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Specification of haematopoietic stem cell fate via modulation of mitochondrial activity

Haematopoietic stem cells (HSCs) differ from their committed progeny by relying primarily on anaerobic glycolysis rather than mitochondrial oxidative phosphorylation for energy production. However, whether this change in the metabolic program is the cause or the consequence of the unique function of...

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Autores principales: Vannini, Nicola, Girotra, Mukul, Naveiras, Olaia, Nikitin, Gennady, Campos, Vasco, Giger, Sonja, Roch, Aline, Auwerx, Johan, Lutolf, Matthias P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064016/
https://www.ncbi.nlm.nih.gov/pubmed/27731316
http://dx.doi.org/10.1038/ncomms13125
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author Vannini, Nicola
Girotra, Mukul
Naveiras, Olaia
Nikitin, Gennady
Campos, Vasco
Giger, Sonja
Roch, Aline
Auwerx, Johan
Lutolf, Matthias P.
author_facet Vannini, Nicola
Girotra, Mukul
Naveiras, Olaia
Nikitin, Gennady
Campos, Vasco
Giger, Sonja
Roch, Aline
Auwerx, Johan
Lutolf, Matthias P.
author_sort Vannini, Nicola
collection PubMed
description Haematopoietic stem cells (HSCs) differ from their committed progeny by relying primarily on anaerobic glycolysis rather than mitochondrial oxidative phosphorylation for energy production. However, whether this change in the metabolic program is the cause or the consequence of the unique function of HSCs remains unknown. Here we show that enforced modulation of energy metabolism impacts HSC self-renewal. Lowering the mitochondrial activity of HSCs by chemically uncoupling the electron transport chain drives self-renewal under culture conditions that normally induce rapid differentiation. We demonstrate that this metabolic specification of HSC fate occurs through the reversible decrease of mitochondrial mass by autophagy. Our data thus reveal a causal relationship between mitochondrial metabolism and fate choice of HSCs and also provide a valuable tool to expand HSCs outside of their native bone marrow niches.
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spelling pubmed-50640162016-10-26 Specification of haematopoietic stem cell fate via modulation of mitochondrial activity Vannini, Nicola Girotra, Mukul Naveiras, Olaia Nikitin, Gennady Campos, Vasco Giger, Sonja Roch, Aline Auwerx, Johan Lutolf, Matthias P. Nat Commun Article Haematopoietic stem cells (HSCs) differ from their committed progeny by relying primarily on anaerobic glycolysis rather than mitochondrial oxidative phosphorylation for energy production. However, whether this change in the metabolic program is the cause or the consequence of the unique function of HSCs remains unknown. Here we show that enforced modulation of energy metabolism impacts HSC self-renewal. Lowering the mitochondrial activity of HSCs by chemically uncoupling the electron transport chain drives self-renewal under culture conditions that normally induce rapid differentiation. We demonstrate that this metabolic specification of HSC fate occurs through the reversible decrease of mitochondrial mass by autophagy. Our data thus reveal a causal relationship between mitochondrial metabolism and fate choice of HSCs and also provide a valuable tool to expand HSCs outside of their native bone marrow niches. Nature Publishing Group 2016-10-12 /pmc/articles/PMC5064016/ /pubmed/27731316 http://dx.doi.org/10.1038/ncomms13125 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Vannini, Nicola
Girotra, Mukul
Naveiras, Olaia
Nikitin, Gennady
Campos, Vasco
Giger, Sonja
Roch, Aline
Auwerx, Johan
Lutolf, Matthias P.
Specification of haematopoietic stem cell fate via modulation of mitochondrial activity
title Specification of haematopoietic stem cell fate via modulation of mitochondrial activity
title_full Specification of haematopoietic stem cell fate via modulation of mitochondrial activity
title_fullStr Specification of haematopoietic stem cell fate via modulation of mitochondrial activity
title_full_unstemmed Specification of haematopoietic stem cell fate via modulation of mitochondrial activity
title_short Specification of haematopoietic stem cell fate via modulation of mitochondrial activity
title_sort specification of haematopoietic stem cell fate via modulation of mitochondrial activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064016/
https://www.ncbi.nlm.nih.gov/pubmed/27731316
http://dx.doi.org/10.1038/ncomms13125
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