Lane Andrew N, Higashi Richard M, Fan Teresa W-M
Department of Toxicology and Cancer Biology and Markey Cancer Center, University of Kentucky, 789 S. Limestone St., Lexington, KY 40536, USA.
Metabolites. 2024 Jul 11;14(7):383. doi: 10.3390/metabo14070383.
Stable isotope-resolved metabolomics comprises a critical set of technologies that can be applied to a wide variety of systems, from isolated cells to whole organisms, to define metabolic pathway usage and responses to perturbations such as drugs or mutations, as well as providing the basis for flux analysis. As the diversity of stable isotope-enriched compounds is very high, and with newer approaches to multiplexing, the coverage of metabolism is now very extensive. However, as the complexity of the model increases, including more kinds of interacting cell types and interorgan communication, the analytical complexity also increases. Further, as studies move further into spatially resolved biology, new technical problems have to be overcome owing to the small number of analytes present in the confines of a single cell or cell compartment. Here, we review the overall goals and solutions made possible by stable isotope tracing and their applications to models of increasing complexity. Finally, we discuss progress and outstanding difficulties in high-resolution spatially resolved tracer-based metabolic studies.
稳定同位素分辨代谢组学包含一系列关键技术,这些技术可应用于从分离细胞到整个生物体等各种各样的系统,以确定代谢途径的使用情况以及对诸如药物或突变等扰动的反应,并为通量分析提供基础。由于富含稳定同位素的化合物种类繁多,且随着多重分析的新方法出现,目前代谢的覆盖范围非常广泛。然而,随着模型复杂性的增加,包括更多种类的相互作用细胞类型和器官间通讯,分析的复杂性也随之增加。此外,随着研究进一步深入到空间分辨生物学领域,由于单个细胞或细胞区室范围内存在的分析物数量较少,必须克服新的技术问题。在此,我们综述了稳定同位素示踪所实现的总体目标和解决方案及其在日益复杂模型中的应用。最后,我们讨论了基于示踪剂的高分辨率空间分辨代谢研究的进展和突出困难。