Live isolation of naïve ESCs via distinct glucose metabolism and stored glycogen

Naïve and primed pluripotent stem cells recapitulate the peri- and post-implantation development, respectively. Thus, investigation of distinct traits between each pluripotent stem cell type would shed light on early embryonic processes. Herein, by screening a fluorescent probe library, we found tha...

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Veröffentlicht in:Metabolic engineering 2022-07, Vol.72, p.97-106
Hauptverfasser: Kim, Keun-Tae, Oh, Ji-Young, Park, Seokwoo, Kim, Seong-Min, Benjamin, Patterson, Park, In-Hyun, Chun, Kwang-Hoon, Chang, Young-Tae, Cha, Hyuk-Jin
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Sprache:eng
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Zusammenfassung:Naïve and primed pluripotent stem cells recapitulate the peri- and post-implantation development, respectively. Thus, investigation of distinct traits between each pluripotent stem cell type would shed light on early embryonic processes. Herein, by screening a fluorescent probe library, we found that intracellular glycogen led to specific reactivity to CDg4, a glycogen fluorescence sensor, in both human and mouse naïve embryonic stem cells (ESCs). The requirement of constant inhibition of Gsk3β as well as high oxidative phosphorylation (OxPHOS) in naïve compared to primed ESCs was closely associated to high level of intracellular glycogen in naïve ESCs. Both capacity of OxPHOS and stored glycogen, rescued naïve ESCs by transient inhibition of glycolysis, which selectively eliminated primed ESCs. Additionally, naïve ESCs with active OxPHOS were enriched from a mixture with primed ESCs by high reactivity to ATP-Red1, a mitochondrial ATP fluorescence probe. These results indicate the active OxPHOS and high intracellular glycogen as a novel “biomarker” delineating metabolic remodeling during the transition of naïve pluripotency. •High intracellular glycogen in naïve ESCs upon Gsk3β inhibition.•Live isolation of naïve ESCs from specificity of CDg4 fluorescence probe.•Live isolation of naïve ESCs from ATP-Red1 due to high OxPHOS.•Tolerance of naïve ESCs to temporal inhibition of glycolysis due to distinct glucose metabolism.
ISSN:1096-7176
1096-7184
DOI:10.1016/j.ymben.2022.03.003