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没食子酸表没食子儿茶素酯(EGCG)通过增强巨噬细胞和 T 细胞和 B 细胞群体的吞噬作用,影响体内的 WEHI-3 白血病小鼠模型。

Epigallocatechin gallate (EGCG), influences a murine WEHI-3 leukemia model in vivo through enhancing phagocytosis of macrophages and populations of T- and B-cells.

机构信息

Department of Nursing, St. Mary's Junior College of Medicine, Nursing and Management, Yilan, Taiwan, ROC.

出版信息

In Vivo. 2013 Sep-Oct;27(5):627-34.

Abstract

Epigallocatechin gallate (EGCG) is the major polyphenol in green tea, and has been reported to have anticancer effects on many types of cancer cells. However, there is no report to show its effects on the immune response in a murine leukemia mouse model. Thus, in the present study, we investigated the effects of EGCG on the immune responses of murine WEHI-3 leukemia cells in vivo. WEHI-3 cells were intraperitoneally injected into normal BALB/c mice to establish leukemic BALB/c mice, which were then oral-treated with or without EGCG at 5, 20 and 40 mg/kg for two weeks. The results indicated that EGCG did not change the weight of the animals, nor the liver or spleen when compared to vehicle (olive oil) -treated groups. Furthermore, EGCG increased the percentage of cluster of differentiation 3 (CD3) (T-cell), cluster of differentiation 19 (CD19) (B-cell) and Macrophage-3 antigen (Mac-3) (macrophage) but reduced the percentage of CD11b (monocyte) cell surface markers in EGCG-treated groups as compared with the untreated leukemia group. EGCG promoted the phagocytosis of macrophages from 5 mg/kg treatment and promoted natural killer cell activity at 40 mg/kg, increased T-cell proliferation at 40 mg/kg but promoted B-cell proliferation at all three doses. Based on these observations, it appears that EGCG might exhibit an immune response in the murine WEHI-3 cell line-induced leukemia in vivo.

摘要

没食子儿茶素没食子酸酯(EGCG)是绿茶中的主要多酚类物质,据报道,它对多种癌细胞具有抗癌作用。然而,目前尚无报道表明其对小鼠白血病模型中的免疫反应有影响。因此,在本研究中,我们研究了 EGCG 对体内 WEHI-3 白血病细胞免疫反应的影响。将 WEHI-3 细胞腹腔内注射到正常 BALB/c 小鼠中,建立白血病 BALB/c 小鼠,然后用 5、20 和 40mg/kg 的 EGCG 进行口服治疗,共两周。结果表明,与载体(橄榄油)处理组相比,EGCG 并未改变动物的体重,也未改变肝脏或脾脏的重量。此外,与未治疗的白血病组相比,EGCG 增加了分化群 3(CD3)(T 细胞)、分化群 19(CD19)(B 细胞)和巨噬细胞-3 抗原(Mac-3)(巨噬细胞)的百分比,而减少了 CD11b(单核细胞)细胞表面标志物的百分比。EGCG 从 5mg/kg 治疗开始促进巨噬细胞的吞噬作用,并在 40mg/kg 时促进自然杀伤细胞活性,在 40mg/kg 时促进 T 细胞增殖,但在所有三个剂量下均促进 B 细胞增殖。基于这些观察结果,EGCG 似乎可能在体内 WEHI-3 细胞系诱导的白血病中表现出免疫反应。

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