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Measuring energy metabolism in cultured cells, including human pluripotent stem cells and differentiated cells

机译:测量培养细胞(包括人多能干细胞和分化细胞)中的能量代谢

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Measurements of glycolysis and mitochondrial function are required to quantify energy metabolism in a wide variety of cellular contexts. In human pluripotent stem cells (hPSCs) and their differentiated progeny, this analysis can be challenging because of the unique cell properties, growth conditions and expense required to maintain these cell types. Here we provide protocols for analyzing energy metabolism in hPSCs and their early differentiated progenies that are generally applicable to mature cell types as well. Our approach has revealed distinct energy metabolism profiles used by hPSCs, differentiated cells, a variety of cancer cells and Rho-null cells. The protocols measure or estimate glycolysis on the basis of the extracellular acidification rate, and they measure or estimate oxidative phosphorylation on the basis of the oxygen consumption rate. Assays typically require 3 h after overnight sample preparation. Companion methods are also discussed and provided to aid researchers in developing more sophisticated experimental regimens for extended analyses of cellular bioenergetics.
机译:需要糖酵解和线粒体功能的测量以量化在各种细胞环境中的能量代谢。在人类多能干细胞(hPSC)及其分化后代中,由于独特的细胞特性,生长条件和维持这些细胞类型所需的费用,该分析可能具有挑战性。在这里,我们提供了用于分析hPSC及其早期分化后代中能量代谢的协议,这些协议通常也适用于成熟细胞类型。我们的方法揭示了hPSC,分化细胞,多种癌细胞和Rho-null细胞所使用的独特能量代谢谱。该方案基于细胞外酸化率来测量或估计糖酵解,并且基于氧消耗率来测量或估计氧化磷酸化。过夜样品制备后通常需要3小时进行测定。还讨论并提供了同伴方法,以帮助研究人员开发更复杂的实验方案,以进行细胞生物能学的扩展分析。

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