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胞壁酰二肽或脂多糖对巨噬细胞超氧阴离子生成活性的双相效应。

Biphasic effects of muramyl dipeptide or lipopolysaccharide on superoxide anion-generating activities of macrophages.

作者信息

Yagawa K, Kaku M, Ichinose Y, Nagao S, Tanaka A, Tomoda A

出版信息

Infect Immun. 1984 Jul;45(1):82-6. doi: 10.1128/iai.45.1.82-86.1984.

Abstract

The superoxide anion (O2-)-generating activity of guinea pig macrophages stimulated by wheat germ agglutinin (WGA), immune complexes, or phorbol myristate acetate (PMA) was studied after short- and long-term exposures of the cells to muramyl dipeptide (MDP) or lipopolysaccharide (LPS). Neither MDP nor LPS alone induced O2- release in macrophages. Short-term (30 min) exposure to these agents caused the enhanced release of O2- in response to WGA or immune complexes, though the PMA-induced O2- generation was not affected. On the other hand, long-term exposure (more than 24 h) to MDP or LPS progressively enhanced O2- generation of the cells induced by WGA, immune complexes, or even PMA. These results suggest that the mechanism for O2- generation of macrophages stimulated by WGA or immune complexes differs from that stimulated by PMA and that the differences also exist between short- and long-term exposure to MDP or LPS.

摘要

在将豚鼠巨噬细胞短期和长期暴露于胞壁酰二肽(MDP)或脂多糖(LPS)后,研究了麦胚凝集素(WGA)、免疫复合物或佛波酯(PMA)刺激下豚鼠巨噬细胞产生超氧阴离子(O2-)的活性。单独的MDP和LPS均未诱导巨噬细胞释放O2-。短期(30分钟)暴露于这些试剂会导致巨噬细胞对WGA或免疫复合物产生的O2-释放增加,不过PMA诱导的O2-生成不受影响。另一方面,长期(超过24小时)暴露于MDP或LPS会逐渐增强WGA、免疫复合物甚至PMA诱导的细胞O2-生成。这些结果表明,WGA或免疫复合物刺激巨噬细胞产生O2-的机制不同于PMA刺激的机制,并且短期和长期暴露于MDP或LPS之间也存在差异。

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