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花生四烯酸氢过氧化物对淋巴细胞有丝分裂的抑制作用。

Inhibition of lymphocyte mitogenesis by an arachidonic acid hydroperoxide.

作者信息

Goodman M G, Weigle W O

出版信息

J Supramol Struct. 1980;13(3):373-83. doi: 10.1002/jss.400130308.

Abstract

Incubation of murine spleen cells with the oxidation product of soybean lipoxidase-treated arachidonic acid results in profound inhibition of induction of proliferation and maturation of these cells. The active entity was shown to be the 15-hydroperoxide of arachidonic acid (15-HPAA). Inhibition of the enzymes of the cyclo-oxygenase pathway fails to disturb this effect, indicating that 15-HPAA is not a substrate for this series of enzymes. 15-HPAA produced in this manner interfered with RNA synthesis, DNA synthesis, and blastogenesis, while failing to exert cytotoxic effects on the cells themselves. A variety of lymphocyte subpopulations, distinguished by their responsiveness to a diverse group of mitogens, were all equally inhibited by the addition of 15-HPAA to culture. Addition of this agent even as late as 24 h after initiation of culture resulted in profound inhibition of the proliferative and differentiative responses of splenic B cells to bacterial lipopolysaccharide (LPS). Exposure of cells to 15-HPAA for 10-30 min was adequate to initiate inhibition, an event that exhibited marked temperature dependence. The effects of pre-incubation with 15-HPAA could not be reversed in its absence in recovery periods of up to 6 h prior to addition of LPS. The implications of these data with reference to cellular activation mechanisms are discussed.

摘要

将小鼠脾细胞与经大豆脂氧化酶处理的花生四烯酸的氧化产物一起孵育,会导致这些细胞的增殖和成熟诱导受到显著抑制。活性物质被证明是花生四烯酸的15-氢过氧化物(15-HPAA)。抑制环氧化酶途径的酶并不能干扰这种效应,这表明15-HPAA不是这一系列酶的底物。以这种方式产生的15-HPAA干扰了RNA合成、DNA合成和细胞增殖,同时对细胞本身没有细胞毒性作用。通过对多种有丝分裂原的反应性区分的各种淋巴细胞亚群,在培养物中添加15-HPAA后均受到同等程度的抑制。即使在培养开始后24小时才添加这种试剂,也会导致脾B细胞对细菌脂多糖(LPS)的增殖和分化反应受到显著抑制。将细胞暴露于15-HPAA 10 - 30分钟就足以启动抑制作用,这一过程表现出明显的温度依赖性。在添加LPS之前长达6小时的恢复期内,在没有15-HPAA的情况下,预先与15-HPAA孵育的效果无法逆转。讨论了这些数据对细胞激活机制的意义。

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