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鼠类土拉菌病病程中产生的巨噬细胞激活因子:对微生物增殖的影响

Macrophage activating factors produced in the course of murine tularemia: effect on multiplication of microbes.

作者信息

Kovarova H, Marcela A, Stulik J

机构信息

Department of Biochemistry, Faculty of Medicine, Charles University, Hradec Kralove, Czecho-Slovakia.

出版信息

Arch Immunol Ther Exp (Warsz). 1992;40(3-4):183-90.

PMID:1300982
Abstract

Primary F. tularensis infection in mice induces the production of macrophage activating factors (MAFs) by spleen cells. The stimulation of macrophage cytolytic activity (MAF-c) and hydrogen peroxide production (MAF-H2O2) dominates between days 7 and 10 in the course of tularemia. Three various pools of active fractions (10-11, 14-15, 25-28) were fractionated by two-step chromatography. Typical for 10-11 and 14-15 is MAF-c activity whereas in 25-28 prevails MAF-H2O2. Initial concentrated supernatant (day 7 of infection) and individual fractions have been used to raise antibodies KI (anti 10-11) and KII (anti 14-15). Neutralization reactions with specific antibodies indicate the presence of tumor necrosis factor alpha (TNF alpha) in 14-15 (44% inhibitable), interferon gamma (IFN gamma) and interleukin 2 (IL 2) in 25-28 (65% and 30% neutralization, respectively). Utilizing KI and KII, 99% and 90% inhibition of cytolytic activity is reached in 10-11 and 14-15, respectively, in spite of non-specific cross reaction. Western blot analysis of proteins in supernatant on day 7 detects, besides TNF alpha, further protein bands (13, 15.5, 52 and 72 kDa) that seem to be associated with macrophage activation. Significant protective effect against in vivo multiplication of tularemic microbes indicates a certain role of TNF alpha, however, cooperation of other molecules is worth to be taken into consideration.

摘要

小鼠原发性土拉弗朗西斯菌感染可诱导脾细胞产生巨噬细胞激活因子(MAFs)。在兔热病病程的第7至10天,巨噬细胞溶细胞活性(MAF-c)和过氧化氢生成(MAF-H2O2)的刺激作用占主导。通过两步色谱法对三个不同的活性级分池(10 - 11、14 - 15、25 - 28)进行了分离。10 - 11和14 - 15的典型特征是MAF-c活性,而25 - 28中MAF-H2O2占优势。初始浓缩上清液(感染第7天)和各个级分已用于制备抗体KI(抗10 - 11)和KII(抗14 - 15)。与特异性抗体的中和反应表明,14 - 15中存在肿瘤坏死因子α(TNFα)(44%可被抑制),25 - 28中存在干扰素γ(IFNγ)和白细胞介素2(IL 2)(分别为65%和30%中和)。尽管存在非特异性交叉反应,但利用KI和KII分别在10 - 11和14 - 15中对溶细胞活性达到了99%和90%的抑制。对感染第7天上清液中蛋白质的蛋白质印迹分析除检测到TNFα外,还检测到其他蛋白条带(13、15.5、52和72 kDa),这些条带似乎与巨噬细胞激活有关。对兔热病微生物体内增殖具有显著的保护作用,这表明TNFα具有一定作用,然而,其他分子的协同作用也值得考虑。

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