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Induced cell toxicity originates dendritic cell death following magnetic hyperthermia treatment

机译:磁热治疗后,诱导的细胞毒性导致树突状细胞死亡

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Magnetic hyperthermia (MH) is based on the use of magnetic nanoparticles (MNPs) to selectively increase the temperature of MNP-loaded target tissues when applying an alternating magnetic field (AMF) in the range of radiofrequency. To date, all MH research has focused on heat generation in an attempt to elucidate the mechanisms for the death of MNP-loaded cells submitted to AMF. However, recent in vitro studies have demonstrated the feasibility of inducing dramatic cell death without increasing the macroscopic temperature during AMF exposure. Here, we show that the cell death observed following AMF exposure, specifically that of MNP-loaded dendritic cells (DCs) in culture, was caused by the release of toxic agents into the cell culture supernatants and not due to a macroscopic temperature increase. We performed MH in vitro experiments to demonstrate that the supernatant of the cell culture following AMF exposure was highly toxic when added to control unloaded DCs, as this treatment led to nearly 100% cell death. Therefore, our results demonstrate that heat is not the only agent responsible for triggering cell death following MH treatment. This finding offers new perspectives for the use of DCs as the proverbial Trojan horse to vectorise MNPs to the target tumour area and these results further support the use of DCs as therapeutic agents against cancer when submitted to AMF. Furthermore, this discovery may help in understanding the mechanism of cell death mediated by exposure to AMF.
机译:磁热疗(MH)是基于在施加射频范围内的交变磁场(AMF)时使用磁性纳米颗粒(MNP)来选择性地提高MNP加载的目标组织的温度。迄今为止,所有MH研究都集中在热量产生上,以阐明提交AMF的MNP加载细胞死亡的机制。但是,最近的体外研究证明了在不增加AMF暴露期间宏观温度的情况下诱导细胞死亡的可行性。在这里,我们表明,在AMF暴露后观察到的细胞死亡,特别是在培养物中装载MNP的树突状细胞(DC)的死亡是由有毒物质释放到细胞培养上清液中引起的,而不是宏观温度升高引起的。我们进行了MH体外实验,以证明AMF暴露后细胞培养上清液添加到对照空载DC中时具有剧毒,因为这种处理导致近100%的细胞死亡。因此,我们的结果表明,加热不是MH治疗后引发细胞死亡的唯一媒介。这一发现为使用DC作为众所周知的特洛伊木马为将MNP矢量化到目标肿瘤区域提供了新的视角,这些结果进一步支持了DC在提交AMF时作为抗癌治疗剂的使用。此外,这一发现可能有助于理解暴露于AMF介导的细胞死亡机制。

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