Department of Stem Cell and Regenerative Biotechnology, Konkuk University, Seoul 05029, Korea.
Int J Nanomedicine. 2021 Jan 22;16:515-538. doi: 10.2147/IJN.S291138. eCollection 2021.
Several studies have demonstrated various molecular mechanisms involved in the biogenesis and release of exosomes. However, how external stimuli, such as platinum nanoparticles (PtNPs), induces the biogenesis and release of exosomes remains unclear. To address this, PtNPs were synthesized using lutein to examine their effect on the biogenesis and release of exosomes in human lung epithelial adenocarcinoma cancer cells (A549).
The size and concentration of isolated exosomes were characterized by dynamic light scattering (DLS) and nanoparticle tracking analysis system (NTA). Morphology and structure of exosomes were examined using scanning electron microscopy and transmission electron microscopy (TEM), respectively. Quantification of exosomes were analyzed by EXOCET assay and fluorescence polarization (FP). The expression of typical markers of exosomes were analyzed by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and enzyme-linked immunosorbent assay (ELISA).
A549 cells cultured with PtNPs enhance exosome secretion by altering various physiological processes. Interestingly, A549 cells treated with PtNPs increases total protein concentration, biogenesis and release of exosomes associated with PtNPs-induced oxidative stress. GW4869 inhibits PtNPs induced biogenesis and release of exosomes and also acetylcholinesterase (AChE), neutral sphingomyelinase activity (n-SMase), and exosome counts. A549 cells pre-treated with N-acetylcysteine (NAC) significantly inhibited PtNPs induced exosome biogenesis and release. These findings confirmed that PtNPs-induced exosome release was due to the induction of oxidative stress and the ceramide pathway. These factors enhanced exosome biogenesis and release and may be useful in understanding the mechanism of exosome formation, release, and function.
PtNPs provide a promising agent to increase exosome production in A549 cells. These findings offer novel strategies for enhancing exosome release, which can be applied in the treatment and prevention of cancer. Importantly, this is the first study, to our knowledge, showing that PtNPs stimulate exosome biogenesis by inducing oxidative stress and the ceramide pathway.
多项研究已经证明了参与外泌体生物发生和释放的各种分子机制。然而,外部刺激(如铂纳米颗粒(PtNPs))如何诱导外泌体的生物发生和释放尚不清楚。为了解决这个问题,使用叶黄素合成了 PtNPs,以研究它们对人肺上皮腺癌细胞(A549)中外泌体生物发生和释放的影响。
通过动态光散射(DLS)和纳米颗粒跟踪分析系统(NTA)对分离的外泌体的大小和浓度进行了表征。使用扫描电子显微镜和透射电子显微镜(TEM)分别检查了外泌体的形态和结构。通过 EXOCET 测定和荧光偏振(FP)分析了外泌体的定量。通过定量逆转录聚合酶链反应(qRT-PCR)和酶联免疫吸附测定(ELISA)分析了外泌体的典型标志物的表达。
用 PtNPs 培养的 A549 细胞通过改变各种生理过程增强了外泌体的分泌。有趣的是,用 PtNPs 处理的 A549 细胞增加了与 PtNPs 诱导的氧化应激相关的总蛋白浓度、外泌体的生物发生和释放。GW4869 抑制了 PtNPs 诱导的外泌体生物发生和释放,以及乙酰胆碱酯酶(AChE)、中性鞘磷脂酶活性(n-SMase)和外泌体计数。用 N-乙酰半胱氨酸(NAC)预处理的 A549 细胞显著抑制了 PtNPs 诱导的外泌体生物发生和释放。这些发现证实,PtNPs 诱导的外泌体释放是由于诱导了氧化应激和神经酰胺途径。这些因素增强了外泌体的生物发生和释放,可能有助于理解外泌体形成、释放和功能的机制。
PtNPs 为增加 A549 细胞中外泌体的产生提供了一种有前途的试剂。这些发现为增强外泌体的释放提供了新的策略,可应用于癌症的治疗和预防。重要的是,据我们所知,这是第一项研究表明,PtNPs 通过诱导氧化应激和神经酰胺途径刺激外泌体的生物发生。