Composition for enhancing immunity including ginsenoside f1 as active ingredient
A ginsenoside and immune-enhancing technology are applied in the fields of immune-enhancing pharmaceutical compositions, perforin or granzyme preparation compositions, and immune-enhancing food compositions, and can solve problems such as difficulty in separating rare ginsenosides.
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Embodiment 1
[0079] Example 1: Degranulation activity effect of innate immune cells produced by ginsenoside F1
[0080] The degree of degranulation activity of innate immune cells produced by ginsenoside F1 was determined by flow cytometric analysis (fluorescence activated cell sorter, FACS).
[0081] Specifically, after pretreating peripheral blood mononuclear cells (peripheral blood mononuclear cells, PBMCs) isolated from blood and natural killer cells isolated with ginsenoside, the above cells were combined with K562 cells or 721.221 cells as target cells, respectively. to cultivate. Afterwards, the surface of peripheral blood mononuclear cells and natural killer cells was stained using fluorochrome-conjugated anti-CD3, anti-CD56 and anti-CD107a antibodies. On the other hand, if figure 1 As shown, the degranulation activity of peripheral blood mononuclear cells or natural killer cells is proportional to the expression of CD107a on the cell surface, so the expression of CD107a in peri...
Embodiment 2
[0084] Example 2: Cell killing activity effect of natural killer cells produced by ginsenoside F1
[0085] In order to confirm whether ginsenoside F1 enhances the cell killing activity of natural killer cells, the degree of cytolysis of target cells was measured.
[0086] Specifically, after pretreatment with ginsenoside F1 or Rg3, peripheral blood mononuclear cells (peripheral blood mononuclear cells, PBMC) isolated from blood and simply isolated natural killer cells were mixed with europium-labeled K562 cells or 721.221 cells as target cells were cultured together. The aforementioned natural killer cells and target cells were mixed and cultured at ratios of 5:1, 10:1, 20:1 and 40:1. On the other hand, the degree of fluorescence released from target cells is proportional to the degree of cell-killing activity of natural killer cells. Therefore, after centrifuging the above-mentioned culture solution, use a microplate reader to measure the degree of cell lysis caused by targe...
Embodiment 3
[0088] Example 3: Effect of cell killing activity of primary natural killer cells produced by ginsenoside F1
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