聚乙烯亚胺
细胞因子
肿瘤坏死因子α
促炎细胞因子
免疫系统
分子生物学
生物
肺
干扰素
免疫学
体内
实时聚合酶链反应
转染
炎症
医学
基因
内科学
生物化学
生物技术
出处
期刊:Journal of Aerosol Medicine and Pulmonary Drug Delivery
[Mary Ann Liebert]
日期:2013-06-22
卷期号:27 (2): 117-124
被引量:1
标识
DOI:10.1089/jamp.2012.1003
摘要
Background: The expression of inflammatory cytokines in lung tissue plays an important role in immune function of the lung. In this study, we tested whether aerosol delivery of the gene of interferon-γ (IFNγ) could affect inflammatory cytokine expression in mouse lung. Methods: Murine IFNγ-expressing plasmids (pcDNA-IFNγ) complexed with polyethylenimine (PEI) (PEI/pcDNA-IFNγ) were constructed, and their transfection efficiency was assessed in vivo using real-time quantitative RT-PCR and enzyme-linked immunosorbent assay. After aerosol administration of the plasmid complexes and confirmation of the IFNγ plasmid location in lung tissue, we measured mRNA levels of the inflammatory cytokines interleukin-1 (IL-1), IL-6, IL-10, tumor necrosis factor-α (TNF-α), and granulocyte-macrophage colony-stimulating factor (GM-CSF) on days 1 to 7 in mouse lung tissues using real-time RT-PCR. Results: IFNγ mRNA expression in mouse lung was significantly increased 24 hr after a single aerosol administration of PEI/pcDNA-IFNγ and gradually decreased over the next 5 days, whereas the mRNA expressions of IL-1, IL-6, and GM-CSF were markedly decreased, but not those of IL-10 and TNF-α. Conclusions: PEI/IFNγ gene therapy delivered by aerosol has immune-regulating potential by suppressing lung cytokine mRNA expression, and therefore may alleviate lung disease.
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