Back to Search Start Over

FoxO maintains a genuine muscle stem-cell quiescent state until geriatric age

Authors :
Stephen R. Brooks
Hong-Wei Sun
Vittorio Sartorelli
Kan Jiang
Marco Sandri
Laura Ortet
Stefania Dell'Orso
Srikanth Ravichandran
Sonia Alonso-Martin
Aster H. Juan
Laura García-Prat
Victoria Moiseeva
Marta Flández
Eusebio Perdiguero
Vanessa Ruiz-Bonilla
Pura Muñoz-Cánoves
Elena Rebollo
Mercè Jardí
Antonio Musarò
Xiaotong Hong
Antonio del Sol
Silvia Campanario
Ministerio de Economía y Competitividad (España)
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
European Commission
Foundation for the National Institutes of Health
Fundación Severo Ochoa
Source :
Nature Cell Biology, Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2020
Publisher :
Springer Science and Business Media LLC, 2020.

Abstract

Tissue regeneration declines with ageing but little is known about whether this arises from changes in stem-cell heterogeneity. Here, in homeostatic skeletal muscle, we identify two quiescent stem-cell states distinguished by relative CD34 expression: CD34High, with stemness properties (genuine state), and CD34Low, committed to myogenic differentiation (primed state). The genuine-quiescent state is unexpectedly preserved into later life, succumbing only in extreme old age due to the acquisition of primed-state traits. Niche-derived IGF1-dependent Akt activation debilitates the genuine stem-cell state by imposing primed-state features via FoxO inhibition. Interventions to neutralize Akt and promote FoxO activity drive a primed-to-genuine state conversion, whereas FoxO inactivation deteriorates the genuine state at a young age, causing regenerative failure of muscle, as occurs in geriatric mice. These findings reveal transcriptional determinants of stem-cell heterogeneity that resist ageing more than previously anticipated and are only lost in extreme old age, with implications for the repair of geriatric muscle.<br />The authors acknowledge funding from MINECO-Spain (grant no. RTI2018-096068), ERC2016-AdG-741966, LaCaixa-HEALTH-HR17-00040, MDA, UPGRADE-H2020-825825, AFM and DPP-Spain to P.M.-C; María-de-Maeztu-Program for Units of Excellence to UPF (grant no. MDM-2014-0370) and the Severo-Ochoa-Program for Centers of Excellence to CNIC (grant no. SEV-2015-0505). This work was also supported by NIAMS IRP through NIH grants nos AR041126 and AR041164 to V.S. and utilized computational resources of the NIH HPC Biowulf cluster (http://hpc.nih.gov); ASI, Ricerca Finalizzata, Ateneo Sapienza to A.M.; AIRC (grant no. 23257); ASI (grant no. MARS-PRE, DC-VUM-2017-006); H2020-MSCA-RISE-2014 (645648) to M.S. and a FNR core grant (grant no. C15/BM/10397420) to A.d.S. L.G.P. was partially supported by an FPI fellowship and an EMBO fellowship (grant no. ALTF 420-2017); and S.C., X.H. and V.M. by FI, Severo-Ochoa and PFI Fellowships (Spain), respectively.

Details

ISSN :
14764679 and 14657392
Volume :
22
Database :
OpenAIRE
Journal :
Nature Cell Biology
Accession number :
edsair.doi.dedup.....9bd712fed7a626160dc61b98ee2ae203
Full Text :
https://doi.org/10.1038/s41556-020-00593-7