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首页> 外文期刊>International Journal of Nanomedicine >Gold nanoparticle uptake is enhanced by estradiol in MCF-7 breast cancer cells
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Gold nanoparticle uptake is enhanced by estradiol in MCF-7 breast cancer cells

机译:雌二醇可促进MCF-7乳腺癌细胞吸收金纳米颗粒

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Purpose: In the present study, we investigated the effects of 17β-estradiol (Esub2/sub) on membrane roughness and gold nanoparticle (AuNP) uptake in MCF-7 breast cancer cells. Methods: Estrogen receptor (ER)-positive breast cancer cells (MCF-7) were exposed to bare 20?nm AuNPs in the presence and absence of 1×10sup?9/sup?M Esub2/sub for different time intervals for up to 24?hrs. The effects of AuNP incorporation and Esub2/sub incubation on the MCF-7 cell surface roughness were measured using atomic force microscopy (AFM). Endocytic vesicle formation was studied using confocal laser scanning microscopy (CLSM). Finally, the results were confirmed by hyperspectral optical microscopy. Results: High-resolution AFM images of the surfaces of MCF-7 membranes (up to 250 nmsup2/sup) were obtained. The incubation of cells for 12?hrs with AuNP and Esub2/sub increased the cell membrane roughness by 95% and 30% compared with the groups treated with vehicle (ethanol) or AuNPs only, respectively. This effect was blocked by an ER antagonist (7α,17β-[9-[(4,4,5,5,5-Pentafluoropentyl)sulfinyl]nonyl]estra-1,3,5(10)-triene-3,17-diol [ICI] 182,780). Higher amounts of AuNPs were localized inside MCF-7 cells around the nucleus, even after 6?hrs of Esub2/sub incubation, compared with vehicle-treated cells. Endolysosome formation was induced by Esub2/sub, which may be associated with an increase in AuNP-uptake. Conclusions: Esub2/sub enhances AuNP incorporation in MCF-7 cells by modulating of plasma membrane roughness and inducing lysosomal endocytosis. These findings provide new insights into combined nanotherapies and hormone therapies for breast cancer.
机译:目的:在本研究中,我们研究了17β-雌二醇(E 2 )对MCF-7乳腺癌细胞膜粗糙度和金纳米颗粒(AuNP)摄取的影响。方法:在存在和不存在1×10 ?9 ?ME 2 <的情况下,将雌激素受体(ER)阳性乳腺癌细胞(MCF-7)暴露于裸露的20nm nm AuNPs。 / sub>的不同时间间隔长达24小时。使用原子力显微镜(AFM)测量了AuNP掺入和E 2 孵育对MCF-7细胞表面粗糙度的影响。使用共聚焦激光扫描显微镜(CLSM)研究了内吞囊泡的形成。最后,通过高光谱光学显微镜证实了结果。结果:获得了MCF-7膜表面(最大250 nm 2 )的高分辨率AFM图像。与仅用赋形剂(乙醇)或AuNP处理的组相比,分别用AuNP和E 2 孵育细胞12小时可使细胞膜粗糙度分别提高95%和30%。该作用被ER拮抗剂(7α,17β-[9-[(4,4,5,5,5-五氟戊基)亚磺酰基]壬基]雌-1,3,5(10)-三烯-3,17阻滞-二醇[ICI] 182,780)。与媒介物处理过的细胞相比,即使在E 2 孵育6小时后,更高数量的AuNP也位于细胞核周围的MCF-7细胞内。 E 2 诱导了溶酶体的形成,这可能与AuNP的摄取增加有关。结论:E 2 通过调节质膜粗糙度并诱导溶酶体内吞作用增强MCF-7细胞中AuNP的掺入。这些发现为乳腺癌的纳米疗法和激素疗法的结合提供了新的见解。

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