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Construction of novel in vitro epithelioid cell granuloma model from mouse macrophage cell line.

机译:从小鼠巨噬细胞系建立新型体外上皮样细胞肉芽肿模型。

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There have been several attempts to make granuloma model to clarify the mechanism of granulomatous diseases like sarcoidosis. However, a unique in vitro model that generates multinucleated giant cell (MGC) through epithelioid cells resembled to human granuloma, has not yet been clearly established. In this study, the generation of granuloma model that forms MGC via epithelioid cells from the mouse macrophage cell line was investigated. A RAW 246.7 mouse macrophage cell line was cultured with lipopolysaccharide (LPS) and concanavalin A (Con A) in various concentrations either alone or both. We found that separate treatment of LPS and Con A induced around 35 and 20% MGC respectively whereas cotreatment of these chemicals drastically accelerated granuloma formation rate and it was around 80%. The highest fusion index (MGC formation rate) was observed at days 7. A gradual increase of tumor necrosis factor alpha (TNF-alpha) production in the culture supernatant was analyzed by enzyme-linked immunosorbent assay (ELISA). And the neutralization of the elevated level of TNF-alpha production by its monoclonal antibody leads to significant decrease of MGC formation. Interestingly, we found that the RAW cells were changed into spindle cells, which morphologically resembled to epithelioid cells and eventually MGC was formed from these spindle cells. Our in vitro granuloma model appeared to be similar with in vivo epithelioid cell granulomas like sarcoidosis. Thus, our model would be useful as in vitro epithelioid granuloma model for analyzing the mechanisms and screening the effective drugs of granulomatous diseases in future.
机译:已经进行了一些尝试来建立肉芽肿模型以阐明肉芽肿病如结节病的机制。然而,尚未明确建立通过类似于人肉芽肿的上皮样细胞产生多核巨细胞(MGC)的独特体外模型。在这项研究中,研究了从小鼠巨噬细胞系通过上皮样细胞形成MGC的肉芽肿模型的产生。将RAW 246.7小鼠巨噬细胞细胞系与脂多糖(LPS)和伴刀豆球蛋白A(Con A)单独或以两种浓度培养。我们发现,LPS和Con A的单独处理分别诱导了约35%和20%的MGC,而这些化学药品的共处理极大地加速了肉芽肿的形成率,约为80%。在第7天观察到最高融合指数(MGC形成速率)。通过酶联免疫吸附测定(ELISA)分析了培养上清液中肿瘤坏死因子α(TNF-α)产生的逐渐增加。而且其单克隆抗体对TNF-α产生水平升高的中和作用导致MGC形成的显着减少。有趣的是,我们发现RAW细胞变成了纺锤体细胞,形态上类似于上皮样细胞,最终由这些纺锤体细胞形成了MGC。我们的体外肉芽肿模型似乎与体内上皮样细胞肉芽肿(如结节病)相似。因此,我们的模型可作为体外上皮样肉芽肿模型,用于今后分析肉芽肿性疾病的机理和筛选有效药物。

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