首页> 美国卫生研究院文献>Clinical and Diagnostic Laboratory Immunology >Enhancement of Umbilical Cord Blood Cell Hematopoiesis by Maitake Beta-Glucan Is Mediated by Granulocyte Colony-Stimulating Factor Production
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Enhancement of Umbilical Cord Blood Cell Hematopoiesis by Maitake Beta-Glucan Is Mediated by Granulocyte Colony-Stimulating Factor Production

机译:粒细胞集落刺激因子产生介导舞茸β-葡聚糖增强脐带血造血功能

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摘要

Maitake beta-glucan (MBG) is an extract from the fruit body of the Grifola frondosa mushroom that is being widely used to treat cancer in Asia. We have previously reported that MBG enhances mouse bone marrow cell (BMC) hematopoiesis in vitro and protects BMC from doxorubicin (DOX) toxicity. In the current study, we investigated the ability of MBG to enhance hematopoiesis and to reduce the toxic effects of DOX on fresh human umbilical cord blood (CB) cells. MBG treatment significantly enhanced the colony formation unit (CFU) response of granulocytes-macrophages (CFU-GM response) over the whole dose range of 12.5 to 100 μg/ml (P < 0.05). The addition of MBG to DOX-treated CB cells significantly protected granulocyte-macrophage colony formation from the toxicity of DOX, which otherwise produced strong hematopoietic repression. MBG also partially replaced recombinant human granulocyte colony-stimulating factor (rhG-CSF), as shown by a significant augmentation of the CFU-GM response in the absence of rhG-CSF. We found that MBG induces granulocyte colony-stimulating factor (G-CSF) production in CB CD33+ monocytes, as detected by intracellular cytokine flow cytometric assessment. In contrast, we found that adult peripheral blood monocytes did not produce a significant G-CSF response to MBG, whereas both adult and CB monocytes produced G-CSF in response to lipopolysaccharide. These studies provide the first evidence that MBG induces hematopoietic stem cell proliferation and differentiation of CFU-GM in umbilical CB cells and acts directly to induce G-CSF.
机译:舞茸β-葡聚糖(MBG)是从Grifola frondosa蘑菇的果实中提取的,被广泛用于治疗亚洲的癌症。我们以前曾报道过MBG在体外可增强小鼠骨髓细胞(BMC)的造血作用,并保护BMC免受阿霉素(DOX)的毒性。在当前的研究中,我们调查了MBG增强造血功能并降低DOX对新鲜人脐血(CB)细胞的毒性作用的能力。 MBG处理在12.5至100μg/ ml的整个剂量范围内均显着增强了粒细胞-巨噬细胞的集落形成单位(CFU)反应(CFU-GM反应)(P <0.05)。向DOX处理的CB细胞中添加MBG可显着保护粒细胞-巨噬细胞集落形成免受DOX毒性的影响,否则DOX会产生强烈的造血抑制作用。 MBG还部分替代了重组人粒细胞集落刺激因子(rhG-CSF),如在不存在rhG-CSF的情况下CFU-GM反应显着增强所显示。我们发现,通过细胞内细胞因子流式细胞仪检测,MBG可诱导CB CD33 + 单核细胞中粒细胞集落刺激因子(G-CSF)的产生。相反,我们发现成年外周血单核细胞对MBG不会产生显着的G-CSF反应,而成年和CB单核细胞都对脂多糖产生G-CSF。这些研究提供了第一个证据,MBG诱导脐血CB细胞中造血干细胞的增殖和CFU-GM的分化,并直接起到诱导G-CSF的作用。

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