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Ganoderma lucidum polysaccharides counteract inhibition on CD71 and FasL expression by culture supernatant of B16F10 cells upon lymphocyte activation

机译:灵芝多糖抵消淋巴细胞活化后B16F10细胞培养上清对CD71和FasL表达的抑制作用

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摘要

Immune responses to tumor-associated antigens are often detectable in tumor-bearing hosts, but they fail to eliminate malignant cells or prevent development of metastases. Tumor cells produce factors such as interleukin-10, transforming growth factor-beta 1 and vascular endothelial growth factor (VEGF) that suppress the function of immune cells or induce apoptosis of immune cells. Culture supernatant of tumor cells may contain these immunosuppressive factors which suppress lymphocyte activation. CD71 and FasL are two important molecules that are expressed upon lymphocyte activation. Counteraction against suppression CD71 and FasL expression upon lymphocyte activation may benefit tumor control. A potential component with this effect is Ganoderma lucidum polysaccharides (Gl-PS). In this study, Gl-PS was used on lymphocytes incubating with culture supernatant of B16F10 melanoma cells (B16F10-CS) in the presence of phytohemagglutinin. Following induction with phytohemagglutinin, B16F10-CS suppressed CD71 expression in lymphocytes (as detected by immunofluorescence and flow cytometry), proliferation in lymphocytes (as detected by MTT assay), and FasL expression in lymphocytes (as detected by immunocytochemistry and western blot analysis), while Gl-PS fully or partially counteracted these suppressions. Gl-PS showed counteractive effects against suppression induced by B16F10-CS on CD71 and FasL expression upon lymphocyte activation, suggesting the potential of Gl-PS to facilitate cancer immunotherapy.
机译:在携带肿瘤的宿主中通常可以检测到对肿瘤相关抗原的免疫反应,但是它们不能消除恶性细胞或阻止转移的发展。肿瘤细胞产生的因子如白介素10,转化生长因子β1和血管内皮生长因子(VEGF),可抑制免疫细胞的功能或诱导免疫细胞的凋亡。肿瘤细胞的培养上清液可能含有抑制淋巴细胞活化的这些免疫抑制因子。 CD71和FasL是在淋巴细胞激活后表达的两个重要分子。抑制淋巴细胞激活后抑制CD71和FasL表达的反作用可能有益于肿瘤控制。具有这种作用的潜在成分是灵芝多糖(G1-PS)。在这项研究中,Gl-PS用于在存在植物血凝素的情况下与B16F10黑色素瘤细胞(B16F10-CS)的培养上清液一起孵育的淋巴细胞。在用植物血凝素诱导后,B16F10-CS抑制了淋巴细胞中CD71的表达(通过免疫荧光和流式细胞术检测),淋巴细胞的增殖(通过MTT分析检测)和淋巴细胞中FasL的表达(通过免疫细胞化学和蛋白质印迹分析检测),而G1-PS完全或部分抵消了这些抑制作用。 G1-PS对淋巴细胞活化后B16F10-CS诱导的抑制CD71和FasL表达具有抑制作用,表明G1-PS促进癌症免疫治疗的潜力。

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