自然杀伤细胞衍生的外泌体模拟物作为甲状腺癌细胞体外化疗药物的天然纳米载体。

L Zhu, B-C Ahn
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引用次数: 0

摘要

背景:外泌体已经成为纳米技术治疗和识别许多疾病的潜在领域。然而,外泌体的产生是一个困难、耗时和低产量的过程。同时,外泌体模拟物(exosome mimetics, EM)在特性上与外泌体相似,但产量更高。本研究的目的是制备负载索拉非尼的NK细胞源性EM (NKEM),并测试其对甲状腺癌细胞的杀伤能力。材料和方法:在NKEM生产过程中,将索拉非尼与NK细胞混合,将索拉非尼装入NKEM (NKEM- s)。然后,利用纳米颗粒跟踪分析(NTA)对这两种类型的纳米颗粒进行了表征,测量了它们的尺寸。此外,利用激光共聚焦显微镜和生物发光成像(BLI)技术研究了nkems对甲状腺癌细胞的细胞摄取和体外杀伤作用。结果:观察到甲状腺癌细胞对NKEM和NKEM- s的摄取。此外,BLI证实了nkems对两种甲状腺癌细胞的杀伤和抗增殖作用。尤其重要的是,NKEM-S甚至对间变性甲状腺癌(ATC)细胞也有良好的杀伤作用。结论:负载索拉非尼的NKEM具有体外杀伤甲状腺癌细胞的能力,甚至可以对抗ATC。这为药物输送系统和甲状腺癌治疗提供了新的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural Killer Cell-Derived Exosome Mimetics as Natural Nanocarriers for In Vitro Delivery of Chemotherapeutics to Thyroid Cancer Cells.

Background: Exosomes have become a potential field of nanotechnology for the treatment and identification of many disorders. However, the generation of exosomes is a difficult, time-consuming, and low-yielding procedure. At the same time, exosome mimetics (EM) resemble exosomes in their characteristics but have higher production yields. The aim of this study was to produce natural killer (NK) cell-derived EM (NKEM) loaded with sorafenib and test their killing ability against thyroid cancer cell lines.

Materials and methods: Sorafenib was loaded into NKEM by mixing sorafenib with NK cells during NKEM production (NKEM-S). Then, these two types of nanoparticles were characterized with nanoparticle tracking analysis (NTA) to measure their sizes. In addition, the cellular uptake and in vitro killing effect of NKEM-S on thyroid cancer cell lines were investigated using confocal laser microscopy and bioluminescence imaging (BLI) techniques.

Results: The uptake of NKEM and NKEM-S by the thyroid cancer cells was observed. Moreover, BLI confirmed the killing and anti-proliferation effect of NKEM-S on two thyroid cancer cell lines. Especially important, the NKEM-S demonstrated a desirable killing effect even for anaplastic thyroid cancer (ATC) cells.

Conclusion: Sorafenib-loaded NKEM showed the ability to kill thyroid cancer cells in vitro, even against ATC. This provides a new opportunity for drug delivery systems and thyroid cancer treatment.

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