首页> 外文期刊>The journal of immunology >Separation of Lymphocyte Mitogen from Lymphotoxin and Experiments on the Production of Lymphotoxin by Lymphoid Cells Stimulated with the Partially Purified Mitogen: A Possible Amplification Mechanism of Cellular Immunity and Allergy
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Separation of Lymphocyte Mitogen from Lymphotoxin and Experiments on the Production of Lymphotoxin by Lymphoid Cells Stimulated with the Partially Purified Mitogen: A Possible Amplification Mechanism of Cellular Immunity and Allergy

机译:从淋巴毒素分离淋巴细胞有丝分裂原和部分纯化的有丝分裂原刺激的淋巴样细胞产生淋巴毒素的实验:细胞免疫和过敏的可能放大机制

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A mitogenic factor (MF) from guinea pig lymph node cells (LNC), which was produced by stimulating immune LNC with the specific antigen, ovalbumin, was partially purified by the sequential use of Sephadex G-200 gel filtration, CM-cellulose ion exchange chromatography, DEAE-cellulose ion exchange chromatography, and polyacrylamide disc gel electrophoresis. The product was purified at least 100-fold with regard to protein content. In addition, the purified MF was functionally pure with respect to the absence of lymphotoxin (LT), another guinea pig lymphokine.The possibility that MF, or a substance closely associated with this factor, might serve to amplify cellular immune and allergic reactions by nonspecifically inducing lymphoid cells to produce other lymphokines was then tested by stimulating cells from various lymphoid tissues with the purified MF and assaying the culture fluids for LT activity as a measure of lymphokine production. All the cell types studied incorporated 3H-thymidine in response to purified MF, and some of them produced LT. Thus, spleen cells from normal guinea pigs produced some LT when stimulated with a large dose of MF, but mesenteric LNC produced none. However, mesenteric LNC from guinea pigs that had been immunized by footpad injection of complete Freund's adjuvant (CFA) 10 or 16 days previously produced LT in amounts that were dependent on the stimulating dose of MF. Substantial quantities of LT were produced by cells from peripheral lymph nodes draining the sites of immunization, as well as by spleen cells, the degree of response being dependent on the stimulating dose of MF and the time span after injection of CFA. These results indicate that purified MF, or a substance closely associated with this factor, is capable of inducing LT production by a subset of lymphoid cells that appears to be expanded after immunization. Electrophoretic observations indicated that the induction of LT production may be due to a factor which is distinct from MF although closely similar in molecular size and charge.
机译:通过依次使用Sephadex G-200凝胶过滤,CM-纤维素离子交换,部分纯化了豚鼠淋巴结细胞(LNC)的促有丝分裂因子(MF),该因子是通过用特异性抗原卵清蛋白刺激免疫LNC产生的色谱,DEAE-纤维素离子交换色谱和聚丙烯酰胺圆盘凝胶电泳。就蛋白质含量而言,将产物纯化至少100倍。此外,相对于不存在另一种豚鼠淋巴因子淋巴毒素(LT)而言,纯化的MF在功能上是纯的.MF或与该因子密切相关的物质可能通过非特异性地放大细胞免疫和过敏反应的可能性然后通过用纯化的MF刺激来自各种淋巴组织的细胞并检测培养液的LT活性来衡量诱导淋巴样细胞产生其他淋巴因子的活性,以衡量淋巴因子的产生。所有研究的细胞类型均响应纯化的MF掺入3H-胸苷,其中一些产生LT。因此,正常豚鼠的脾细胞在受到大剂量MF刺激时会产生一些LT,而肠系膜LNC则不会产生。但是,豚鼠肠系膜LNC在10或16天前通过脚垫注射完全弗氏佐剂(CFA)进行了免疫,产生的LT量取决于MF的刺激剂量。大量的LT是由排出免疫部位的外周淋巴结细胞以及脾细胞产生的,应答的程度取决于MF的刺激剂量和注射CFA后的时间跨度。这些结果表明,纯化的MF或与该因子紧密相关的物质能够通过免疫后似乎扩增的淋巴样细胞亚群诱导LT产生。电泳观察表明,诱导LT产生的原因可能是与MF不同的因素,尽管在分子大小和电荷上非常相似。

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