肿瘤坏死因子α
细胞因子
肺
巨噬细胞
肉芽肿
体内
促炎细胞因子
免疫学
炎症
病理
生物
体外
医学
内科学
生物化学
生物技术
作者
Rafael L. Perez,Jesse Roman,Susanne Roser,Candice Little,Margaret Olsen,Jessica Indrigo,Robert L. Hunter,Jeffrey K. Actor
出处
期刊:Journal of Interferon and Cytokine Research
[Mary Ann Liebert]
日期:2000-09-01
卷期号:20 (9): 795-804
被引量:91
标识
DOI:10.1089/10799900050151067
摘要
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-α (TNF-α), interleukin1β (IL-1β), and IL-6 were significantly elevated during granuloma development and decreased during granuloma resolution. There were no detectable changes in mRNA for interferon-γ (IFN-γ), IL-2, IL-4, IL-5, IL10, and IL-12(p40). The level of TNF-α 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-α, IL-1β, and IL-6, but not IFN-γ, 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.
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