oxide in RAW264 cells. Collectively, the identified nanoparticles were capable of inhibiting the LPS response via extracellular mechanisms. Taken together, the way of consuming L. without collapsing the nanoparticles is expected to provide an efficient anti-inflammatory effect.
本研究旨在评估从 L. 中制备的纳米粒子作为抗炎剂的作用。在本研究中,我们使用超速离心外泌体纯化方法从 L. 中鉴定出纳米粒子。这些纳米粒子被称为 17,000× 和 200,000× 沉淀物,它们含有槲皮素、蛋白质、脂质和小 RNA。这些纳米粒子抑制了脂多糖(LPS)刺激的 RAW264 细胞中一氧化氮的产生,同时没有细胞毒性。通过 PKH26 染色后的激光显微镜观察证实了细胞摄取。抑制 caveolae 依赖性内吞作用和巨胞饮作用显著阻止了纳米粒子的摄取,但对 RAW264 细胞中一氧化氮的抑制没有影响。综上所述,鉴定出的纳米粒子能够通过细胞外机制抑制 LPS 反应。总的来说,不破坏纳米粒子的 L. 摄取方式有望提供有效的抗炎作用。