Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/15535
Title: Energy Metabolism in Human Pluripotent Stem Cells and Their Differentiated Counterparts
Authors: Varum, Sandra 
Rodrigues, Ana S. 
Moura, Michelle B. 
Momcilovic, Olga 
Easley, Charles A. 
Ramalho-Santos, João 
Van Houten, Bennett 
Schatten, Gerald 
Issue Date: 17-Jun-2011
Publisher: Public Library of Science
Citation: VARUM, Sandra [et al.] - Energy Metabolism in Human Pluripotent Stem Cells and Their Differentiated Counterparts. "PLoS ONE" [em linha]. Vol. 6, nº 6 (2011) e20914. [Consult. Dia Mês Ano]. Disponível em WWW:<http://hdl.handle.net/10316/15535>. ISSN 1932-6203
Serial title, monograph or event: PLoS ONE
Volume: 6
Issue: 6
Abstract: Background: Human pluripotent stem cells have the ability to generate all cell types present in the adult organism, therefore harboring great potential for the in vitro study of differentiation and for the development of cell-based therapies. Nonetheless their use may prove challenging as incomplete differentiation of these cells might lead to tumoregenicity. Interestingly, many cancer types have been reported to display metabolic modifications with features that might be similar to stem cells. Understanding the metabolic properties of human pluripotent stem cells when compared to their differentiated counterparts can thus be of crucial importance. Furthermore recent data has stressed distinct features of different human pluripotent cells lines, namely when comparing embryo-derived human embryonic stem cells (hESCs) and induced pluripotent stem cells (IPSCs) reprogrammed from somatic cells. Methodology/Principal Findings: We compared the energy metabolism of hESCs, IPSCs, and their somatic counterparts. Focusing on mitochondria, we tracked organelle localization and morphology. Furthermore we performed gene expression analysis of several pathways related to the glucose metabolism, including glycolysis, the pentose phosphate pathway and the tricarboxylic acid (TCA) cycle. In addition we determined oxygen consumption rates (OCR) using a metabolic extracellular flux analyzer, as well as total intracellular ATP levels by high performance liquid chromatography (HPLC). Finally we explored the expression of key proteins involved in the regulation of glucose metabolism. Conclusions/Findings: Our results demonstrate that, although the metabolic signature of IPSCs is not identical to that of hESCs, nonetheless they cluster with hESCs rather than with their somatic counterparts. ATP levels, lactate production and OCR revealed that human pluripotent cells rely mostly on glycolysis to meet their energy demands. Furthermore, our work points to some of the strategies which human pluripotent stem cells may use to maintain high glycolytic rates, such as high levels of hexokinase II and inactive pyruvate dehydrogenase (PDH).
URI: http://hdl.handle.net/10316/15535
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0020914
Rights: openAccess
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
FCTUC Ciências da Vida - Artigos em Revistas Internacionais

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