Evidence map›Paper›PMID 38402617›Full record

ArticleCell stem cell2024

An iron rheostat controls hematopoietic stem cell fate.

Yun-Ruei Kao, Jiahao Chen, Rajni Kumari, Anita Ng, Aliona Zintiridou, Madhuri Tatiparthy, Yuhong Ma, Maria M Aivalioti, Deeposree Moulik, Sriram Sundaravel and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Cell stem cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
11.8field-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

31 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Paracrine iron activates HopxJournal of advanced research · 2026
    Article
  3. Review
  4. Article
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  7. Article
  8. Review
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  12. Review
  13. Article
  14. Article
  15. Iron and the immune system.Nature reviews. Immunology · 2025
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

20 authors at 4 institutions in 1 country.

Yun-Ruei KaoDepartment of Oncology, Albert Einstein College of Medicine, New York, NY, USA. Electronic address: yun-ruei.kao@einsteinmed.edu.
Jiahao ChenDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Rajni KumariDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Anita NgKarches Center for Oncology Research, the Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY, USA.
Aliona ZintiridouDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Madhuri TatiparthyDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Yuhong MaDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Maria M AivaliotiDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Deeposree MoulikDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Sriram SundaravelDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Daqian SunDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Julie A ReiszDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Juliane GrimmDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Nuria Martinez-LopezDepartment of Medicine, University of California, Los Angeles, Los Angeles, CA, USA; Vatche and Tamar Manoukian Division of Digestive Diseases, University of California, Los Angeles, Los Angeles, CA, USA; Comprehensive Liver Research Center at University of California Los Angeles, CA, USA.
Stephanie StranskyDepartment of Biochemistry, Albert Einstein College of Medicine, New York, NY, USA.
Simone SidoliDepartment of Biochemistry, Albert Einstein College of Medicine, New York, NY, USA.
Ulrich SteidlDepartment of Oncology, Albert Einstein College of Medicine, New York, NY, USA; Department of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA; Ruth L. and David S. Gottesman Institute for Stem Cell Research and Regenerative Medicine, Albert Einstein College of Medicine, New York, NY, USA; Blood Cancer Institute, Montefiore Einstein Comprehensive Cancer Center, Albert Einstein College of Medicine, Bronx, NY, USA; Cancer Dormancy and Tumor Microenvironment Institute, Montefiore Einstein Comprehensive Cancer Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Rajat SinghDepartment of Medicine, University of California, Los Angeles, Los Angeles, CA, USA; Vatche and Tamar Manoukian Division of Digestive Diseases, University of California, Los Angeles, Los Angeles, CA, USA; Comprehensive Liver Research Center at University of California Los Angeles, CA, USA.
Angelo D'AlessandroDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Britta WillDepartment of Oncology, Albert Einstein College of Medicine, New York, NY, USA; Department of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA; Ruth L. and David S. Gottesman Institute for Stem Cell Research and Regenerative Medicine, Albert Einstein College of Medicine, New York, NY, USA; Blood Cancer Institute, Montefiore Einstein Comprehensive Cancer Center, Albert Einstein College of Medicine, Bronx, NY, USA; Cancer Dormancy and Tumor Microenvironment Institute, Montefiore Einstein Comprehensive Cancer Center, Albert Einstein College of Medicine, Bronx, NY, USA; Institute for Aging Studies, Albert Einstein College of Medicine, New York, NY, USA. Electronic address: britta.will@einsteinmed.edu.
Albert Einstein College of Medicine · USUniversity of California, Los Angeles · USUniversity of Colorado Anschutz Medical Campus · USNorthwell Health · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI STEVEN C. ALMO · 1985 to 2026
$111.2M
The Impact of Oxidative Stress on Erythocyte BiologyR01HL148151 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI D'ALESSANDRO, ANGELO, KARAFIN, MATTHEW S · 2019 to 2022
$8.9M
Training in Aging ResearchT32AG023475 · NIA · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI NIR J BARZILAI, DEREK Major HUFFMAN · 2004 to 2026
$8.6M
Molecular and Cellular Regulation of Pre-Leukemic Stem Cells and their Therapeutic TargetingR35CA253127 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Ulrich Steidl · 2021 to 2026
$5.6M
The role of ferroptosis in red cell aging in vivo and in vitroR01HL146442 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Angelo D'Alessandro, Adam N. Goldfarb · 2019 to 2026
$5.4M
Identification and targeting of pathways separating healthy stem cell aging from malignant transformationR01CA230756 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Britta Will · 2018 to 2026
$4.0M
Contribution of macrophages in the HSC nicheR01HL157948 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI STEIDL, ULRICH, WILL, BRITTA · 2021 to 2024
$2.2M
Hyptothalamic autophagy and metabolic regulation in agingRF1AG043517 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SINGH, RAJAT · 2019 to 2019
$2.1M
Molecular regulation of gut lipid metabolism by mTOR and autophagy proteinsR01DK123327 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SINGH, RAJAT · 2019 to 2023
$1.9M
Leveraging epigenetic and epitranscriptomic aberrations in cancer to identify molecular targets for designing therapyK00CA223044 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SUNDARAVEL, SRIRAM · 2019 to 2022
$379k
NCI NIH HHS K00 CA223044NCI NIH HHS P30 CA013330NCI NIH HHS R01 CA230756NCI NIH HHS R35 CA253127NHLBI NIH HHS R01 HL146442NHLBI NIH HHS R01 HL148151NHLBI NIH HHS R01 HL157948NIA NIH HHS RF1 AG043517NIA NIH HHS T32 AG023475NIDDK NIH HHS R01 DK123327
6 · The paper itself

Abstract

Mechanisms governing the maintenance of blood-producing hematopoietic stem and multipotent progenitor cells (HSPCs) are incompletely understood, particularly those regulating fate, ensuring long-term maintenance, and preventing aging-associated stem cell dysfunction. We uncovered a role for transitory free cytoplasmic iron as a rheostat for adult stem cell fate control. We found that HSPCs harbor comparatively small amounts of free iron and show the activation of a conserved molecular response to limited iron-particularly during mitosis. To study the functional and molecular consequences of iron restriction, we developed models allowing for transient iron bioavailability limitation and combined single-molecule RNA quantification, metabolomics, and single-cell transcriptomic analyses with functional studies. Our data reveal that the activation of the limited iron response triggers coordinated metabolic and epigenetic events, establishing stemness-conferring gene regulation. Notably, we find that aging-associated cytoplasmic iron loading reversibly attenuates iron-dependent cell fate control, explicating intervention strategies for dysfunctional aged stem cells.

Indexed as

HematopoiesisIronCell DifferentiationGene Expression RegulationHematopoietic Stem CellsMultipotent Stem CellsIronaginggene regulationhematopoiesisironmetabolismstem cellsTip60/KAT5

Identifiers

PMID38402617
PMCPMC10939794
OpenAlexW4392059717

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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.