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Real-time quantitative analysis of metabolic flux in live cells using a hyperpolarized micromagnetic resonance spectrometer

机译:使用超极化微磁共振光谱仪实时定量分析活细胞中的代谢通量

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Metabolic reprogramming is widely considered a hallmark of cancer, and understanding metabolic dynamics described by the conversion rates or “fluxes” of metabolites can shed light onto biological processes of tumorigenesis and response to therapy. For real-time analysis of metabolic flux in intact cells or organisms, magnetic resonance (MR) spectroscopy and imaging methods have been developed in conjunction with hyperpolarization of nuclear spins. These approaches enable noninvasive monitoring of tumor progression and treatment efficacy and are being tested in multiple clinical trials. However, because of their limited sensitivity, these methods require a larger number of cells, on the order of 107, which is impractical for analyzing scant target cells or mass-limited samples. We present a new technology platform, a hyperpolarized micromagnetic resonance spectrometer (HMRS), that achieves real-time, 103-fold more sensitive metabolic analysis on live cells. This platform enables quantification of the metabolic flux in a wide range of cell types, including leukemia stem cells, without significant changes in viability, which allows downstream molecular analyses in tandem. It also enables rapid assessment of metabolic changes by a given drug, which may direct therapeutic choices in patients. We further advanced this platform for high-throughput analysis of hyperpolarized molecules by integrating a three-dimensionally printed microfluidic system. The HMRS platform holds promise as a sensitive method for studying metabolic dynamics in mass-limited samples, including primary cancer cells, providing novel therapeutic targets and an enhanced understanding of cellular metabolism.
机译:代谢重编程被广泛认为是癌症的标志,理解由代谢物的转化率或“通量”描述的代谢动力学可以揭示肿瘤发生的生物学过程和对治疗的反应。为了实时分析完整细胞或生物体中的代谢通量,已经开发了磁共振(MR)光谱学和成像方法,并结合了核自旋的超极化作用。这些方法能够无创地监测肿瘤的进展和治疗效果,并且正在多项临床试验中进行测试。但是,由于它们的灵敏度有限,因此这些方法需要大量的细胞,数量级为10 7 ,这对于分析较少的靶细胞或质量受限的样品是不切实际的。我们提出了一种新技术平台,即超极化微磁共振波谱仪(HMRS),该平台可对活细胞进行实时10倍3倍敏感的代谢分析。该平台可对多种类型的细胞(包括白血病干细胞)中的代谢通量进行定量分析,而活力却没有显着变化,从而可以进行下游分子分析。它还可以快速评估给定药物的代谢变化,这可以指导患者的治疗选择。通过集成三维打印的微流体系统,我们进一步改进了该平台,用于超极化分子的高通量分析。 HMRS平台有望成为一种灵敏的方法,用于研究包括原发性癌细胞在内的质量受限样品的代谢动力学,提供新的治疗靶点并增强对细胞代谢的了解。

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