首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Combined effect of silver nanoparticles and aluminium chloride, butylparaben or diethylphthalate on the malignancy of MDA-MB-231 breast cancer cells and tumor-specific immune responses of human macrophages and monocyte-derived dendritic cells
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Combined effect of silver nanoparticles and aluminium chloride, butylparaben or diethylphthalate on the malignancy of MDA-MB-231 breast cancer cells and tumor-specific immune responses of human macrophages and monocyte-derived dendritic cells

机译:银纳米粒子和氯化铝,丁基根或二乙醇酸盐对人巨噬细胞和单核细胞衍生树突细胞MDA-MB-231乳腺癌细胞恶性肿瘤的综合作用及肿瘤特异性免疫反应

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The aim of this study was to assess whether silver nanoparticles (AgNP) or selected cosmetic ingredients may modify functions of various immunocompetent cell populations. To this end, the effect of two AgNP (size of 15 nm or 45 nm), alone and in combination with aluminium chloride, butyl paraben, di-n-butyl phthalate or diethyl phthalate was assessed on: (1) migration and invasion of MDA-MB-231 human breast cancer cells; (2) M1/M2 polarization of phorbol 12-myristate 13-acetate (PMA)-differentiated THP-1 macrophages (MO) and (3) activation/maturation of monocyte-derived dendritic cells (DCs). The results of this study showed that neither any of the test chemicals alone nor the mixtures significantly changed the migration or invasion ability of MDAMB-231 cells following, both 72-h and 21-day exposure. Analysis of the expression of marker genes for both M1 (IL-1B, CXCL9, TNF) and M2 (DCSIGN, MRC1) polarization revealed that the chemicals/mixtures did not activate M1/M2 differentiation of the MO macrophages. In addition, no significant changes were observed in the expression of CD86, HLA-DR and CD54 surface markers and phagocytic activity of DCs following 48-h exposure to AgNP alone or in combination with test compounds.
机译:本研究的目的是评估银纳米颗粒(AGNP)或选择的化妆品成分是否可以改变各种免疫活性细胞群的函数。为此,评估两种AgNP(大小为15nm或45nm)的效果,单独和与氯化铝,酸叔丁酯,邻苯二甲酸二丁酯或邻苯二甲酸二丁酯或二乙二醇酯组合进行评估:(1)迁移和侵袭MDA-MB-231人乳腺癌细胞; (2)Phorbol 12-Myristerate的M1 / M2偏振偏振13-乙酸酯(PMA) - 异细胞化的THP-1巨噬细胞(MO)和(3)单核细胞衍生的树突细胞(DC)的活化/成熟。该研究的结果表明,单独的任何测试化学品也不明显改变MDAMB-231细胞的迁移或侵袭能力,均为72-H和21天暴露。分析M1(IL-1B,CXCL9,TNF)和M2(DCSIGN,MRC1)极化的标记基因的表达显示,化学品/混合物未激活MO巨噬细胞的M1 / M2分化。此外,在48-H暴露于单独的AgNP之后的CD86,HLA-DR和CD54表面标志物和DCs的吞噬活性的表达中没有观察到显着变化,或者与测试化合物组合。

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