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病毒诱导的干扰素制剂对巨噬细胞迁移的抑制作用。

Inhibition of macrophage migration by virus-induced interferon preparations.

作者信息

Imanishi J

出版信息

Jpn J Microbiol. 1975 Oct;19(5):337-42. doi: 10.1111/j.1348-0421.1975.tb00889.x.

DOI:10.1111/j.1348-0421.1975.tb00889.x
PMID:1241396
Abstract

It was found that a preparation of mouse L cell interferon induced by Newcastle disease virus (NDV) possessed not only interferon activity but also inhibitory activity upon migration of guinea pig peritoneal macrophages (MIF activity). These activities were also observed in a preparation of human leukocyte interferon induced by NDV. The interferon and MIF activities shared common characteristics in the dose response, time course of in vitro production, thermal stability, sensitivity to trypsin and periodate, and elution pattern in CM-Sephadex column chromatography. However, gel filtration pattern with Sephadex G-100 showed two separate peaks. Fractions collected from the first peak, corresponding to a molecular weight of about 45 000, had only the MIF activity, while those collected from the second peak, corresponding to a molecular weight of about 30 000, had both the interferon and MIF activities. A preparation of mouse brain interferon induced by Japanese encephalitis virus had a much weaker MIF activity than the L cell interferon, although these preparations were equal in interferon activity (5000 units/ml).

摘要

研究发现,新城疫病毒(NDV)诱导产生的小鼠L细胞干扰素制剂不仅具有干扰素活性,而且对豚鼠腹腔巨噬细胞的迁移具有抑制活性(MIF活性)。在NDV诱导产生的人白细胞干扰素制剂中也观察到了这些活性。干扰素和MIF活性在剂量反应、体外产生的时间进程、热稳定性、对胰蛋白酶和高碘酸盐的敏感性以及CM-葡聚糖凝胶柱色谱中的洗脱模式方面具有共同特征。然而,用葡聚糖凝胶G-100进行的凝胶过滤图谱显示有两个分开的峰。从第一个峰收集的级分,对应分子量约为45000,仅具有MIF活性,而从第二个峰收集的级分,对应分子量约为30000,同时具有干扰素和MIF活性。日本脑炎病毒诱导产生的小鼠脑干扰素制剂的MIF活性比L细胞干扰素弱得多,尽管这些制剂的干扰素活性相同(5000单位/毫升)。

相似文献

1
Inhibition of macrophage migration by virus-induced interferon preparations.病毒诱导的干扰素制剂对巨噬细胞迁移的抑制作用。
Jpn J Microbiol. 1975 Oct;19(5):337-42. doi: 10.1111/j.1348-0421.1975.tb00889.x.
2
Rabbit macrophage interferons. II. Some physicochemical properties and estimations of molecular weights.兔巨噬细胞干扰素。II. 一些物理化学性质及分子量测定
J Exp Med. 1967 Apr 1;125(4):579-93. doi: 10.1084/jem.125.4.579.
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Enhancement of bactericidal activity of mouse peritoneal macrophages against Staphylococcus aureus by mouse interferon preparations.
Biken J. 1982 Jun;25(2):71-7.
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Production and initial characterization of guinea pig interferon.豚鼠干扰素的制备及初步特性研究
J Interferon Res. 1980 Fall;1(1):19-22. doi: 10.1089/jir.1980.1.19.
5
Analysis of the interferons induced in mice in vivo and in macrophages in vitro by Newcastle disease virus and by polyinosinic-polycytidylic acid.新城疫病毒和聚肌苷酸-聚胞苷酸在体内诱导小鼠及体外诱导巨噬细胞产生干扰素的分析。
J Interferon Res. 1986 Feb;6(1):21-8. doi: 10.1089/jir.1986.6.21.
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Production of macrophage migration inhibition factors by virus-infected cell cultures.病毒感染的细胞培养物产生巨噬细胞移动抑制因子。
Infect Immun. 1973 Aug;8(2):145-50. doi: 10.1128/iai.8.2.145-150.1973.
7
Long-term culture of guinea pig tongue cells: a suitable interferon system.豚鼠舌细胞的长期培养:一种合适的干扰素系统。
Acta Virol. 1979 Mar;23(2):162-4.
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Phagocytosis-enhancing effect of human leukocyte interferon preparation of human peripheral monocytes in vitro.
Acta Virol. 1975 Jan;19(1):52-8.
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Partial purification of guinea pig MIF by affinity column chromatography using macrophages.使用巨噬细胞通过亲和柱色谱法对豚鼠巨噬细胞移动抑制因子进行部分纯化。
Microbiol Immunol. 1979;23(6):533-41. doi: 10.1111/j.1348-0421.1979.tb00492.x.
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Characterization of two distinct molecular populations of type I mouse interferons.I型小鼠干扰素两种不同分子群体的特征描述。
J Gen Virol. 1977 Nov;37(2):277-84. doi: 10.1099/0022-1317-37-2-277.

引用本文的文献

1
Advances in interferon research - Medical Staff Conference.干扰素研究进展——医务人员会议
West J Med. 1982 Mar;136(3):227-35.