Evidence map›Paper›PMID 28802040›Full record

ArticleCell2017

Aged Stem Cells Reprogram Their Daily Rhythmic Functions to Adapt to Stress.

Guiomar Solanas, Francisca Oliveira Peixoto, Eusebio Perdiguero, Mercè Jardí, Vanessa Ruiz-Bonilla, Debayan Datta, Aikaterini Symeonidi, Andrés Castellanos, Patrick-Simon Welz, Juan Martín Caballero and 3 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed
10.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

145 citing papers in PubMed, 230 citations in OpenAlex.

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  11. NADCommunications biology · 2026
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85 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 2 countries.

Guiomar SolanasInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain.
Francisca Oliveira PeixotoInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain.
Eusebio PerdigueroUniversitat Pompeu Fabra (UPF), Department of Experimental and Health Sciences (DCEXS) and CIBER on Neurodegenerative Diseases (CIBERNED), 08003 Barcelona, Spain.
Mercè JardíUniversitat Pompeu Fabra (UPF), Department of Experimental and Health Sciences (DCEXS) and CIBER on Neurodegenerative Diseases (CIBERNED), 08003 Barcelona, Spain.
Vanessa Ruiz-BonillaUniversitat Pompeu Fabra (UPF), Department of Experimental and Health Sciences (DCEXS) and CIBER on Neurodegenerative Diseases (CIBERNED), 08003 Barcelona, Spain.
Debayan DattaInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain.
Aikaterini SymeonidiInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain.
Andrés CastellanosInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain.
Patrick-Simon WelzInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain.
Juan Martín CaballeroPCB-PRBB Animal Facilities, 08028 Barcelona, Spain.
Paolo Sassone-CorsiCenter for Epigenetics and Metabolism, University of California, Irvine, CA 92607, USA.
Pura Muñoz-CánovesICREA, Catalan Institution for Research and Advanced Studies, 08010 Barcelona, Spain; Universitat Pompeu Fabra (UPF), Department of Experimental and Health Sciences (DCEXS) and CIBER on Neurodegenerative Diseases (CIBERNED), 08003 Barcelona, Spain; Spanish National Center for Cardiovascular Research (CNIC), 28029 Madrid, Spain. Electronic address: pura.munoz@upf.edu.
Salvador Aznar BenitahInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain; ICREA, Catalan Institution for Research and Advanced Studies, 08010 Barcelona, Spain. Electronic address: salvador.aznar-benitah@irbbarcelona.org.
Institute for Research in Biomedicine · ESBiomedical Research Networking Center on Neurodegenerative Diseases · ESPompeu Fabra University · ESBarcelona Biomedical Research Park · ESUniversity of California, Irvine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Normal homeostatic functions of adult stem cells have rhythmic daily oscillations that are believed to become arrhythmic during aging. Unexpectedly, we find that aged mice remain behaviorally circadian and that their epidermal and muscle stem cells retain a robustly rhythmic core circadian machinery. However, the oscillating transcriptome is extensively reprogrammed in aged stem cells, switching from genes involved in homeostasis to those involved in tissue-specific stresses, such as DNA damage or inefficient autophagy. Importantly, deletion of circadian clock components did not reproduce the hallmarks of this reprogramming, underscoring that rewiring, rather than arrhythmia, is associated with physiological aging. While age-associated rewiring of the oscillatory diurnal transcriptome is not recapitulated by a high-fat diet in young adult mice, it is significantly prevented by long-term caloric restriction in aged mice. Thus, stem cells rewire their diurnal timed functions to adapt to metabolic cues and to tissue-specific age-related traits.

Indexed as

Cellular SenescenceCircadian RhythmAdult Stem CellsAnimalsAutophagyCaloric RestrictionCircadian ClocksDiet, High-FatDNA DamageEpidermisHomeostasisMiceMuscle, SkeletalStress, PhysiologicalTranscriptomeagingcaloric restrictioncircadian reprogrammingCircadian rhythmsdietepidermal stem cellshallmarks of aginghigh fat dietmuscle stem cells (satellite cells)stem cells

Identifiers

PMID28802040
OpenAlexW2744641317

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.