Suppression of SIRT2 and altered acetylation status of human pluripotent stem cells: possible link to metabolic switch during reprogramming.

Abstract:

:Primed human pluripotent stem cells (hPSCs) are highly dependent on glycolysis rather than oxidative phosphorylation, which is similar to the metabolic switch that occurs in cancer cells. However, the molecular mechanisms that underlie this metabolic reprogramming in hPSCs and its relevance to pluripotency remain unclear. Cha et al. (2017) recently revealed that downregulation of SIRT2 by miR-200c enhances acetylation of glycolytic enzymes and glycolysis, which in turn facilitates cellular reprogramming, suggesting that SIRT2 is a key enzyme linking the metabolic switch and pluripotency in hPSCs. [BMB Reports 2017; 50(9): 435-436].

journal_name

BMB Rep

journal_title

BMB reports

authors

Kwon OS,Han MJ,Cha HJ

doi

10.5483/bmbrep.2017.50.9.119

subject

Has Abstract

pub_date

2017-09-01 00:00:00

pages

435-436

issue

9

eissn

1976-6696

issn

1976-670X

pii

3906

journal_volume

50

pub_type

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