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分枝杆菌索状因子海藻糖-6,6'-二霉菌酸诱导肺肉芽肿形成和消散过程中的细胞因子信息及蛋白表达

Cytokine message and protein expression during lung granuloma formation and resolution induced by the mycobacterial cord factor trehalose-6,6'-dimycolate.

作者信息

Perez R L, Roman J, Roser S, Little C, Olsen M, Indrigo J, Hunter R L, Actor J K

机构信息

Department of Medicine, Atlanta Veterans Affairs Medical Center, Emory University School of Medicine, Atlanta, GA 30033, USA.

出版信息

J Interferon Cytokine Res. 2000 Sep;20(9):795-804. doi: 10.1089/10799900050151067.

Abstract

Trehalose-6,6'-dimycolate (TDM), or cord factor, is a mycobacterial cell wall component that induces granuloma formation and proinflammatory cytokine production in vivo and in vitro. The purpose of this work was to better understand the mechanisms by which TDM promotes lung granuloma formation. This was accomplished by characterizing cytokine mRNA expression during TDM-induced alveolitis culminating in cohesive granuloma development. A single intravenous injection of TDM given to C57BL/6 mice produced lung granulomas that peaked in number 5 days after challenge and were nearly resolved by 14 days. mRNA in whole lung preparations was quantitated by bioluminescent RT-PCR. Tumor necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), and IL-6 were significantly elevated during granuloma development and decreased during granuloma resolution. There were no detectable changes in mRNA for interferon-y (IFN-y), IL-2, IL-4, IL-5, IL-10, and IL-12(p40). The level of TNF-alpha protein extracted from lung minces highly correlated with morphologic indices of granulomatous inflammation, indicating that it may be an important modulator of the inflammatory intensity induced by TDM. TDM may interact specifically with macrophages in vivo, as evidenced by induction of TNF-alpha, IL-1beta, and IL-6, but not IFN-gamma, protein in bone marrow-derived macrophages from C57BL/6 mice. TDM may therefore play an important role early in macrophage activation during the host granulomatous response to mycobacteria.

摘要

海藻糖-6,6'-二甲酯(TDM),即索状因子,是一种分枝杆菌细胞壁成分,可在体内和体外诱导肉芽肿形成及促炎细胞因子产生。本研究的目的是更好地了解TDM促进肺部肉芽肿形成的机制。这是通过在TDM诱导的肺泡炎最终导致紧密肉芽肿形成的过程中,对细胞因子mRNA表达进行表征来实现的。给C57BL/6小鼠单次静脉注射TDM后可产生肺部肉芽肿,其数量在攻击后5天达到峰值,并在14天时几乎消退。通过生物发光RT-PCR对全肺组织中的mRNA进行定量。在肉芽肿形成过程中,肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和IL-6显著升高,而在肉芽肿消退过程中则下降。干扰素-γ(IFN-γ)、IL-2、IL-4、IL-5、IL-10和IL-12(p40)的mRNA没有可检测到的变化。从肺组织匀浆中提取的TNF-α蛋白水平与肉芽肿性炎症的形态学指标高度相关,表明它可能是TDM诱导的炎症强度的重要调节因子。TDM可能在体内与巨噬细胞特异性相互作用,这一点从C57BL/6小鼠骨髓来源的巨噬细胞中TNF-α、IL-1β和IL-6而非IFN-γ蛋白的诱导可以证明。因此,TDM可能在宿主对分枝杆菌的肉芽肿反应中巨噬细胞激活的早期发挥重要作用。

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