超极化13C核磁共振纵向细胞内代谢使用移动3D细胞培养系统

T.B.W. Mathiassen , A.E. Høgh , M. Karlsson , S. Katsikis , K. Wang , M. Pennestri , J.H. Ardenkjær-Larsen , P.R. Jensen
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引用次数: 0

摘要

超极化与溶解动态核极化(dDNP)技术产生>核磁共振活性核(如13C)信号增加10000倍。因此,超极化13c标记的代谢示踪剂分子可以在没有干扰背景的情况下实时观察活细胞系统中的生化途径。这种方法适用于直接观察药物治疗、感染或其他疾病引起的细胞内化学反应的改变。利用核磁共振和dDNP-NMR对哺乳动物细胞进行纵向细胞研究时,一个反复出现的挑战是在核磁共振波谱仪中保持细胞活力。3D细胞培养方法越来越受欢迎,因为与2D细胞培养相比,它们提供了更相关的生理环境。基于这些策略,设计了一个移动三维文化系统。使用临床药物依托泊苷治疗癌细胞(HeLa),并使用超极化[1-13C]丙酮酸测定由此产生的代谢改变。我们表明,在细胞培养箱中维持细胞培养,仅将细胞转移到核磁共振波谱仪中进行dnp -NMR测量所需的几分钟,是核磁共振管中细胞维持的一个有吸引力的选择。维持高细胞活力,实验吞吐量翻了许多倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Hyperpolarized 13C NMR for longitudinal in-cell metabolism using a mobile 3D cell culture system

Hyperpolarization with the dissolution dynamic nuclear polarization (dDNP) technique yields > 10,000-fold signal increases for NMR-active nuclei (e.g. 13C). Hyperpolarized 13C-labeled metabolic tracer molecules thus allow real-time observations of biochemical pathways in living cellular systems without interfering background. This methodology lends itself to the direct observation of altered intracellular reaction chemistry imparted for instance by drug treatment, infections, or other diseases. A reoccurring challenge for longitudinal cell studies of mammalian cells with NMR and dDNP-NMR is maintaining cell viability in the NMR spectrometer. 3D cell culture methods are increasing in popularity because they provide a physiologically more relevant environment compared to 2D cell cultures. Based on such strategies a mobile 3D culture system was devised. The clinical drug etoposide was used to treat cancer cells (HeLa) and the resulting altered metabolism was measured using hyperpolarized [1–13C]pyruvate. We show that sustaining the cell cultivation in cell incubators and only transferring the cells to the NMR spectrometer for the few minutes required for the dDNP-NMR measurements is an attractive alternative to cell maintenance in the NMR tube. High cell viability is sustained, and experimental throughput is many doubled.

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