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Metabolism of Stem and Progenitor Cells: Proper Methods to Answer Specific Questions

机译:干细胞和祖细胞的代谢:回答特定问题的正确方法

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摘要

Stem cells can stay quiescent for a long period of time or proliferate and differentiate into multiple lineages. The activity of stage-specific metabolic programs allows stem cells to best adapt their functions in different microenvironments. Specific cellular phenotypes can be, therefore, defined by precise metabolic signatures. Notably, not only cellular metabolism describes a defined cellular phenotype, but experimental evidence now clearly indicate that also rewiring cells towards a particular cellular metabolism can drive their cellular phenotype and function accordingly. Cellular metabolism can be studied by both targeted and untargeted approaches. Targeted analyses focus on a subset of identified metabolites and on their metabolic fluxes. In addition, the overall assessment of the oxygen consumption rate (OCR) gives a measure of the overall cellular oxidative metabolism and mitochondrial function. Untargeted approach provides a large-scale identification and quantification of the whole metabolome with the aim to describe a metabolic fingerprinting. In this review article, we overview the methodologies currently available for the study of in vitro stem cell metabolism, including metabolic fluxes, fingerprint analyses, and single-cell metabolomics. Moreover, we summarize available approaches for the study of in vivo stem cell metabolism. For all of the described methods, we highlight their specificities and limitations. In addition, we discuss practical concerns about the most threatening steps, including metabolic quenching, sample preparation and extraction. A better knowledge of the precise metabolic signature defining specific cell population is instrumental to the design of novel therapeutic strategies able to drive undifferentiated stem cells towards a selective and valuable cellular phenotype.
机译:干细胞可以长时间保持静止或增殖并分化为多个谱系。特定阶段代谢程序的活动使干细胞能够在不同的微环境中最佳地适应其功能。因此,特定的细胞表型可以通过精确的代谢特征来定义。值得注意的是,不仅细胞代谢描述了确定的细胞表型,而且现在的实验证据清楚地表明,将细胞重新导向特定的细胞代谢也可以驱动其细胞表型并相应地起作用。可以通过靶向和非靶向方法研究细胞代谢。靶向分析的重点是已识别代谢物的子集及其代谢通量。此外,对耗氧率(OCR)的总体评估可以衡量整体细胞的氧化代谢和线粒体功能。非靶向方法可对整个代谢组进行大规模鉴定和定量,以描述代谢指纹图谱。在这篇综述文章中,我们概述了目前可用于体外干细胞代谢研究的方法,包括代谢通量,指纹分析和单细胞代谢组学。此外,我们总结了体内干细胞代谢研究的可用方法。对于所有上述方法,我们重点介绍了它们的特殊性和局限性。此外,我们讨论了有关最具威胁性步骤的实际问题,包括代谢猝灭,样品制备和提取。对定义特定细胞群的精确代谢特征的更好了解有助于设计新的治疗策略,该策略能够将未分化的干细胞推向选择性和有价值的细胞表型。

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