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首页> 外文期刊>Japanese Journal of Pharmacology >Enhancement by Ascorbic Acid 2-Glucoside or Repeated Additions of Ascorbate of Mitogen-Induced IgM and IgG Productions by Human Peripheral Blood Lymphocytes
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Enhancement by Ascorbic Acid 2-Glucoside or Repeated Additions of Ascorbate of Mitogen-Induced IgM and IgG Productions by Human Peripheral Blood Lymphocytes

机译:增强的抗坏血酸2-葡萄糖苷或人外周血淋巴细胞反复添加抗坏血酸的丝裂原诱导的IgM和IgG产生

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References(28) Cited-By(7) In this study, the effect of ascorbic acid 2-glucoside (AA-2G), a stable derivative of ascorbic acid (AsA), or repeated additions of ascorbate on antibody productions by human peripheral blood lymphocytes (PBLs) was examined, and the physiological function of AsA was evaluated. When human PBLs were stimulated with Staphylococcus aureus Cowan I or pokeweed mitogen, AA-2G remarkably increased the numbers of IgM- and IgG-secreting cells which were detected by enzyme-linked immunospot assay. Although a single addition of ascorbate was without effect, the effect of AA-2G was remarkably inhibited by the addition of castanospermine, an a-glucosidase inhibitor; and moreover, repeated additions of AsA to the culture medium during the culture period enhanced the response to the same level as did a single addition of AA-2G. These results indicate that AsA has the ability to stimulate the immunoglobulin productions by AA-2G. The phytohemagglutinin-induced proliferative response of PBLs was also stimulated by AA-2G. The intracellular AsA content in PBLs cultured with AA-2G was maintained at relatively high levels during the culture period, whereas the content with a single dose of AsA reached nearly zero by the end of the experiment. These in vitro findings suggest that AA-2G and AsA function as potent immunostimulators of antibody production in humans and that the intracellular AsA content is a key parameter for establishing the immune response of PBLs.
机译:参考文献(28)被引用者(7)在这项研究中,抗坏血酸2-葡萄糖苷(AA-2G),抗坏血酸(AsA)的稳定衍生物或反复添加抗坏血酸对人外周血抗体产生的影响检查了淋巴细胞(PBL),并评估了AsA的生理功能。当用金黄色葡萄球菌Cowan I或商陆有丝分裂原刺激人PBL时,AA-2G显着增加了通过酶联免疫斑点法检测到的分泌IgM和IgG的细胞的数量。尽管单次添加抗坏血酸没有作用,但通过添加α-葡糖苷酶抑制剂粟精胺可显着抑制AA-2G的作用。而且,在培养期间向培养基中反复添加AsA可以将反应提高到与单次添加AA-2G相同的水平。这些结果表明,AsA具有刺激AA-2G产生免疫球蛋白的能力。 AA-2G也刺激了植物血凝素诱导的PBL增殖反应。在培养期间,用AA-2G培养的PBL中的细胞内AsA含量保持在较高水平,而单剂量AsA的含量到实验结束时几乎达到零。这些体外发现表明,AA-2G和AsA可以作为有效的人体抗体免疫刺激剂,而细胞内AsA含量是建立PBL免疫应答的关键参数。

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