首页> 外文期刊>The Journal of toxicological sciences >The effects of Phorbol 12-myristate 13-acetate concentration on the expression of miR-155 and miR-125b and their macrophage function-related genes in the U937 cell line
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The effects of Phorbol 12-myristate 13-acetate concentration on the expression of miR-155 and miR-125b and their macrophage function-related genes in the U937 cell line

机译:Phorbol 12-myristate 13-醋酸盐浓度对U937细胞系MiR-155和miR-125b表达及其巨噬细胞功能相关基因的影响

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The phorbol 12-myristate 13-acetate (PMA)-induced U937 cell line has been widely used as an in vitro model for studying the functions of human macrophages. However, there are several concentrations of PMA commonly used to drive the differentiation of monocytic cell line to macrophage. Also, the expression of microRNA-155 (miR-155) and miR-125b in PMA-treated human monocytic cell line has not yet been reported. The five usual concentrations of PMA for stimulating macrophage differentiation are 10, 25, 50, 100, and 200 nM. In this study we compared the expression levels of miR-155, miR-125b and their related genes involved in macrophage functions in U937-derived cells after treatment with those five concentrations. The morphological study results showed that the five concentrations of PMA could induce macrophage differentiation in a similar manner. Moreover, cell proliferation and viability were not significantly different among these five conditions excepted the lower cell viability at 200 nM of PMA treatment. The five concentrations of PMA could upregulate the expression of miR-155 and miR-125b and increase the phagocytic activity of U937-derived cells in dose-reversal manner. The upregulation of miR-155 was correlated with increased expression levels of TNF alpha and decreased expression levels of BACH1 and CEBP beta, while the reduction of IRF4 was correlated with increased expression levels of miR-125b. Our study found that PMA could stimulate macrophage differentiation in a broad range of concentrations, however, the lower concentration could upregulate the higher expression of both miR-155 and miR-125b, and that correlated with the phagocytic functional activity of U937-derived macrophages.
机译:佛波醇12肉豆蔻酸13醋酸盐(PMA)诱导的U937细胞系已被广泛用作研究人类巨噬细胞功能的体外模型。然而,有几种浓度的PMA通常用于驱动单核细胞系向巨噬细胞的分化。此外,在PMA处理的人单核细胞系中microRNA-155(miR-155)和miR-125b的表达尚未见报道。PMA刺激巨噬细胞分化的五种常用浓度分别为10、25、50、100和200 nM。在这项研究中,我们比较了经这五种浓度处理后,U937衍生细胞中miR-155、miR-125b及其参与巨噬细胞功能的相关基因的表达水平。形态学研究结果表明,五种浓度的PMA都能以相似的方式诱导巨噬细胞分化。此外,这五种情况下的细胞增殖和活力没有显著差异,但PMA处理的细胞活力在200 nM处较低。五种浓度的PMA均能上调miR-155和miR-125b的表达,并以剂量逆转的方式增加U937衍生细胞的吞噬活性。miR-155的上调与TNF-α的表达水平升高、BACH1和CEBP-β的表达水平降低相关,而IRF4的降低与miR-125b的表达水平升高相关。我们的研究发现,PMA可以在广泛的浓度范围内刺激巨噬细胞分化,然而,较低浓度可以上调miR-155和miR-125b的高表达,并且与U937衍生巨噬细胞的吞噬功能活性相关。

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