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Effects of combined delivery of extremely low frequency electromagnetic field and magnetic Fe3O4 nanoparticles on hepatic cell lines

机译:极低频电磁场和磁性Fe3O4纳米粒子联合递送对肝细胞系的影响

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摘要

Magnetic Fe3O4 nanoparticles (MNPs) have shown promise as drug carriers for treating lung and liver tumors in vivo. However, little is known about the combined delivery of these MNPs with a second approach, extremely low frequency electro-magnetic field (ELFF) exposure, which has been shown to have value for in vitro treatment of tumor cells. Here, ELFF and MNPs were combined to treat healthy (HL-7702) and cancerous (Bel-7402, HepG2) hepatic cells lines to explore the potential therapeutic effects, bio-mechanisms, and potential toxicity of a combined drug-free treatment in vitro. Flow cytometry for anti-AFP (alpha fetal protein) antibody, which coated the MNPs, indicated that the combined treatment induced Bel-7402 and HepG2 hepatoma cells lines into early apoptosis, without significant effects on healthy hepatic cells. This effect appeared to be mediated through cellular membrane ion metabolism. The presence of AFP-loaded MNPs strengthened the effects of ELFF on tumor cells, inducing a higher frequency of early apoptosis, while having minimal toxic effects on healthy HL-7702 cells. Western blotting revealed that the apoptosis-triggering BCL proteins were up regulated in hepatoma cells compared to healthy cells. Flow cytometry and patch-clamp studies revealed that this resulted from a higher MNP uptake ratio and greater cellular membrane ion exchange current in tumor cells compared to HL-7702 cells. Further, patch-clamp results showed that combining MNPs with ELFF treatment induces cells into early apoptosis through an ion metabolism disturbance in cells, similar to ELFF treatment. In brief, the combination of ELFF and MNPs had beneficial effects on tumor cells without significant toxicity on healthy cells, and these effects were associated with cellular MNP uptake.
机译:磁性Fe3O4纳米颗粒(MNP)已显示出有望作为体内治疗肺和肝肿瘤的药物载体。但是,关于这些MNP与第二种方法(极低频电磁场(ELFF)暴露)的联合递送知之甚少,这已被证明对体外治疗肿瘤细胞具有价值。在这里,ELFF和MNPs结合起来治疗健康的(HL-7702)和癌性的(Bel-7402,HepG2)肝细胞系,以探索无药联合体外治疗的潜在治疗效果,生物机制和潜在毒性。覆盖MNP的抗AFP(α胎儿蛋白)抗体的流式细胞术表明,联合治疗可诱导Bel-7402和HepG2肝癌细胞系进入早期凋亡状态,而对健康的肝细胞无明显影响。这种作用似乎是通过细胞膜离子代谢介导的。载有AFP的MNP的存在增强了ELFF对肿瘤细胞的作用,诱导了较高的早期凋亡频率,而对健康的HL-7702细胞的毒性却很小。 Western印迹显示,与健康细胞相比,肝癌细胞中触发凋亡的BCL蛋白被上调。流式细胞仪和膜片钳研究表明,这是由于与HL-7702细胞相比,肿瘤细胞中更高的MNP吸收率和更大的细胞膜离子交换电流所致。此外,膜片钳结果显示,与ELFF处理类似,将MNP与ELFF处理组合可通过细胞中的离子代谢紊乱诱导细胞进入早期凋亡。简而言之,ELFF和MNP的组合对肿瘤细胞具有有益的作用,而对健康细胞没有明显的毒性,并且这些作用与细胞对MNP的摄取有关。

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