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

机译:测量能量代谢中培养的细胞包括人多能干细胞和分化的细胞

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摘要

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:需要测量糖酵解和线粒体功能,以量化各种细胞环境中的能量代谢。在人多能干细胞(HPSC)及其分化的后代,这种分析可能是挑战,因为细胞性质,生长条件和维持这些细胞类型所需的费用。在这里,我们提供用于分析HPSC中的能量代谢的协议及其通常适用于成熟细胞类型的早期分化的子种。我们的方法揭示了HPSC,分化细胞,各种癌细胞和rhO - 零细胞使用的不同能量代谢谱。方案根据细胞外酸化速率测量或估计糖酵解,并根据氧气消耗率测量或估计氧化磷酸化。测定通常需要3小时过夜样品制备。还讨论并提供了伴侣方法,以帮助研究人员在开发更复杂的细胞生物生物终体植物的延长分析的更复杂的实验方案方面。

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