人类自然杀伤细胞衍生的纳米魔法子弹对急性髓性白血病(AML)的抗白血病活性

Zahra Kashani Khatib, Asma Maleki, A. Pourfatollah, A. Hamidieh, Shirin Ferdowsi
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摘要

背景:癌症是医学界严重的健康问题之一,在治疗方面,人们采用了严厉的治疗方法。然而,癌症患者的预后仍然很差。应用 NK 细胞衍生的外泌体(NK-Exo)是癌症免疫疗法的一种新方法。这种纳米颗粒的尺寸范围为 30-120 纳米,是一种小型的母细胞模型。本研究在体外研究了NK-Exo和LAK-Exo(活化的NK细胞衍生外泌体)对急性髓性白血病(AML)的抗肿瘤活性。材料与方法:采用MACS方法从健康供体的水包衣中分离NK细胞,并使用EXOCIBE试剂盒分离NK-Exo。用不同剂量的 NK-Exo 处理 KG-1 细胞系后,分别用 MTT 检测和附件素 V-PE 评估细胞增殖和凋亡情况,并用 Real-Time PCR 和 Western 印迹法确认相关蛋白。结果NK-Exo和LAK-Exo的抗肿瘤活性呈剂量和时间依赖性。与 50 µg/ml 外泌体培养 48 小时后,它们的活性最高(p<0.0001)。然而,低浓度的NK-Exo(p<0.05)和LAK-Exo(p<0.001)也能在短时间内显示出这种细胞毒性活性。不同途径诱导细胞凋亡与时间点有关。肿瘤细胞与50µg/ml NK-Exo和LAK-Exo共培养48小时后,凋亡率分别为34.56%和51.6%。在使用 50 µg/ml NK-Exo 和 LAK-Exo 处理的细胞中观察到 CASPASE3、P38 和 CYTOCHROME C 基因的显著表达。结论我们的研究证实了 NK-Exo 在体外对 AML 肿瘤细胞的抗白血病活性。因此,NK-Exo 可被视为一种治疗白血病的有效方法。
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Antileukemia Activity of Human Natural Killer Cell-Derived Nanomagic Bullets against Acute Myeloid Leukemia (AML)
Background: Cancer is among the serious health problems of the medical world, for treatment of which severe treatments are used. However, the prognosis of cancer patients is still poor. The application of NK cell-derived exosomes (NK-Exo) is a new method for cancer immunotherapy. These nanoparticles with a size range of 30-120 nm are a small model of mother cells. In this study, the anti-tumor activity of NK-Exo and LAK-Exo (activated NK cell-derived exosome) against acute myeloid leukemia (AML) is investigated in vitro. Materials and Methods: The MACS method was performed for the separation of NK cells from the buffy coats of healthy donors, and an EXOCIBE kit was used for the isolation of NK-Exo. After treating the KG-1 cell line with different doses of NK-Exo, MTT assay, and annexin V-PE were done to evaluate cell proliferation and apoptosis, respectively, and for confirmation of involved proteins, Real-Time PCR and western blotting were performed. Results: Anti-tumor activity of NK-Exo and LAK-Exo was dose- and time-dependent. Their highest activities were observed following 48 hours of incubation with 50 µg/ml exosome (p<0.0001). However, this cytotoxic activity was also seen over a short period of time with low concentrations of NK-Exo (p<0.05) and LAK-Exo (p<0.001).The cytotoxic effect of LAK-Exo on target cells was significantly higher than NK-EXO. The induction of apoptosis by different pathways was time-point dependent. Total apoptosis was 34.56% and 51.6% after 48 hours of tumor cell coculture with 50µg/ml NK-Exo and LAK-Exo, respectively. Significant expression of CASPASE3, P38, and CYTOCHROME C genes was observed in the cells treated with 50 µg/ml NK-Exo and LAK-Exo. Conclusion: Our study confirmed the antileukemia activity of NK-Exo against AML tumor cells in vitro. Therefore, NK-Exo can be considered as a promising and effective treatment for leukemia therapy.
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