首页> 外文期刊>Mediators of inflammation >Establishment of a consistent L929 bioassay system for TNF-α quantitation to evaluate the effect of lipopolysaccharide, phytomitogens and cytodifferentiation agents on cytotoxicity of TNF-α secreted by adherent human mononuclear cells
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Establishment of a consistent L929 bioassay system for TNF-α quantitation to evaluate the effect of lipopolysaccharide, phytomitogens and cytodifferentiation agents on cytotoxicity of TNF-α secreted by adherent human mononuclear cells

机译:建立一致的L929生物测定系统以进行TNF-α定量,以评估脂多糖,植物分裂原和细胞分化剂对人黏附单核细胞分泌的TNF-α的细胞毒性的影响

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Tumor necrosis factor-α (TNF-α ) plays an important role in the pathogenesis of rheumatoid arthritis. The present study was to evaluate the effects of lipopolysaccharide (LPS), phytomitogens and cytodifferentiation agents on cytotoxicity of TNF-α secreted by adherent human mononuclear cells (AMC). TNF-α cytotoxicity in LPS-treated, phytomitogen-treated, and cytodifferentiation agent-treated AMC supernatants were analyzed by the L929 bioassay system. Our results showed that LPS could induce homogeneous TNF-α production by AMC whereas, in addition to TNF-α, phytomitogens could also induce other TNF-like factors. Neither methotrexate, retinoic acid nor sodium butyrate can inhibit TNF-α cytotoxicity, while hexamethylene bisacetamide could not only inhibit TNF-α cytotoxicity but also TNF-α inducing ability of LPS to AMC.
机译:肿瘤坏死因子-α(TNF-α)在类风湿关节炎的发病机理中起着重要作用。本研究旨在评估脂多糖(LPS),植物分裂素和细胞分化剂对人黏附单核细胞(AMC)分泌的TNF-α的细胞毒性的影响。通过L929生物测定系统分析了LPS处理,植物分裂素处理和细胞分化剂处理的AMC上清液中TNF-α的细胞毒性。我们的研究结果表明,LPS可以诱导AMC产生均质的TNF-α,而除TNF-α之外,植物分裂原还可以诱导其他类似TNF的因子。甲氨蝶呤,视黄酸或丁酸钠均不能抑制TNF-α的细胞毒性,而六亚甲基双乙酰胺不仅可以抑制TNF-α的细胞毒性,而且可以抑制LPS对AMC的TNF-α诱导能力。

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