Go to JCI Insight
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Alerts
  • Advertising/recruitment
  • Subscribe
  • Contact
  • Current Issue
  • Past Issues
  • By specialty
    • COVID-19
    • Cardiology
    • Gastroenterology
    • Immunology
    • Metabolism
    • Nephrology
    • Neuroscience
    • Oncology
    • Pulmonology
    • Vascular biology
    • All ...
  • Videos
    • Conversations with Giants in Medicine
    • Author's Takes
  • Reviews
    • View all reviews ...
    • 100th Anniversary of Insulin's Discovery (Jan 2021)
    • Hypoxia-inducible factors in disease pathophysiology and therapeutics (Oct 2020)
    • Latency in Infectious Disease (Jul 2020)
    • Immunotherapy in Hematological Cancers (Apr 2020)
    • Big Data's Future in Medicine (Feb 2020)
    • Mechanisms Underlying the Metabolic Syndrome (Oct 2019)
    • Reparative Immunology (Jul 2019)
    • View all review series ...
  • Viewpoint
  • Collections
    • Recently published
    • In-Press Preview
    • Commentaries
    • Concise Communication
    • Editorials
    • Viewpoint
    • Top read articles
  • Clinical Medicine
  • JCI This Month
    • Current issue
    • Past issues

  • Current issue
  • Past issues
  • Specialties
  • Reviews
  • Review series
  • Conversations with Giants in Medicine
  • Author's Takes
  • Recently published
  • In-Press Preview
  • Commentaries
  • Concise Communication
  • Editorials
  • Viewpoint
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Alerts
  • Advertising/recruitment
  • Subscribe
  • Contact
Top
  • View PDF
  • Download citation information
  • Send a letter
  • Share this article
  • Terms of use
  • Standard abbreviations
  • Need Help? E-mail the JCI
  • Top
  • Abstract
  • Supplemental material
  • Version history
  • Article usage
  • Citations to this article

Advertisement

ResearchIn-Press PreviewHematologyStem cells Free access | 10.1172/JCI131698

Concerted roles of PTEN and ATM in controlling hematopoietic stem cell fitness and dormancy

Jerome Fortin,1 Christian Bassi,1 Parameswaran Ramachandran,1 Wanda Y. Li,1 Ruxiao Tian,1 Ida Zarrabi,1 Graham Hill,1 Bryan E. Snow,1 Jillian Haight,1 Chantal Tobin,1 Kelsey Hodgson,1 Andrew Wakeham,1 Vuk Stambolic,2 and Tak W. Mak1

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Fortin, J. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Bassi, C. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Ramachandran, P. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Li, W. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Tian, R. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Zarrabi, I. in: JCI | PubMed | Google Scholar |

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Hill, G. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Snow, B. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Haight, J. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Tobin, C. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Hodgson, K. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Wakeham, A. in: JCI | PubMed | Google Scholar

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Stambolic, V. in: JCI | PubMed | Google Scholar |

1Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

2Department of Medical Biophysics, University of Toronto, Toronto, Canada

Find articles by Mak, T. in: JCI | PubMed | Google Scholar

Published January 14, 2021 - More info

J Clin Invest. https://doi.org/10.1172/JCI131698.
Copyright © 2021, American Society for Clinical Investigation
Published January 14, 2021 - Version history
View PDF
Abstract

In order to sustain proficient life-long hematopoiesis, hematopoietic stem cells (HSCs) must possess robust mechanisms to preserve their quiescence and genome integrity. DNA-damaging stress can perturb HSC homeostasis by affecting their survival, self-renewal and differentiation. Ablation of the kinase ATM, a master regulator of the DNA damage response, impairs HSC fitness. Paradoxically, we show here that loss of a single allele of Atm enhances HSC functionality in mice. To explain this observation, we explored a possible link between ATM and the tumor suppressor PTEN, which also regulates HSC function. We generated and analyzed a knock-in mouse line (PtenS398A/S398A), in which PTEN cannot be phosphorylated by ATM. Similar to Atm+/-, PtenS398A/S398A HSCs have enhanced hematopoietic reconstitution ability, accompanied by resistance to apoptosis induced by genotoxic stress. Single-cell transcriptomic analyses and functional assays revealed that dormant PtenS398A/S398A HSCs aberrantly tolerate elevated mitochondrial activity and the accumulation of reactive oxygen species, which are normally associated with HSC priming for self-renewal or differentiation. Our results unveil a molecular connection between ATM and PTEN, which couples the response to genotoxic stress and dormancy in HSC.

Graphical Abstract
graphical abstract
Supplemental material

View

Version history
  • Version 1 (January 14, 2021): In-Press Preview

Article tools

  • View PDF
  • Download citation information
  • Send a letter
  • Share this article
  • Terms of use
  • Standard abbreviations
  • Need Help? E-mail the JCI

Metrics

  • Article usage
  • Citations to this article

Go to

  • Top
  • Abstract
  • Supplemental material
  • Version history
Advertisement
Advertisement
Follow JCI:
Copyright © 2021 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

Sign up for email alerts