Evidence map›Paper›PMID 37865087›Full record

ReviewCell stem cell2023

Hematopoietic stem cells through the ages: A lifetime of adaptation to organismal demands.

Monica Kasbekar, Carl A Mitchell, Melissa A Proven, Emmanuelle Passegué

Abstract readReview
In one paragraph

Review in Cell stem cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
–field-weighted citation impact
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

80 citing papers in PubMed.

  1. Review
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  8. Genetic influences on haematopoiesis.Nature reviews. Genetics · 2026
    Review
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  11. Article
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  19. ATP2B1 expression identifies human hematopoietic stem cells with superior repopulation and self-renewal.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  20. Review

20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Monica KasbekarColumbia Stem Cell Initiative, Department of Genetics and Development, Columbia University, New York, NY 10032, USA; Division of Hematology and Medical Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.
Carl A MitchellColumbia Stem Cell Initiative, Department of Genetics and Development, Columbia University, New York, NY 10032, USA.
Melissa A ProvenColumbia Stem Cell Initiative, Department of Genetics and Development, Columbia University, New York, NY 10032, USA.
Emmanuelle PasseguéColumbia Stem Cell Initiative, Department of Genetics and Development, Columbia University, New York, NY 10032, USA. Electronic address: ep2828@cumc.columbia.edu.

Funding

Emergency Myelopoiesis Pathways in the Control of Blood ProductionR35HL135763 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PASSEGUE, EMMANUELLE · 2017 to 2023
$5.7M
New York Consortium for Interdisciplinary Training in Kidney, Urological and Hematological Research (NYC Train KUHR)TL1DK136048 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI JONATHAN M. BARASCH, Wadie F Bahou · 2022 to 2026
$3.8M
Mechanisms of Hematopoietic Stem Cell and Blood agingR01AG073599 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PASSEGUE, EMMANUELLE · 2021 to 2025
$2.5M
Replication Stress and Ribosome Biogenesis in Hematopoietic Stem Cell AgingF31HL160207 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MITCHELL, CARL · 2021 to 2023
$136k
NHLBI NIH HHS F31 HL160207NHLBI NIH HHS R35 HL135763NIA NIH HHS R01 AG073599NIDDK NIH HHS TL1 DK136048
6 · The paper itself

Abstract

Hematopoietic stem cells (HSCs), which govern the production of all blood lineages, transition through a series of functional states characterized by expansion during fetal development, functional quiescence in adulthood, and decline upon aging. We describe central features of HSC regulation during ontogeny to contextualize how adaptive responses over the life of the organism ultimately form the basis for HSC functional degradation with age. We particularly focus on the role of cell cycle regulation, inflammatory response pathways, epigenetic changes, and metabolic regulation. We then explore how the knowledge of age-related changes in HSC regulation can inform strategies for the rejuvenation of old HSCs.

Indexed as

Epigenesis, GeneticHematopoietic Stem Cellsagingdevelopmentepigenetichematopoietic stem cellsinflammationmetabolismniche regulationquiescencerejuvenation

Identifiers

PMID37865087
PMCPMC10842631

What OpenQuestion holds

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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.