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中国精品科技期刊2020
王銮凤,王佳雨,周婉玥,等. 麦胚提取物的制备及其对细胞的增殖活性J. 食品工业科技,2026,47(8):1−10. doi: 10.13386/j.issn1002-0306.2025040009.
引用本文: 王銮凤,王佳雨,周婉玥,等. 麦胚提取物的制备及其对细胞的增殖活性J. 食品工业科技,2026,47(8):1−10. doi: 10.13386/j.issn1002-0306.2025040009.
WANG Luanfeng, WANG Jiayu, ZHOU Wanyue, et al. Preparation of Wheat Germ Extract and Its Proliferative Activity on CellsJ. Science and Technology of Food Industry, 2026, 47(8): 1−10. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025040009.
Citation: WANG Luanfeng, WANG Jiayu, ZHOU Wanyue, et al. Preparation of Wheat Germ Extract and Its Proliferative Activity on CellsJ. Science and Technology of Food Industry, 2026, 47(8): 1−10. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025040009.

麦胚提取物的制备及其对细胞的增殖活性

Preparation of Wheat Germ Extract and Its Proliferative Activity on Cells

  • 摘要: 为实现小麦胚芽的精深加工与高值化利用,本研究制备了麦胚提取物(WGE)并分析了其对细胞增殖活性的影响,利用麦胚无细胞蛋白合成系统制备WGE,进一步采用液相色谱-质谱联用(LC-MS/MS)和高效凝胶渗透色谱法(HPGPC)分析了其中的主要组分,并探究了WGE对RAW264.7细胞和PC12细胞的生长促进作用。并且采用低浓度血清细胞培养和Western blotting挖掘了其促增殖作用的分子机制。结果显示,WGE富含蛋白质与多糖,其中具有蛋白合成调节以及氧化还原酶活性的功能蛋白较多,且主要单糖组成为半乳糖和葡萄糖。WGE对RAW264.7和PC12细胞均具有促增殖作用。在极低浓度血清条件下,能够有效改善RAW264.7细胞和PC12细胞的生长阻滞,其中160 µg/mL的WGE干预可使RAW264.7细胞增殖活性提高了29.26%,PC12细胞增殖活性提高了29.05%。此外,WGE通过增加两种细胞中Ki67与Cyclin-D1蛋白的表达,从而发挥促细胞增殖的作用。WGE可作为天然的功能性细胞生长促进剂,这为小麦胚芽的营养化和功能化应用提供了理论依据。

     

    Abstract: To achieve deep processing and high-value utilization of wheat germ, this study prepared wheat germ extract (WGE) and analyzed its effects on cell proliferation activity. This study prepared WGE using a wheat germ cell-free protein synthesis system. The major components of WGE were further analyzed by LC-MS/MS and HPGPC. Additionally, the growth-promoting effects of WGE on RAW264.7 cells and PC12 cells were investigated. The molecular mechanism underlying its pro-proliferative effect was explored using low-serum cell culture conditions and Western blotting. The results indicated that WGE is rich in proteins and polysaccharides. Among the proteins, those involved in protein synthesis regulation and exhibiting oxidoreductase activity were predominant. The primary monosaccharide components of the polysaccharides were galactose and glucose. WGE exhibited pro-proliferative effects on both RAW264.7 and PC12 cells. Under extremely low serum concentrations, WGE effectively ameliorated growth arrest in both cell types. Treatment with 160 µg/mL WGE increased the proliferation activity of RAW264.7 cells by 29.26% and PC12 cells by 29.05%. Additionally, WGE promoted cell proliferation by upregulating the expression of Ki67 and Cyclin-D1 proteins in both cell lines. These findings demonstrate that WGE can function as a natural, functional cell growth promoter. This study provides a theoretical foundation for the nutraceutical and functional applications of wheat germ.

     

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