| Literature DB >> 26059508 |
Hyunsoo Kim1, Hyonchol Jang1,2, Tae Wan Kim1, Byung-Hee Kang1, Sang Eun Lee3, Yoon Kyung Jeon1,4, Doo Hyun Chung1,4, Jinmi Choi1, Jihoon Shin1, Eun-Jung Cho5, Hong-Duk Youn1,6.
Abstract
Pluripotent stem cells (PSCs) have distinct metabolic properties that support their metabolic and energetic needs and affect their stemness. In particular, high glycolysis is critical for the generation and maintenance of PSCs. However, it is unknown how PSCs maintain and acquire this metabolic signature. In this study, we found that core pluripotency factors regulate glycolysis directly by controlling the expression of glycolytic enzymes. Specifically, Oct4 directly governs Hk2 and Pkm2, which are important glycolytic enzymes that determine the rate of glycolytic flux. The overexpression of Hk2 and Pkm2 sustains high levels of glycolysis during embryonic stem cell (ESC) differentiation. Moreover, the maintenance of high glycolysis levels by Hk2 and Pkm2 overexpression hampers differentiation and preserves the pluripotency of ESCs in the absence of leukemia inhibitory factor. Overall, our study identifies a direct molecular connection between core pluripotency factors and ESC metabolic signatures and demonstrates the significance of metabolism in cell fate determination.Entities:
Keywords: Core pluripotency factors; Embryonic stem cells; Glycolysis; Hexokinase 2; Metabolism; Oct4; Pyruvate kinase M2
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Year: 2015 PMID: 26059508 DOI: 10.1002/stem.2073
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277