Sokolova E P, Demidova G V, Ziuzina V P, Alekseeva L P, Bespalova I A, Tynianova V I
Zh Mikrobiol Epidemiol Immunobiol. 2010 Jul-Aug(4):59-64.
AIM. To study dynamics of synthesis of TNF-alpha and INF-gamma by cell line U-937 human monocytes under the effect of Yersinia pestis EV 76 lypopolysaccharides (LPS) with different levels of toxicity: original LPS28 and LPS37 as well as their conformationally--changed variants with enhanced toxicity--complex of LPS with murine toxin (MT) of Y. pestis, and LPS modified by biologicall active compound (BAC) obtained from human erythrocytes.
Using phenol method, LPS were obtained from Y. pestis EV 76 cells grown at 28 and 37 degrees C. Production of cytokines was measured by ELISA.
It was shown that original and modified forms of LPS28 and LPS37 induce synthesis of both TNF-alpha and INF-gamma by human monocytes. Expression of genes for two ways of synthesis of these cytokines points to activation and transmission of signal induced by all studied forms of Y. pestis EV 76 LPS through TLR4. Levels of activity of MyD88-dependent and MyD88-independent signaling pathways are different and depend from chemical structure of LPS28 and LPS37, conformation of their modified forms and duration of their exposition with monocytes. Dynamics ofcytokine synthesis corresponds to response of synergized TLR on activation with profound agonistic/antagonistic effect.
It was determined that conformational modifications of Y. pestis EV76 LPS occurring due to effect of MT and BAC accompanied by quantitative, qualitative and temporal changes of TNF-alpha and INF-gamma synthesis by human monocytes and correlate with increase of their toxic properties.
目的。研究不同毒性水平的鼠疫耶尔森菌EV 76脂多糖(LPS)对人单核细胞系U-937合成肿瘤坏死因子-α(TNF-α)和干扰素-γ(INF-γ)的影响:原始的LPS28和LPS37以及它们毒性增强的构象改变变体——LPS与鼠疫耶尔森菌鼠毒素(MT)的复合物,以及由人红细胞获得的生物活性化合物(BAC)修饰的LPS。
采用苯酚法从在28℃和37℃培养的鼠疫耶尔森菌EV 76细胞中获得LPS。通过酶联免疫吸附测定法(ELISA)检测细胞因子的产生。
结果表明,LPS28和LPS37的原始形式和修饰形式均可诱导人单核细胞合成TNF-α和INF-γ。这两种细胞因子合成途径的基因表达表明,所有研究的鼠疫耶尔森菌EV 76 LPS形式通过Toll样受体4(TLR4)诱导的信号激活和传递。髓样分化因子88(MyD88)依赖性和MyD88非依赖性信号通路的活性水平不同,且取决于LPS28和LPS37的化学结构、其修饰形式的构象以及它们与单核细胞接触的持续时间。细胞因子合成动力学对应于协同TLR对激活的反应,具有显著的激动/拮抗作用。
确定由于MT和BAC的作用,鼠疫耶尔森菌EV76 LPS的构象修饰伴随着人单核细胞合成TNF-α和INF-γ的数量、质量和时间变化,并与其毒性增加相关。