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DL-α-二氟甲基鸟氨酸和甲基乙二醛双(脒腙)对植物血凝素激活的人淋巴细胞中多胺和大分子形成的抑制作用

Suppression of the formation of polyamines and macromolecules by DL-alpha-difluoromethylornithine and methylglyoxal bis(guanylhydrazone) in phytohaemagglutinin-activated human lymphocytes.

作者信息

Hölttä E, Jänne J, Hovi T

出版信息

Biochem J. 1979 Jan 15;178(1):109-17. doi: 10.1042/bj1780109.

Abstract
  1. The activation of human peripheral blood lymphocytes by phytohaemagglutinin in vitro was accompanied by striking increases in the concentrations of the natural polyamines putrescine, spermidine and spermine. 2. The enhanced accumulation of polyamines could be almost totally abolished by dl-alpha-difluoromethylornithine, a newly discovered irreversible inhibitor of l-ornithine decarboxylase (EC 4.1.1.17), or by methylglyoxal bis(guanylhydrazone) {1,1'-[(methylethanediylidene)dinitrilo]diguanidine}, an inhibitor of S-adenosyl-l-methionine decarboxylase (EC 4.1.1.50). The inhibition of polyamine accumulation was associated with a marked suppression of DNA synthesis, which was partially or totally reversed by low concentrations of exogenous putrescine, spermidine, spermine and cadaverine and by higher concentrations of 1,3-diaminopropane. 3. In contrast with some earlier studies, we found that methylglyoxal bis(guanylhydrazone), at concentrations that were sufficient to prevent polyamine accumulation, also caused a clear inhibition of protein synthesis in the activated lymphocytes. Similar results were obtained with difluoromethylornithine. The decrease in protein synthesis caused by both compounds preceded the impairment of DNA synthesis. The inhibition of protein synthesis by difluoromethylornithine was fully reversed by exogenous putrescine, spermidine and spermine, and that caused by methylglyoxal bis(guanylhydrazone) by spermidine and spermine. In further support of the idea that the inhibition of protein synthesis by these compounds was related to the polyamine depletion, we found that difluoromethylornithine caused a dose-dependent decrease in the incorporation of [(14)C]leucine into lymphocyte proteins which closely correlated with the decreased concentrations of cellular spermidine. 4. Difluoromethylornithine and methylglyoxal bis(guanylhydrazone) also elicited a variable depression in the incorporation of [(3)H]uridine and [(14)C]adenine into total RNA. The apparent turnover of lymphocyte RNA remained essentially unchanged in spite of severe polyamine depletion brought about by difluoromethylornithine. 5. The present results, as well as confirming the anti-proliferative action of the inhibitors of polyamine biosynthesis, suggest that polyamine depletion may interfere with reactions at different levels of gene expression.
摘要
  1. 体外植物血凝素激活人外周血淋巴细胞时,天然多胺腐胺、亚精胺和精胺的浓度显著增加。2. 新发现的不可逆的L-鸟氨酸脱羧酶(EC 4.1.1.17)抑制剂dl-α-二氟甲基鸟氨酸,或S-腺苷-L-甲硫氨酸脱羧酶(EC 4.1.1.50)抑制剂甲基乙二醛双(脒基腙){1,1'-[(甲基乙二亚基)二腈基]二胍},几乎可完全消除多胺的积累增强。多胺积累的抑制与DNA合成的显著抑制相关,低浓度的外源性腐胺、亚精胺、精胺和尸胺以及高浓度的1,3-二氨基丙烷可部分或完全逆转这种抑制。3. 与一些早期研究不同,我们发现,甲基乙二醛双(脒基腙)在足以阻止多胺积累的浓度下,也会明显抑制活化淋巴细胞中的蛋白质合成。二氟甲基鸟氨酸也得到了类似结果。两种化合物引起的蛋白质合成减少先于DNA合成受损。二氟甲基鸟氨酸对蛋白质合成的抑制可被外源性腐胺、亚精胺和精胺完全逆转,甲基乙二醛双(脒基腙)引起的抑制可被亚精胺和精胺逆转。为进一步支持这些化合物对蛋白质合成的抑制与多胺耗竭有关的观点,我们发现二氟甲基鸟氨酸导致[(14)C]亮氨酸掺入淋巴细胞蛋白质的量呈剂量依赖性减少,这与细胞内亚精胺浓度降低密切相关。4. 二氟甲基鸟氨酸和甲基乙二醛双(脒基腙)也使[(3)H]尿苷和[(14)C]腺嘌呤掺入总RNA的量出现不同程度的降低。尽管二氟甲基鸟氨酸导致严重的多胺耗竭,但淋巴细胞RNA的表观周转率基本保持不变。5. 本研究结果不仅证实了多胺生物合成抑制剂的抗增殖作用,还表明多胺耗竭可能干扰基因表达不同水平的反应。

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