Key Laboratory of Food Nutrition and Safety of SDNU, Provincial Key Laboratory of Animal, Resistant Biology, College of Life Science, Shandong Normal University, Jinan 250014, China.
State Key Laboratory of Biobased Material and Green Papermaking, Qilu University of Technology, Shandong Academy of Sciences, Jinan 250353, China.
Molecules. 2019 May 13;24(9):1841. doi: 10.3390/molecules24091841.
Many polysaccharides have been shown to be bioactive, with the addition of sulfate often enhancing or altering this bioactivity. In previous studies, masson pine pollen polysaccharides, to include a sulfate derivative, have been shown to promote macrophage proliferation similarly to LPS. However, the exact metabolic mechanisms promoting this proliferation remain unclear. In this study, RAW264.7 macrophage cells were treated with a purified masson pine pollen polysaccharide (PPM60-D), a sulfate derivative (SPPM60-D), or LPS. Proliferation levels at a variety of concentrations were examined using MTT assay, with optimal concentration used when performing metabolomic analysis via H nuclear magnetic resonance (H-NMR). This process resulted in the identification of thirty-five intracellular metabolites. Subsequent multivariate statistical analysis showed that both LPS and SPPM60-D promote RAW264.7 proliferation by promoting aerobic respiration processes and reducing processes associated with glycolysis. While some insight was gained regarding the mechanistic differences between SPPM60-D and LPS, the specific mechanisms governing the effect of SPPM60 on RAW264.7 cells will require further elucidation. These findings show that both LPS and SPPM60-D effectively promote RAW264.7 proliferation and may have beneficial uses in maintaining cellular vitality or inhibiting cancer.
许多多糖已被证明具有生物活性,而添加硫酸酯基团通常会增强或改变这种生物活性。在以前的研究中,已表明马尾松花粉多糖(包括硫酸酯衍生物)可促进巨噬细胞增殖,其作用类似于 LPS。然而,促进这种增殖的确切代谢机制仍不清楚。在这项研究中,用纯化的马尾松花粉多糖(PPM60-D)、硫酸酯衍生物(SPPM60-D)或 LPS 处理 RAW264.7 巨噬细胞。用 MTT 法检测各种浓度下的增殖水平,并用 H 核磁共振(H-NMR)进行代谢组学分析时,使用最佳浓度。这一过程鉴定了三十五个细胞内代谢物。随后的多变量统计分析表明,LPS 和 SPPM60-D 通过促进有氧呼吸过程和降低与糖酵解相关的过程来促进 RAW264.7 增殖。虽然对于 SPPM60-D 和 LPS 之间的机制差异有了一些了解,但 SPPM60 对 RAW264.7 细胞的作用的具体机制仍需要进一步阐明。这些发现表明,LPS 和 SPPM60-D 均可有效促进 RAW264.7 增殖,并可能在维持细胞活力或抑制癌症方面具有有益的用途。