在小鼠癌症腹水中发现高含量的低分子量免疫抑制因子。2. 从癌症腹水中分离的1-甲基腺苷增强小鼠李斯特菌感染。

S Takano, S Sami, T Majima, N Ishida
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引用次数: 21

摘要

已知埃利希癌腹水的低分子量分数(mol wt小于1000)可增强小鼠的李斯特菌感染。化学表征表明该组分中存在4种嘌呤和嘧啶类似物,即尿酸、尿嘧啶、假尿嘧啶和1-甲基腺苷(m1Ado)。当研究这些成分对小鼠李斯特菌感染的影响时,只有m1Ado显著增强了感染并在短时间内杀死了小鼠。在感染前3 ~ 6天,以1 ~ 100微克/只的浓度静脉注射m1Ado,增强效果最佳。另一方面,尿酸、尿嘧啶和假尿嘧啶没有表现出这种增强作用。腹腔注射植物血凝素后,m1Ado可抑制小鼠腹腔巨噬细胞的积累。虽然m1Ado在体外对巨噬细胞的吞噬和杀菌活性没有任何抑制作用,但提前3天接受m1Ado的小鼠腹腔巨噬细胞的杀菌活性显示出受损,这表明不同细胞群从m1Ado小鼠骨髓中迁移。结果可能表明m1Ado是肿瘤腹水的主要因素,在小剂量下,巨噬细胞功能受损,可以在荷瘤宿主中检测到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low molecular weight immunosuppressive factors found in elevated amounts in cancer ascitic fluids of mice. 2. 1-Methyladenosine isolated from cancer ascitic fluids enhances Listeria infection in mice.

The low molecular weight fraction (mol wt less than 1,000) of Ehrlich cancer ascitic fluid has been known to enhance Listeria infection in mice. Chemical characterization of the entities in this fraction revealed four purine and pyrimidine analogues, i.e. uric acid, uracil, pseudouridine and 1-methyladenosine (m1Ado). When the effect of each of these components was studied on Listeria infection in mice, only m1Ado markedly enhanced the infection and killed the mice within a short period. The optimal enhancement was obtained when m1Ado was given intravenously to mice 3-6 days before the infection at a concentration of between 1 and 100 micrograms/mouse. On the other hand, uric acid, uracil and pseudouridine failed to show such an enhancing effect. m1Ado inhibited macrophage accumulation in the peritoneal cavity of mice after an intraperitoneal injection of phytohemagglutinin. Although m1Ado did not show any inhibitory effect on the phagocytic and bactericidal activities of macrophages in vitro, peritoneal macrophages obtained from mice which received m1Ado 3 days ahead revealed impaired bactericidal activity, suggesting the migration of different cell populations from the bone marrow of m1Ado-receiving mice. The results may suggest that m1Ado is a major factor in tumor ascites causing, in small doses, an impairment of macrophage functioning as can be detected in tumor-bearing hosts.

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