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病毒感染的细胞培养物产生巨噬细胞移动抑制因子。

Production of macrophage migration inhibition factors by virus-infected cell cultures.

作者信息

Flanagan T D, Yoshida T, Cohen S

出版信息

Infect Immun. 1973 Aug;8(2):145-50. doi: 10.1128/iai.8.2.145-150.1973.

Abstract

Macrophage migration inhibitory (MIF-like) activity was demonstrated in the supernatant fluids from cultures of African green monkey kidney cells (BGM) infected with mumps virus or Newcastle disease virus. We could detect no such activity in noninfected cultures. The virus-induced activity reported here is not due to nonspecific cytotoxic material released by dead or dying cells, and it does not require cell replication for its production. Preliminary estimates of molecular weight by Sephadex G-100 chromatography revealed a broad band of activity associated with the 45,000 and 65,000 markers. These are significantly smaller than previously reported chemotactic substances from virus-infected cultures, and thus appear to represent different cell products. These MIF-like factors may be produced concomitantly with interferon. However, ultraviolet irradiation of appropriate duration abolishes the ability of viruses to induce substances with MIF-like activity while preserving the ability to induce interferon. This strongly suggests that interferon is not the agent responsible for the macrophage migration inhibition effect. The functional properties of these various cell products induced by virus infection suggest that they all may play a role in the response to virus infection in vivo.

摘要

在感染腮腺炎病毒或新城疫病毒的非洲绿猴肾细胞(BGM)培养物的上清液中,证实了巨噬细胞迁移抑制(类MIF)活性。在未感染的培养物中,我们未检测到此类活性。此处报道的病毒诱导活性并非源于死亡或濒死细胞释放的非特异性细胞毒性物质,其产生也不需要细胞复制。通过葡聚糖G - 100色谱法对分子量进行的初步估计显示,有一条宽活性带与45,000和65,000标记物相关。这些明显小于先前报道的来自病毒感染培养物的趋化物质,因此似乎代表不同的细胞产物。这些类MIF因子可能与干扰素同时产生。然而,适当时长的紫外线照射消除了病毒诱导具有类MIF活性物质的能力,同时保留了诱导干扰素的能力。这有力地表明,干扰素并非负责巨噬细胞迁移抑制作用的因子。病毒感染诱导的这些各种细胞产物的功能特性表明,它们都可能在体内对病毒感染的反应中发挥作用。

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Interferon preparations enhance phagocytosis in vivo.干扰素制剂可增强体内的吞噬作用。
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